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Low-dose naltrexone benefits include fighting inflammation, oxidative stress, and cancer, modulating immune function, treating autoimmune conditions and chronic pain, reducing insulin resistance, and improving skin health. Its multifaceted action makes it a promising treatment for various chronic conditions.
High-dose naltrexone benefits include promoting weight loss, aiding smoking cessation, and treating impulse control disorders, chronic pain, alcohol dependence, and opioid addiction by blocking opioid receptors and reducing cravings and withdrawal symptoms. It also helps regulate addictive behaviors and supports overall recovery.
Naltrexone is a drug used to treat alcoholism and opioid addiction. It belongs to a group of drugs called opioid antagonists, which work by blocking the effect of opioid receptors and dramatically reducing cravings and urges to drink alcohol or take opioids. Along with counseling and other support, naltrexone treatment allows patients to maintain abstinence, reduce the harms related to the use of these substances, and improve their quality of life. The length of the treatment greatly depends on each patient’s needs and situation.
Low-dose naltrexone (LDN) works by temporarily blocking opioid receptors in the body, leading to a rebound effect that increases the production of endogenous opioids, such as endorphins. This increase in endorphins not only helps modulate pain but also has anti-inflammatory and immune-regulating effects. LDN is believed to reduce the activation of microglial cells, which are key players in neuroinflammation and central sensitization, both of which contribute to chronic pain and autoimmune conditions. Additionally, LDN impacts the production of pro-inflammatory cytokines, reducing the levels of molecules like IL-6 and TNF-alpha, thereby promoting immune balance and reducing systemic inflammation. Through these combined actions, LDN helps modulate pain, reduce inflammation, and restore immune function.
High-dose naltrexone works by acting as a full opioid receptor antagonist, meaning it binds to opioid receptors, primarily the mu-opioid receptor, without activating them. This blocks the effects of opioids like morphine, heroin, and endogenous opioids, preventing the euphoric or analgesic effects associated with opioid use. In conditions of opioid addiction or overdose, high-dose naltrexone helps by reducing cravings and preventing the reinforcing effects of opioids, thereby assisting in relapse prevention. Unlike low-dose naltrexone, high-dose naltrexone doesn’t stimulate the production of endogenous opioids but instead fully blocks receptor activation to maintain opioid abstinence. Additionally, it can block the effects of alcohol by interfering with its reward pathways in the brain, making it useful in alcohol dependence treatment.
Low-dose naltrexone (LDN) reduces inflammation by modulating the body’s immune system. It blocks opioid receptors for a short period, leading to increased production of endorphins, which helps regulate immune responses and lower inflammatory markers like pro-inflammatory cytokines. This anti-inflammatory effect makes LDN beneficial in treating chronic inflammatory disorders such as multiple sclerosis, fibromyalgia, and Crohn’s disease.
Low-dose naltrexone (LDN) combats oxidative stress by modulating immune function and promoting the release of endogenous opioids, which have antioxidant properties. This process helps neutralize free radicals, reducing oxidative damage to tissues. By minimizing oxidative stress, LDN may protect against chronic conditions linked to inflammation and oxidative damage.
Low-dose naltrexone (LDN) modulates the immune system by regulating the production of pro-inflammatory cytokines and enhancing immune balance. LDN temporarily blocks opioid receptors, which triggers the body to release endogenous opioids, helping to modulate immune cell activity. This modulation reduces inflammation and promotes immune homeostasis, making LDN beneficial in treating autoimmune and immune-mediated conditions.
Low-dose naltrexone (LDN) shows potential in cancer therapy by modulating the immune system and promoting apoptosis in cancer cells. It can upregulate the body’s natural immune response to target cancer cells, reduce tumor progression, and enhance the effects of traditional cancer treatments like chemotherapy. LDN’s ability to modulate macrophage activity and suppress oncogenic pathways, such as the PI3K/AKT/mTOR pathway, makes it a promising adjunctive treatment in various cancers.
Low-dose naltrexone (LDN) has shown potential in treating autoimmune conditions by modulating the immune system. LDN works by briefly blocking opioid receptors, which leads to increased endorphin production, subsequently regulating immune responses. This action helps reduce inflammation and autoimmune activity, making it a promising therapy for conditions such as multiple sclerosis, psoriasis, and other immune-mediated disorders.
Low-dose naltrexone (LDN) has been found to reduce insulin resistance by addressing inflammation, which plays a critical role in metabolic disorders. LDN modulates the immune system and reduces pro-inflammatory cytokines, which can improve insulin sensitivity and reduce the risk of diabetes and other metabolic conditions.
Low-dose naltrexone (LDN) has been increasingly studied for its potential benefits in improving skin health. By modulating the immune system and reducing inflammation, LDN may help alleviate various dermatological conditions, including chronic skin disorders like eczema, psoriasis, and Hailey-Hailey disease. LDN’s ability to reduce inflammation and modulate immune responses contributes to better skin barrier function and healing.
Low-dose naltrexone (LDN) has been shown to alleviate chronic pain by modulating the body’s immune and inflammatory responses. By temporarily blocking opioid receptors, LDN triggers a compensatory increase in the production of endorphins and other endogenous opioids, which helps reduce pain perception. Additionally, LDN decreases inflammation by reducing pro-inflammatory cytokines, making it a promising option for managing chronic pain conditions like fibromyalgia, neuropathy, and corneal pain.
High-dose naltrexone, especially in combination with bupropion, has shown promise in promoting weight loss through mechanisms involving appetite suppression and the modulation of reward pathways in the brain. This combination acts on the hypothalamus and mesolimbic dopamine pathways to reduce food cravings and increase feelings of satiety, helping patients manage their weight more effectively. Naltrexone also blocks the opioid receptors that can enhance the pleasurable effects of food, reducing overeating and binge behaviors.
Naltrexone, primarily used for alcohol and opioid dependence, has been explored for its efficacy in helping smokers quit by reducing cravings and withdrawal symptoms. By blocking opioid receptors, naltrexone reduces the rewarding effects of nicotine, making smoking less pleasurable and reducing urges. Studies suggest that naltrexone, either alone or in combination with other therapies like bupropion or nicotine replacement, may support smoking cessation, particularly in heavy drinkers and individuals with co-occurring substance use disorders.
Naltrexone has shown potential in treating impulse control disorders by modulating the brain’s reward system, which is often implicated in compulsive behaviors. It works by blocking opioid receptors, which play a role in the release of dopamine, a neurotransmitter associated with reward and pleasure. By inhibiting these pathways, naltrexone can reduce the compulsive urges and behaviors seen in disorders like pathological gambling and substance abuse.
Naltrexone, particularly in low doses, has shown effectiveness in managing chronic pain through its unique mechanism of modulating the central nervous system’s opioid receptors. By temporarily blocking these receptors, naltrexone triggers an increase in endorphins and other neurotransmitters that help reduce pain perception and inflammation. This mechanism is especially beneficial in conditions like fibromyalgia, multiple sclerosis, and chronic pain syndromes, offering patients relief with a low risk of addiction or tolerance.
Naltrexone, an opioid antagonist, has been widely researched for its efficacy in treating alcohol dependence by reducing cravings and heavy drinking episodes. It works by blocking the rewarding effects of alcohol, helping to reduce the urge to drink.
Naltrexone, especially in its extended-release form, has been found to be an effective pharmacological treatment for opioid addiction by blocking opioid receptors, reducing cravings, and preventing the euphoric effects of opioids. Its use is beneficial for individuals aiming to maintain long-term abstinence from opioids, particularly in countries where other opioid-replacement therapies like methadone and buprenorphine are not available.
Naltrexone side effects are very uncommon. There have been some side effects associated with the use of this drug wherein the patient had one of the issues listed below at some point while being on naltrexone. However, these side effects weren’t confirmed to be associated with the treatment and could have been a coincidence and not related to the use of naltrexone. Despite this, it was listed as a side effect associated with naltrexone even though these associated side effects are very uncommon.
Side effects associated with naltrexone may include the following:
Naltrexone is widely used in the treatment of alcohol and opioid addiction. It works by blocking the receptors in the brain that respond to these substances, thereby reducing cravings and preventing the euphoric effects that typically reinforce addiction. This makes Naltrexone a key component in many addiction recovery programs, especially for individuals who have already undergone detoxification.
Beyond addiction treatment, naltrexone is also used at lower doses for off-label applications, such as managing chronic pain and autoimmune disorders. In low-dose form (Low-Dose Naltrexone or LDN), it is believed to modulate the immune system and reduce inflammation, offering relief for conditions like fibromyalgia, multiple sclerosis, and Crohn’s disease. Although research is still ongoing, many patients report significant benefits from LDN therapy.
Naltrexone is available in both oral and extended-release injectable forms, allowing for flexible treatment options. The oral form is typically taken daily, while the injectable version, which lasts for about a month, is often chosen for patients who struggle with medication adherence. By offering multiple uses and formulations, Naltrexone has become a versatile tool in managing both addiction and various chronic conditions.
Naltrexone belongs to the drug class known as opioid antagonists. These drugs work by blocking the opioid receptors in the brain, preventing the euphoric and sedative effects of opioids. This makes Naltrexone particularly effective in treating opioid addiction, as it reduces cravings and eliminates the reinforcing effects of opioid use.
In addition to its role in opioid addiction, Naltrexone is also used to manage alcohol dependence. By modulating the brain’s reward system, Naltrexone decreases the pleasure derived from alcohol consumption, helping individuals maintain sobriety. Its versatility in treating both alcohol and opioid use disorders highlights its importance within the opioid antagonist drug class.
Low-Dose Naltrexone (LDN) is an off-label use that falls outside traditional addiction treatment. In lower doses, Naltrexone is used for its anti-inflammatory and immune-modulating properties, offering benefits for patients with chronic pain and autoimmune diseases. This expanded application shows how the drug’s classification extends beyond addiction management to address broader health conditions.
Naltrexone dosage varies depending on the condition being treated and the formulation used. For alcohol or opioid addiction, the standard oral dosage is typically 50 mg per day. Alternatively, an extended-release injectable form, administered as a 380 mg dose once every four weeks, is often prescribed for individuals who struggle with daily adherence to oral medication.
In some cases, Naltrexone is prescribed in much lower doses, known as Low-Dose Naltrexone (LDN), ranging from 1.5 mg to 4.5 mg per day. LDN is used off-label for managing chronic pain, autoimmune conditions, and certain inflammatory diseases. The low-dose regimen leverages the drug’s anti-inflammatory and immune-modulating effects, offering potential benefits beyond its traditional use in addiction treatment.
Before initiating treatment, it is crucial for individuals to be opioid-free for at least 7-10 days to avoid precipitated withdrawal. Dosage adjustments and careful monitoring by a healthcare provider are necessary to ensure safety and effectiveness, particularly in patients with liver or kidney conditions, as Naltrexone can impact liver function at higher doses.
Naltrexone has gained attention as a potential aid for weight loss, particularly when combined with other medications like bupropion in formulations such as Contrave. The drug works by modulating the brain’s reward pathways and reducing food cravings, particularly for high-calorie, highly palatable foods. By influencing these pathways, Naltrexone may help people better control their appetite and reduce emotional or binge eating.
In low doses, often referred to as Low-Dose Naltrexone (LDN), the medication is also believed to have an impact on metabolic function and inflammation, which are key factors in weight management. Some research suggests that LDN can help regulate insulin sensitivity, reduce chronic inflammation, and support a healthier metabolism, all of which contribute to improved weight loss outcomes.
However, while some studies and anecdotal reports show promising results, more extensive clinical trials are needed to confirm Naltrexone’s effectiveness and safety specifically for weight loss. As with any weight loss medication, it should be used under the guidance of a healthcare provider, alongside a balanced diet and regular exercise, to achieve the best long-term results.
Naltrexone, primarily known for its role in treating alcohol and opioid addiction, has garnered attention for its off-label uses in recent years. One notable off-label application is its use in managing chronic pain and inflammation. Low-Dose Naltrexone (LDN) has been found to potentially reduce symptoms associated with conditions such as fibromyalgia and multiple sclerosis by modulating the immune system and decreasing inflammation.
In addition to pain management, LDN is being explored for its potential benefits in treating autoimmune disorders. Research suggests that it may help modulate the immune response in conditions like Crohn’s disease and rheumatoid arthritis, offering a complementary approach to traditional treatments. The mechanism behind this effect is believed to involve the regulation of immune system activity and reduction of inflammatory responses.
Despite the promising results from various studies, more research is needed to fully understand the efficacy and safety of naltrexone for these off-label uses. Its application outside of addiction treatment remains an area of active investigation, and patients should consult with healthcare providers to weigh the potential benefits and risks based on their individual health needs.
The Sinclair Method is a treatment approach for alcohol addiction that involves using Naltrexone as a key component. This method, developed by Dr. John Sinclair, leverages Naltrexone’s ability to block opioid receptors in the brain, which are associated with the pleasure and reward system of drinking alcohol. By taking Naltrexone before drinking, the method aims to reduce the positive reinforcement of alcohol consumption, gradually diminishing the urge to drink over time.
The Sinclair Method is unique because it integrates Naltrexone into a gradual reduction strategy. Instead of aiming for immediate abstinence, the method encourages individuals to continue drinking, but with Naltrexone reducing the pleasurable effects of alcohol. This approach helps in retraining the brain’s reward pathways, allowing individuals to develop a new relationship with alcohol and reduce their dependence more sustainably.
Research on the Sinclair Method suggests that it can be highly effective for many individuals struggling with alcohol addiction. Studies have shown that the method can lead to significant reductions in drinking behavior and alcohol cravings. However, success with the Sinclair Method requires adherence to the prescribed Naltrexone regimen and a commitment to following the treatment plan, emphasizing that it is most effective when combined with behavioral support and counseling.
Naltrexone is an opioid antagonist that blocks the effects of opioids by binding to opioid receptors without activating them. This helps to reduce cravings and prevent relapse in individuals who have already detoxified from opioids. It can also be used in the treatment of alcohol dependence and has a non-addictive profile, making it a suitable option for long-term management.
Suboxone, on the other hand, is a combination of buprenorphine and naloxone. Buprenorphine is a partial opioid agonist, meaning it activates opioid receptors but to a lesser extent than full agonists like heroin or prescription opioids. This helps to alleviate withdrawal symptoms and cravings without producing the intense high associated with opioid use. Naloxone is included to prevent misuse by causing withdrawal symptoms if the medication is injected. Suboxone is often used during the initial stages of opioid recovery and can be effective for long-term maintenance therapy.
Choosing between Naltrexone and Suboxone depends on various factors, including the patient’s current state of opioid use, treatment goals, and individual health conditions. Naltrexone is typically used after a period of opioid detoxification, while Suboxone is often employed during the early stages of recovery to manage withdrawal symptoms and cravings. Both medications play important roles in addiction treatment, and their use should be tailored to each individual’s needs and circumstances.
Naltrexone injection is a long-acting formulation used primarily to support the treatment of alcohol and opioid dependence. Administered as an intramuscular injection, it offers a convenient alternative to daily oral naltrexone, providing continuous therapeutic levels of the medication. This method of administration ensures consistent medication levels in the bloodstream, which can enhance adherence and efficacy for individuals struggling with addiction.
The injection is typically administered once a month, making it a practical choice for those who prefer less frequent dosing compared to daily oral tablets. This long-acting approach can be particularly beneficial for individuals who have difficulty adhering to a daily medication regimen. It also helps reduce the risk of relapse by maintaining a steady blockade against the euphoric effects of alcohol and opioids, which can support sustained recovery.
One key advantage of the naltrexone injection is its ability to provide a consistent therapeutic effect without the fluctuations that can occur with daily oral dosing. However, it’s important for patients to be committed to abstinence from alcohol or opioids before starting the injection, as using the medication while still consuming these substances can lead to severe withdrawal symptoms. Regular follow-ups with a healthcare provider are essential to monitor the injection’s effectiveness and manage any potential side effects.
Naltrexone treatment for opioid withdrawal symptoms involves the use of this medication to manage and reduce cravings for opioids. By blocking opioid receptors in the brain, Naltrexone effectively prevents the euphoric effects of opioids, which can help individuals remain abstinent. This approach supports recovery by diminishing the psychological and physical drive to use opioids, thus aiding in the transition away from dependence.
During the initial phase of opioid withdrawal, patients may experience a range of symptoms including anxiety, muscle aches, and gastrointestinal distress. Naltrexone, however, is generally not recommended for use until after the patient has completed the detoxification process, as taking it too early can precipitate withdrawal symptoms or exacerbate discomfort. Once detoxified, patients can start Naltrexone therapy to maintain abstinence and support long-term recovery efforts.
In addition to its role in preventing relapse, Naltrexone can be an important component of a comprehensive treatment plan for opioid dependence. It is often used in conjunction with counseling, behavioral therapies, and support groups to address the multifaceted nature of addiction. Overall, Naltrexone provides a valuable tool for managing opioid withdrawal and supporting sustained recovery, helping individuals regain control of their lives and work towards a healthier future.
Naltrexone is used to manage opioid use disorder and alcohol dependence by blocking the effects of opioids and reducing cravings. It prevents the euphoric effects of these substances, supporting abstinence and recovery in individuals with opioid use disorder. By mitigating cravings and blocking opioid effects, naltrexone aids in the overall treatment strategy for opioid use disorder.
Naltrexone, often combined with bupropion in the medication Contrave, can aid weight loss by altering the brain’s reward system, reducing appetite, and decreasing cravings for food. This mechanism is particularly relevant in the context of opioid use disorder, as naltrexone is also used to manage this condition by blocking opioid receptors and reducing cravings for opioids. Additionally, naltrexone’s impact on the brain’s reward pathways can provide benefits for individuals dealing with opioid use disorder, supporting their recovery efforts and promoting overall well-being.
Naltrexone hydrochloride is not typically used to treat anxiety. However, its role in modulating neurotransmitter systems may have indirect effects on mood and anxiety, though this is not its primary use. Naltrexone hydrochloride primarily focuses on managing addiction and supporting recovery, rather than addressing anxiety directly
Naltrexone blocks the pleasurable effects of opioids and, to a lesser extent, may reduce the pleasure associated with other addictive substances. It is used to treat alcohol dependence by preventing the euphoric effects of alcohol and reducing cravings. While it does not block all pleasure or affect the pleasure derived from non-addictive activities, its primary role in treating alcohol dependence help support recovery and prevent relapse.
Naltrexone blocks opioid receptors in the brain, preventing the effects of opioids. The use of extended-release injectable naltrexone can provide a long-lasting block of opioid effects, which supports treatment for addiction. It can also affect neurotransmitter systems involved in reward and craving, further aiding recovery.
While taking naltrexone, avoid using opioids, as the drug will block their effects and could lead to withdrawal symptoms. It’s also important to follow medical advice regarding alcohol and other substances.
Feeling unusual on naltrexone could be due to side effects such as nausea, dizziness, or fatigue, especially if the medication is being used to manage cravings for illicit drugs. If these symptoms persist or are severe, consult a healthcare provider to ensure that naltrexone is effectively addressing issues related to illicit drugs without causing undue discomfort. Additionally, if you experience any unexpected reactions, it is important to discuss them with your healthcare provider, as they can help manage side effects while addressing issues related to illicit drugs.
Besides treating addiction, naltrexone is used off-label for chronic pain conditions, autoimmune disorders, and certain types of cancer. It is also explored for potential benefits in treating alcohol use disorder, among other conditions. Additionally, naltrexone’s role in managing alcohol use disorder is being investigated, highlighting its potential in supporting various therapeutic areas.
Naltrexone may offer benefits such as reducing symptoms of chronic pain, improving conditions like fibromyalgia, and potentially supporting immune system function. Additionally, naltrexone is effective in treating alcohol use disorder, helping to reduce cravings and support abstinence. Its use in low doses has shown promise for these applications, including managing alcohol use disorder.
The benefits of taking naltrexone include reduced cravings for alcohol and opioids, decreased risk of relapse, and support for sustained recovery, which align with goals set by the Mental Health Services Administration. It also may provide benefits in managing certain chronic pain and autoimmune conditions, contributing to overall well-being as supported by guidelines from the Mental Health Services Administration. Additionally, naltrexone’s role in addiction treatment and chronic disease management reflects the broader objectives of the Mental Health Services Administration to enhance patient care and recovery outcomes.
Naltrexone, when used in combination with bupropion (as Contrave), can aid weight loss by reducing hunger and cravings through its effects on the brain’s reward system. Starting naltrexone in this combination can help manage appetite and support weight management goals. It’s important to consult with a healthcare provider when starting naltrexone to ensure it is appropriate for your weight loss plan. Additionally, starting naltrexone should be done under medical supervision to monitor for potential side effects and adjust the treatment as needed.
People are prescribed naltrexone to help manage opioid or alcohol dependence by blocking opioid receptors, including the kappa opioid receptors, which can reduce cravings and prevent relapse. It is also used for certain off-label conditions, such as chronic pain and autoimmune diseases, by influencing various opioid receptor types, including kappa opioid receptors. By targeting these receptors, naltrexone helps in the broader management of these conditions.
The most common side effects of naltrexone include nausea, headache, dizziness, fatigue, and insomnia. In rare cases, naltrexone may lead to more serious conditions such as acute hepatitis, which requires immediate medical attention. These side effects, including potential acute hepatitis, are generally mild and tend to improve over time.
Naltrexone works by blocking opioid receptors in the brain, which prevents opioids from binding and producing their effects. This action reduces the reward and reinforcement associated with opioid and alcohol use. The effectiveness of naltrexone is closely tied to the naltrexone dose used, as different doses can impact the level of receptor blockade and therapeutic outcomes. Adjusting the naltrexone dose may be necessary to optimize treatment for individual needs and manage side effects.
Naltrexone is an opioid antagonist, meaning it blocks the effects of opioids at receptor sites in the brain. This medication is approved by the Food and Drug Administration (FDA) for managing opioid and alcohol dependence. The Food and Drug Administration has also recognized naltrexone’s role in supporting addiction recovery by reducing cravings and preventing relapse.
Naltrexone is classified as an opioid antagonist and is commonly used to treat alcohol dependence. As an opioid antagonist, it blocks the effects of opioids and can also help to treat alcohol cravings by reducing the pleasure associated with drinking. Its role in treating alcohol dependence makes it a valuable tool in comprehensive addiction treatment plans.
No, naltrexone is not a scheduled narcotic. It is not classified as a controlled substance due to its non-addictive nature, unlike other drugs that are tightly regulated. Naltrexone’s status as a non-controlled substance means it is generally considered safer and has fewer restrictions compared to other drugs with potential for abuse.
Naloxone and naltrexone are both opioid antagonists. They block opioid receptors but are used in different contexts; naloxone is primarily for reversing opioid overdoses, while naltrexone is used for long-term management of opioid and alcohol dependence. Unlike other drugs that may activate opioid receptors, naltrexone prevents opioids from producing their effects, supporting addiction treatment. Naloxone, on the other hand, is utilized in emergency situations to counteract the effects of opioid overdoses, which can be a critical intervention compared to other drugs used in overdose scenarios. Both medications offer important functions, with naltrexone helping to manage addiction in the long term and naloxone providing immediate reversal of overdose effects.
Yes, naltrexone can contribute to weight loss, especially when combined with bupropion as part of the medication Contrave. It helps reduce appetite and cravings, which can be particularly beneficial for those dealing with issues related to drug abuse. By supporting weight management, naltrexone also aids in addressing the behavioral patterns associated with drug abuse. The intramuscular injection of naltrexone, administered as VIVITROL, provides a long-lasting effect that supports sustained weight management. This method of delivery ensures consistent therapeutic levels of the medication, enhancing its benefits for weight control.
Naltrexone and Wellbutrin (bupropion) cause weight loss by targeting different pathways in the brain that influence appetite and cravings. Naltrexone, typically administered at a dose of 50 mg, reduces hunger and cravings, including those for other opioids, while bupropion may increase metabolism and decrease appetite. This combination of 50 mg naltrexone and bupropion helps manage cravings not only for food but also for other opioids, supporting more comprehensive weight management.
The effectiveness of weight loss medications varies by individual, but options like semaglutide (Wegovy) and liraglutide (Saxenda) are among the strongest and most effective prescription weight loss treatments currently available. Additionally, understanding the impact of various medications on opioid receptors can be informed by the naloxone challenge test, which often uses a dose of 50 mg of naloxone. This test helps assess the response to opioid antagonists and can provide insights into how weight loss medications might interact with the opioid system. The naloxone challenge test, with a typical dosage of 50 mg, can be particularly useful in evaluating the effectiveness of treatments in individuals with complex medical profiles, and a similar dosage of 50 mg is used to ensure accurate and reliable results.
The action of naltrexone involves blocking opioid receptors in the brain, which prevents the effects of opioid drugs and reduces cravings for substances like alcohol and opioids. When prescribing naltrexone, healthcare providers should advise patients to undergo regular liver function tests, as the drug can impact liver health. Monitoring liver function tests ensures that any potential liver issues are detected early, helping to maintain overall health during treatment. Additionally, providers should advise patients on the importance of adhering to this monitoring regimen. Regular testing helps in managing any side effects and ensures the effectiveness of the treatment plan.
Both naloxone and naltrexone act as opioid antagonists. They bind to opioid receptors without activating them, thus blocking the effects of opioid drugs. Naloxone is used for emergency opioid overdose reversal, while naltrexone, typically administered at a dosage of 50 mg, is used for long-term management of addiction and in substance abuse treatment. Naltrexone’s role in substance abuse treatment includes reducing cravings and supporting recovery by preventing the euphoric effects of opioids. For some treatment protocols, such as the Sinclair Method, 50 mg of naltrexone is used to help decrease alcohol consumption by reducing cravings.
Naltrexone is not specifically a dopamine blocker. It primarily blocks opioid receptors, which are associated with opioid medications, and indirectly affects the dopaminergic system involved in the reward and pleasure pathways. By blocking the effects of opioid medications, naltrexone, typically administered at 50 mg, helps in managing addiction and reducing cravings. The 50 mg dose of naltrexone is effective in diminishing the rewarding effects of opioids and supporting recovery efforts.
While naltrexone alone has shown some effects on weight loss, a common dosage is 50 mg, and it is often used in combination with bupropion (as Contrave) for more significant and effective weight management. Unlike opioid agonists, which activate opioid receptors, naltrexone at 50 mg blocks these receptors to reduce cravings and appetite. This combination approach provides a more comprehensive strategy for weight management, contrasting with the effects of opioid agonists that can influence the reward system in a different manner.
New uses for naltrexone include its application in treating autoimmune disorders, chronic pain conditions, and certain cancers. For some of these conditions, naltrexone is administered at a dose of 50 mg. By blocking the mu opioid receptor, 50 mg of naltrexone may offer potential benefits in these areas, though its exact mechanisms are still being studied. Its effects on the mu opioid receptor and its implications for treatment at this dose are actively being explored to understand its full range of applications.
Yes, naltrexone is used for various conditions beyond addiction treatment, including chronic joint and muscle pain management, autoimmune disorders, and certain off-label uses like cancer treatment. Its potential benefits extend to alleviating joint and muscle pain, making it a versatile option in pain management. Additionally, naltrexone’s use in managing joint and muscle pain demonstrates its broader therapeutic applications beyond its primary indications.
Off-label uses of naloxone include its application in treating severe itching associated with some medical conditions and for potential use in certain substance abuse treatments, though its primary use remains for opioid overdose reversal by targeting opiate receptors. Naloxone works by binding to opiate receptors in the brain, thereby displacing opioids and reversing their effects. This mechanism is crucial for effectively addressing opioid overdoses and mitigating their impact on the body.
The Sinclair Method typically involves taking 50 mg of naltrexone about an hour before drinking alcohol. This regimen aims to reduce alcohol cravings and support moderation. It is important to note that a positive urine screen for alcohol consumption might still occur, even with adherence to the Sinclair Method. The goal of the method is to gradually decrease the frequency of positive urine screens by diminishing the desire for alcohol over time.
The Sinclair Method has been shown to be effective for many individuals in reducing alcohol consumption and supporting recovery by decreasing the desire for alcohol through the use of naltrexone. This approach can also be relevant for those struggling with opioid addiction, as naltrexone can help manage opioid intoxication by blocking the effects of opioids. By reducing the craving and reinforcing the behavior change, the Sinclair Method supports long-term recovery from both alcohol and opioid intoxication.
Side effects of the Sinclair Method can include nausea, dizziness, headache, and fatigue. These side effects are generally mild but can affect adherence to the treatment. Missing a dose or experiencing a missed dose can also impact the effectiveness of the treatment and lead to increased cravings or relapse. It’s important to address any missed doses promptly to maintain the intended benefits of the Sinclair Method.
No, naltrexone is not the same as Suboxone. Naltrexone is an opioid antagonist used to manage addiction, and if a missed dose occurs, it can affect the effectiveness of the treatment. Suboxone, on the other hand, is a combination of buprenorphine (a partial opioid agonist) and naloxone (an opioid antagonist), used to treat opioid dependence. Missing a dose of either medication can impact treatment outcomes, so it’s important to adhere to the prescribed schedule to maintain effectiveness.
Naloxone is an opioid antagonist used to reverse opioid overdoses, while Suboxone combines buprenorphine (which partially activates opioid receptors) with naloxone (which blocks opioid effects) to treat opioid dependence and reduce misuse. Both naloxone and Suboxone are associated with potential adverse events, though these are generally manageable. Monitoring for adverse events is crucial during treatment to ensure safety and efficacy.
The equivalent of naltrexone in terms of its action is naloxone, as both are opioid antagonists. However, naloxone is primarily used for emergency overdose situations, while naltrexone, particularly at a lower dose, is used for long-term management of addiction. A lower dose of naltrexone can also be effective for certain off-label uses.
A VIVITROL shot delivers naltrexone in an extended-release form, which helps prevent relapse by blocking the effects of opioids and reducing cravings for alcohol. It is used as part of a complete treatment program for addiction. By integrating VIVITROL with other therapeutic interventions, individuals can benefit from a complete treatment program that addresses both the physiological and psychological aspects of addiction. This approach ensures a more robust and effective strategy for long-term recovery as part of a complete treatment program.
Yes, VIVITROL is a brand name for the extended-release injectable form of naltrexone. It provides long-lasting effects for managing opioid and alcohol dependence and is used to treat alcohol use disorders. By blocking the effects of alcohol and opioids, VIVITROL helps to treat alcohol use and prevent relapse.
Naltrexone injections, such as VIVITROL, are typically administered into the gluteal muscle (buttocks) by a healthcare professional, as supported by clinical studies. This method of administration ensures proper absorption and effectiveness of the medication, a fact demonstrated in numerous clinical studies. The administration process is designed to maximize the benefits of naltrexone, as confirmed by clinical studies on its efficacy and safety.
Naloxone injection is used to rapidly reverse opioid overdoses by restoring normal breathing and consciousness in individuals who have overdosed on opioids. While naloxone is specifically for opioid overdoses, addressing alcohol abuse often requires different approaches. For those struggling with alcohol abuse, medications and therapies targeting alcohol use disorder are used to support recovery and reduce the risk of relapse. Naloxone is crucial in the context of opioid emergencies, but comprehensive treatment plans for alcohol abuse involve a variety of interventions tailored to individual needs.
Patten DK, Schultz BG, Berlau DJ. The Safety and Efficacy of Low-Dose Naltrexone in the Management of Chronic Pain and Inflammation in Multiple Sclerosis, Fibromyalgia, Crohn’s Disease, and Other Chronic Pain Disorders. Pharmacotherapy. 2018 Mar;38(3):382-389. doi: 10.1002/phar.2086. Epub 2018 Feb 23. PMID: 29377216.
The Safety and Efficacy of Low-Dose Naltrexone in the Management of Chronic Pain and Inflammation in Multiple Sclerosis, Fibromyalgia, Crohn’s Disease, and Other Chronic Pain Disorders
Low-dose naltrexone (LDN) has been used off-label for chronic pain and inflammatory conditions like multiple sclerosis, fibromyalgia, and Crohn’s disease due to its potential anti-inflammatory and analgesic effects. While evidence supports its safety and tolerability, studies on its efficacy are limited, often focusing on subjective outcomes like quality of life or self-reported pain. More randomized controlled trials are needed to confirm its effectiveness.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/29377216/.
Younger J, Parkitny L, McLain D. The use of low-dose naltrexone (LDN) as a novel anti-inflammatory treatment for chronic pain. Clin Rheumatol. 2014 Apr;33(4):451-9. doi: 10.1007/s10067-014-2517-2. Epub 2014 Feb 15. PMID: 24526250; PMCID: PMC3962576.
The use of low-dose naltrexone (LDN) as a novel anti-inflammatory treatment for chronic pain
Low-dose naltrexone (LDN) shows promise in treating chronic conditions like fibromyalgia and multiple sclerosis by modulating central nervous system inflammation, particularly through microglial cells, rather than its traditional opioid receptor activity. While inexpensive and well-tolerated, its use remains experimental due to limited and small-scale clinical trials.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/24526250/.
Choubey A, Girdhar K, Kar AK, Kushwaha S, Yadav MK, Ghosh D, Mondal P. Low-dose naltrexone rescues inflammation and insulin resistance associated with hyperinsulinemia. J Biol Chem. 2020 Nov 27;295(48):16359-16369. doi: 10.1074/jbc.RA120.013484. Epub 2020 Sep 17. PMID: 32943552; PMCID: PMC7705311.
Low-dose naltrexone rescues inflammation and insulin resistance associated with hyperinsulinemia
Hyperinsulinemia promotes systemic insulin resistance by inducing inflammation through the repression of SIRT1 and activation of NF-κB in macrophages. Low-dose naltrexone (LDN) counteracts this process by restoring SIRT1 activity and reducing inflammation, improving insulin sensitivity in hyperinsulinemic conditions. This suggests LDN may be a potential therapy for insulin resistance linked to hyperinsulinemia.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/32943552/.
Lie MRKL, van der Giessen J, Fuhler GM, de Lima A, Peppelenbosch MP, van der Ent C, van der Woude CJ. Low dose Naltrexone for induction of remission in inflammatory bowel disease patients. J Transl Med. 2018 Mar 9;16(1):55. doi: 10.1186/s12967-018-1427-5. PMID: 29523156; PMCID: PMC5845217.
Low dose Naltrexone for induction of remission in inflammatory bowel disease patients
Low-dose Naltrexone (LDN) shows promise as a safe alternative treatment for inflammatory bowel disease (IBD) patients who are unresponsive to conventional therapies. In a 12-week study, 74.5% of patients experienced clinical improvement, with 25.5% achieving remission. LDN was found to enhance wound healing and reduce endoplasmic reticulum stress in intestinal epithelial cells, though it did not significantly affect cytokine levels. These findings suggest LDN may effectively improve epithelial barrier function and offer a novel therapeutic option for refractory IBD cases.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/29523156/.
Parkitny L, Younger J. Reduced Pro-Inflammatory Cytokines after Eight Weeks of Low-Dose Naltrexone for Fibromyalgia. Biomedicines. 2017 Apr 18;5(2):16. doi: 10.3390/biomedicines5020016. PMID: 28536359; PMCID: PMC5489802.
Reduced Pro-Inflammatory Cytokines after Eight Weeks of Low-Dose Naltrexone for Fibromyalgia
This 10-week trial tested the effects of low-dose naltrexone (LDN) on fibromyalgia, involving eight women. LDN treatment was linked to reduced levels of various pro-inflammatory cytokines and resulted in a 15% pain reduction and an 18% decrease in overall symptoms, suggesting its potential as an anti-inflammatory treatment for fibromyalgia.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/28536359/.
Partridge S, Quadt L, Bolton M, Eccles J, Thompson C, Colasanti A, Bremner S, Jones CI, Bruun KD, Van Marwijk H. A systematic literature review on the clinical efficacy of low dose naltrexone and its effect on putative pathophysiological mechanisms among patients diagnosed with fibromyalgia. Heliyon. 2023 Apr 19;9(5):e15638. doi: 10.1016/j.heliyon.2023.e15638. PMID: 37206027; PMCID: PMC10189400.
A systematic literature review on the clinical efficacy of low dose naltrexone and its effect on putative pathophysiological mechanisms among patients diagnosed with fibromyalgia
This study reviewed the limited evidence supporting low-dose naltrexone (LDN) for fibromyalgia pain management, finding some indication that LDN may reduce pain and improve quality of life. Two small studies suggest LDN’s effects might involve inflammatory markers, but the evidence is weak, biased, and based on female-only samples. More research, including in men and diverse populations, is needed.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/37206027/.
Younger J, Mackey S. Fibromyalgia symptoms are reduced by low-dose naltrexone: a pilot study. Pain Med. 2009 May-Jun;10(4):663-72. doi: 10.1111/j.1526-4637.2009.00613.x. Epub 2009 Apr 22. PMID: 19453963; PMCID: PMC2891387.
Fibromyalgia symptoms are reduced by low-dose naltrexone: a pilot study
This pilot clinical trial found that low-dose naltrexone significantly reduced fibromyalgia symptoms by over 30% compared to placebo, improving pain thresholds with minimal side effects. Participants with higher inflammation levels responded best to the treatment.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/19453963/.
Driver CN, D’Souza RS. Efficacy of Low-Dose Naltrexone and Predictors of Treatment Success or Discontinuation in Fibromyalgia and Other Chronic Pain Conditions: A Fourteen-Year, Enterprise-Wide Retrospective Analysis. Biomedicines. 2023 Apr 3;11(4):1087. doi: 10.3390/biomedicines11041087. PMID: 37189705; PMCID: PMC10135963.
Efficacy of Low-Dose Naltrexone and Predictors of Treatment Success or Discontinuation in Fibromyalgia and Other Chronic Pain Conditions: A Fourteen-Year, Enterprise-Wide Retrospective Analysis
Low-dose naltrexone (LDN) has shown potential as an analgesic for chronic pain conditions, particularly fibromyalgia, with 65% of patients reporting pain relief. Despite limited adverse effects, 36% discontinued use. Further research is needed to better understand its benefits.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/37189705/.
Li W, McIntyre RL, Schomakers BV, Kamble R, Luesink AHG, van Weeghel M, Houtkooper RH, Gao AW, Janssens GE. Low-dose naltrexone extends healthspan and lifespan in C. elegans via SKN-1 activation. iScience. 2024 May 8;27(6):109949. doi: 10.1016/j.isci.2024.109949. PMID: 38799567; PMCID: PMC11126937.
Low-dose naltrexone extends healthspan and lifespan in C. elegans via SKN-1 activation
This study explores the potential of low-dose naltrexone (LDN) as a geroprotector, showing that it extends healthspan and lifespan in C. elegans through SKN-1 signaling, which influences immune and oxidative stress responses, suggesting its promise for promoting healthy aging in humans.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/38799567/.
Agrawal YP. Low dose naltrexone therapy in multiple sclerosis. Med Hypotheses. 2005;64(4):721-4. doi: 10.1016/j.mehy.2004.09.024. PMID: 15694688.
Low dose naltrexone therapy in multiple sclerosis
Low-dose naltrexone is widely used by multiple sclerosis (MS) patients, with anecdotal evidence suggesting it prevents relapses and slows disease progression. It may work by reducing apoptosis in oligodendrocytes through decreasing nitric oxide synthase activity, which prevents glutamate neurotoxicity. Clinical trials are needed to validate its effectiveness.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/15694688/.
Berkson BM, Rubin DM, Berkson AJ. Revisiting the ALA/N (alpha-lipoic acid/low-dose naltrexone) protocol for people with metastatic and nonmetastatic pancreatic cancer: a report of 3 new cases. Integr Cancer Ther. 2009 Dec;8(4):416-22. doi: 10.1177/1534735409352082. Erratum in: Integr Cancer Ther. 2010 Jun;9(2):247. PMID: 20042414.
Revisiting the ALA/N (alpha-lipoic acid/low-dose naltrexone) protocol for people with metastatic and nonmetastatic pancreatic cancer: a report of 3 new cases
The authors report on the long-term survival of a man with pancreatic cancer treated with intravenous alpha-lipoic acid and oral low-dose naltrexone (ALA/N), noting he remains healthy 78 months later. They present three additional cases of pancreatic cancer patients treated with the same protocol, highlighting significant improvements: one patient is alive 39 months post-diagnosis, another showed no evidence of disease after five months, and a third had no signs of cancer after four months. The article discusses ALA’s multifaceted actions in reducing oxidative stress and enhancing apoptotic activity, alongside low-dose naltrexone’s role in modulating immune responses, advocating for clinical trials of the ALA/N protocol.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/20042414/.
Plank JR, Glover SC, Moloney BD, Hoeh NR, Sundram F, Sumner RL, Muthukumaraswamy S, Lin JC. A randomized, double-blind, placebo-controlled, hybrid parallel-arm study of low-dose naltrexone as an adjunctive anti-inflammatory treatment for major depressive disorder. Trials. 2022 Sep 30;23(1):822. doi: 10.1186/s13063-022-06738-3. PMID: 36175917; PMCID: PMC9524133.
A randomized, double-blind, placebo-controlled, hybrid parallel-arm study of low-dose naltrexone as an adjunctive anti-inflammatory treatment for major depressive disorder
This study investigates the potential of low-dose naltrexone (LDN) as an adjunctive treatment for major depressive disorder (MDD), particularly in patients with high inflammation, since current treatments are often ineffective. In a double-blind placebo-controlled trial involving 48 MDD patients, participants will be stratified based on inflammation levels and randomized to receive either LDN or a placebo for 12 weeks, followed by LDN for an additional 12 weeks. The trial aims to evaluate LDN’s antidepressant efficacy and explore the neurobiological and inflammatory mechanisms involved in MDD, potentially paving the way for better diagnostic tools and treatments for this condition.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/36175917/
Ciwun M, Tankiewicz-Kwedlo A, Pawlak D. Low-Dose Naltrexone as an Adjuvant in Combined Anticancer Therapy. Cancers (Basel). 2024 Mar 21;16(6):1240. doi: 10.3390/cancers16061240. PMID: 38539570; PMCID: PMC10968813.
Low-Dose Naltrexone as an Adjuvant in Combined Anticancer Therapy
Low-dose naltrexone (LDN), an opioid receptor antagonist primarily used for opioid and alcohol dependence, shows promise in cancer therapy by blocking the opioid growth factor receptor (OGFr), leading to increased opioid growth factor (OGF) synthesis, which inhibits cancer cell survival and proliferation. Studies indicate LDN’s potential as an effective adjuvant in chemotherapy and immunotherapy due to its unique mechanism, lack of direct cytotoxicity, and immunomodulating effects.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/38539570/.
Frech T, Novak K, Revelo MP, Murtaugh M, Markewitz B, Hatton N, Scholand MB, Frech E, Markewitz D, Sawitzke AD. Low-dose naltrexone for pruritus in systemic sclerosis. Int J Rheumatol. 2011;2011:804296. doi: 10.1155/2011/804296. Epub 2011 Sep 12. PMID: 21918649; PMCID: PMC3171757.
Low-dose naltrexone for pruritus in systemic sclerosis
Pruritus is a common yet poorly treated symptom of systemic sclerosis (SSc), an autoimmune disease affecting multiple organs. A case series involving three patients showed significant improvement in pruritus and gastrointestinal symptoms after using low-dose naltrexone (LDN), indicating it may be an effective and tolerable treatment option for these symptoms in SSc.
You can read the abstract of this article at
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3171757/.
Rupp A, Young E, Chadwick AL. Low-dose naltrexone’s utility for non-cancer centralized pain conditions: a scoping review. Pain Med. 2023 Nov 2;24(11):1270-1281. doi: 10.1093/pm/pnad074. PMID: 37302106; PMCID: PMC10628981.
Low-dose naltrexone’s utility for non-cancer centralized pain conditions: a scoping review.
Low-dose naltrexone (LDN) has been found to modulate inflammation by interrupting microglial activation in the central nervous system, suggesting its potential for managing pain from central sensitization. A scoping review identified 47 studies indicating that LDN may improve pain severity, hyperalgesia, physical function, quality of life, and sleep in patients with various chronic centralized pain conditions, although variability in dosing and response times was noted. The findings support further high-quality randomized control trials to better establish LDN’s efficacy and standardize treatment protocols.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/37302106/.
Bolton MJ, Chapman BP, Van M arwijk H. Low-dose naltrexone as a treatment for chronic fatigue syndrome. BMJ Case Rep. 2020 Jan 6;13(1):e232502. doi: 10.1136/bcr-2019-232502. PMID: 31911410; PMCID: PMC6954765.
Low-dose naltrexone as a treatment for chronic fatigue syndrome
Low-dose naltrexone (LDN) is used off-label to treat chronic immune-modulated disorders, showing promise in small trials for conditions like Crohn’s disease and fibromyalgia, but lacks clinical studies for chronic fatigue syndrome (CFS). A series of case reports from CFS patients indicate varied responses to LDN, ranging from significant improvements to partial symptom relief at doses between 4 and 12 mg. Further clinical trials are suggested to investigate LDN’s potential benefits for these chronic illnesses, which currently have no approved treatments.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/31911410/.
Brown N, Panksepp J. Low-dose naltrexone for disease prevention and quality of life. Med Hypotheses. 2009 Mar;72(3):333-7. doi: 10.1016/j.mehy.2008.06.048. Epub 2008 Nov 28. PMID: 19041189.
Low-dose naltrexone for disease prevention and quality of life. Med Hypotheses
Low-dose naltrexone (LDN) shows promise in treating various physical and mental disorders by modulating the immune system and enhancing endogenous opioid activity, potentially improving immune response, reducing inflammation, and promoting emotional well-being, stress resilience, and social bonding.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/19041189/.
de Carvalho JF, Skare T. Low-Dose Naltrexone in Rheumatological Diseases. Mediterr J Rheumatol. 2023 Mar 31;34(1):1-6. doi: 10.31138/mjr.34.1.1. PMID: 37223594; PMCID: PMC10201089.
Low-Dose Naltrexone in Rheumatological Diseases
Low-dose naltrexone (LDN), approved for alcohol and opioid abuse, shows promise as a safe treatment for various rheumatic diseases, including fibromyalgia, systemic sclerosis, dermatomyositis, Sjögren’s syndrome, and rheumatoid arthritis, with beneficial effects on pain and well-being, though more extensive studies are needed to confirm its efficacy.
You can read the abstract of this article at
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10201089/.
Kazemi R, Mohammadi M, Salimiyan S, Aliakbari S, Ahmadi M, Mohammad Reza R. Long-Term Effects of Low-Dose Naltrexone on Immunomodulatory Properties of Human Adipose-Derived Mesenchymal Stem Cells. Iran J Immunol. 2023 May 31;20(2):219-231. doi: 10.22034/iji.2023.95659.2385. Epub 2023 May 8. PMID: 37151015.
Long-Term Effects of Low-Dose Naltrexone on Immunomodulatory Properties of Human Adipose-Derived Mesenchymal Stem Cells
This study investigates the long-term effects of low-dose naltrexone (LDN) on human adipose-derived mesenchymal stem cells (ASCs) and their immunomodulatory properties. After 14 days of treatment, findings indicate that different LDN concentrations uniquely influence ASCs’ ability to modulate immune responses, with higher concentrations enhancing the expression of key immunomodulatory genes and cytokines in both unstimulated and stimulated ASCs.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/37151015/.
Yi Z, Guo S, Hu X, Wang X, Zhang X, Griffin N, Shan F. Functional modulation on macrophage by low dose naltrexone (LDN). Int Immunopharmacol. 2016 Oct;39:397-402. doi: 10.1016/j.intimp.2016.08.015. Epub 2016 Aug 23. PMID: 27561742.
Functional modulation on macrophage by low dose naltrexone (LDN)
Research indicates that low-dose naltrexone (LDN), primarily used for alcohol dependence and opioid addiction, significantly enhances macrophage function by increasing the expression of MHC II and CD64 while decreasing CD206. This treatment boosts the production of inflammatory cytokines TNF-α, IL-6, and IL-1β, and improves macrophage phagocytosis. These findings suggest LDN’s potential role in immune regulation, particularly in supporting CD4+ T cell interactions in AIDS treatment, as evidenced by its approval for such use in Nigeria.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/27561742/.
Pitt B, Tate AM, Gluck D, Rosenson RS, Goonewardena SN. Repurposing low-dose naltrexone for the prevention and treatment of immunothrombosis in COVID-19. Eur Heart J Cardiovasc Pharmacother. 2022 Jun 8;8(4):402-405. doi: 10.1093/ehjcvp/pvac014. PMID: 35179184; PMCID: PMC8903502.
Repurposing low-dose naltrexone for the prevention and treatment of immunothrombosis in COVID-19
COVID-19 is marked by significant immune dysregulation, characterized by hyperinflammation and thrombosis, which complicates treatment with traditional anticoagulants due to bleeding risks. This commentary suggests that low-dose naltrexone (LDN) could provide a novel therapeutic approach by modulating immune responses and reducing immune-mediated thrombotic complications associated with the disease.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/35179184/.
Kučić N, Rački V, Šverko R, Vidović T, Grahovac I, Mršić-Pelčić J. Immunometabolic Modulatory Role of Naltrexone in BV-2 Microglia Cells. Int J Mol Sci. 2021 Aug 5;22(16):8429. doi: 10.3390/ijms22168429. PMID: 34445130; PMCID: PMC8395119.
Immunometabolic Modulatory Role of Naltrexone in BV-2 Microglia Cells
Low-dose naltrexone (LDN) has been shown to shift microglial cells from a pro-inflammatory state to a quiescent anti-inflammatory state while promoting a metabolic switch from glycolysis to mitochondrial oxidative phosphorylation. In vitro studies using the BV-2 microglial cell line demonstrated that LDN effectively reprograms the immunometabolic profile of microglia, suggesting its potential as a novel treatment for neuroinflammatory conditions.
You can read the abstract of this article at
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8395119/.
Meng J, Meng Y, Plotnikoff NP, Youkilis G, Griffin N, Shan F. Low dose naltrexone (LDN) enhances maturation of bone marrow dendritic cells (BMDCs). Int Immunopharmacol. 2013 Dec;17(4):1084-9. doi: 10.1016/j.intimp.2013.10.012. PMID: 24455776.
Low dose naltrexone (LDN) enhances maturation of bone marrow dendritic cells (BMDCs)
The study investigates the effects of low-dose naltrexone (LDN) on bone marrow-derived dendritic cells (BMDCs), finding that LDN promotes their maturation by enhancing the expression of key molecules and cytokines while reducing phagocytosis and pinocytosis. The findings suggest LDN’s potential in immunoregulation, highlighting its application for boosting host immunity in cancer therapy and in developing dendritic cell-based vaccines for various diseases.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/24455776/.
Miskoff JA, Chaudhri M. Low Dose Naltrexone and Lung Cancer: A Case Report and Discussion. Cureus. 2018 Jul 5;10(7):e2924. doi: 10.7759/cureus.2924. PMID: 30197847; PMCID: PMC6126779.
Low Dose Naltrexone and Lung Cancer: A Case Report and Discussion. Cureus
Low dose naltrexone (LDN) shows potential as a complementary treatment for various medical disorders, particularly those involving the immune system, and has been linked to prolonged survival in a case of a 50-year-old male with prostate and lung cancer. While not a definitive cure, clinical trials suggest LDN may enhance immune responses against tumors, including non-small cell lung cancer (NSCLC).
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/30197847/.
Toljan K, Vrooman B. Low-Dose Naltrexone (LDN)-Review of Therapeutic Utilization. Med Sci (Basel). 2018 Sep 21;6(4):82. doi: 10.3390/medsci6040082. PMID: 30248938; PMCID: PMC6313374.
Low-Dose Naltrexone (LDN)-Review of Therapeutic Utilization
Naltrexone and naloxone, traditionally used as opioid antagonists, exhibit different effects at lower doses, with low-dose naltrexone (LDN) (1-5 mg) reducing glial inflammation and potentially benefiting conditions like fibromyalgia and multiple sclerosis. Ultra low-dose naltrexone/naloxone (ULDN), at doses under 1 μg, enhances opioid analgesia and minimizes postoperative opioid requirements, while very low-dose naltrexone (VLDN) (1 μg to 1 mg) is mainly an experimental adjunct for opioid tapering. However, research on these low-dose applications remains limited and requires further evaluation.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/30248938/.
Liu WM, Dalgleish AG. Naltrexone at low doses (LDN) and its relevance to cancer therapy. Expert Rev Anticancer Ther. 2022 Mar;22(3):269-274. doi: 10.1080/14737140.2022.2037426. Epub 2022 Feb 7. PMID: 35107043.
Naltrexone at low doses (LDN) and its relevance to cancer therapy
Naltrexone, originally designed to block opioid receptors, has shown potential benefits at lower doses for patients with chronic inflammatory and autoimmune conditions, and anecdotal evidence suggests it may also aid in cancer resolution. This review examines three mechanisms through which low-dose naltrexone (LDN) may influence cancer progression: antagonism of specific receptors, modulation of immune function, and inhibition of cancer cell signaling pathways. Given the increasing anecdotal reports of its efficacy, there is a growing interest in clinical trials for LDN as a complementary treatment in oncology, particularly alongside chemotherapy.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/35107043/.
Li Z, You Y, Griffin N, Feng J, Shan F. Low-dose naltrexone (LDN): A promising treatment in immune-related diseases and cancer therapy. Int Immunopharmacol. 2018 Aug;61:178-184. doi: 10.1016/j.intimp.2018.05.020. Epub 2018 Jun 7. PMID: 29885638.
Low-dose naltrexone (LDN): A promising treatment in immune-related diseases and cancer therapy
Naltrexone, primarily used for opioid addiction rehabilitation, has shown promising off-label uses, particularly as a low-dose naltrexone (LDN) immunomodulator in autoimmune diseases and certain cancers, alleviating symptoms of some mental disorders. Research indicates that LDN works by binding to opioid receptors on immune and tumor cells, highlighting its potential as a therapeutic agent in immunological and cancer treatments.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/29885638/.
Ma M, Wang X, Liu N, Shan F, Feng Y. Low-dose naltrexone inhibits colorectal cancer progression and promotes apoptosis by increasing M1-type macrophages and activating the Bax/Bcl-2/caspase-3/PARP pathway. Int Immunopharmacol. 2020 Jun;83:106388. doi: 10.1016/j.intimp.2020.106388. Epub 2020 Mar 11. PMID: 32171145.
Low-dose naltrexone inhibits colorectal cancer progression and promotes apoptosis by increasing M1-type macrophages and activating the Bax/Bcl-2/caspase-3/PARP pathway
This study investigates how low-dose naltrexone (LDN) inhibits colorectal cancer (CRC) progression by increasing M1-like macrophages and activating the Bax/Bcl-2/caspase-3/PARP signaling pathway, promoting tumor cell apoptosis, and suggests LDN’s potential as a CRC treatment.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/32171145/.
Liu WM, Scott KA, Dennis JL, Kaminska E, Levett AJ, Dalgleish AG. Naltrexone at low doses upregulates a unique gene expression not seen with normal doses: Implications for its use in cancer therapy. Int J Oncol. 2016 Aug;49(2):793-802. doi: 10.3892/ijo.2016.3567. Epub 2016 Jun 7. PMID: 27279602.
Naltrexone at low doses upregulates a unique gene expression not seen with normal doses: Implications for its use in cancer therapy
Lower doses of naltrexone (LDN) have been shown to inhibit tumor growth by altering cell signaling and immune system responses, as evidenced by changes in gene expression related to cell cycle regulation and apoptosis. Adjusting treatment schedules—specifically including a drug-free phase after initial LDN exposure—enhanced the drug’s efficacy, increasing sensitivity to chemotherapy agents like oxaliplatin. Overall, the findings suggest that LDN may have anticancer properties that can be optimized through treatment modifications.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/27279602/.
Donahue RN, McLaughlin PJ, Zagon IS. Low-dose naltrexone suppresses ovarian cancer and exhibits enhanced inhibition in combination with cisplatin. Exp Biol Med (Maywood). 2011 Jul;236(7):883-95. doi: 10.1258/ebm.2011.011096. Epub 2011 Jun 17. PMID: 21685240.
Low-dose naltrexone suppresses ovarian cancer and exhibits enhanced inhibition in combination with cisplatin
Ovarian cancer is a leading cause of gynecological cancer death, with 65% of patients relapsing after initial treatment. This study investigates the effects of the opioid antagonist naltrexone (NTX) on ovarian cancer cell proliferation and tumor progression. It found that intermittent NTX administration reduced cell replication in vitro and tumor growth in mice, especially when combined with cisplatin, while also decreasing the toxicity of cisplatin. The results suggest that the OGF-OGFr axis plays a crucial role in the anti-cancer effects of NTX and low-dose naltrexone (LDN), indicating a potential non-toxic treatment option for ovarian cancer patients.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/21685240/.
Liu N, Yan L, Shan F, Wang X, Qu N, Handley MK, Ma M. Low-dose naltrexone plays antineoplastic role in cervical cancer progression through suppressing PI3K/AKT/mTOR pathway. Transl Oncol. 2021 Apr;14(4):101028. doi: 10.1016/j.tranon.2021.101028. Epub 2021 Feb 1. PMID: 33540155; PMCID: PMC7859308.
Low-dose naltrexone plays antineoplastic role in cervical cancer progression through suppressing PI3K/AKT/mTOR pathway
The incidence of cervical cancer is rising globally, and low-dose naltrexone (LDN) has shown potential in delaying tumor progression by upregulating OGFr and inhibiting colony formation, migration, and invasion in cervical cancer cells. LDN also reduced the expression of key signaling pathways (PI3K, pAKT, and mTOR) in both cell cultures and mouse models, suggesting it may be a promising treatment option for cervical cancer.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/33540155/.
Liu N, Ma M, Qu N, Wang R, Chen H, Hu F, Gao S, Shan F. Low-dose naltrexone inhibits the epithelial-mesenchymal transition of cervical cancer cells in vitro and effects indirectly on tumor-associated macrophages in vivo. Int Immunopharmacol. 2020 Sep;86:106718. doi: 10.1016/j.intimp.2020.106718. Epub 2020 Jun 22. PMID: 32585612.
Low-dose naltrexone inhibits the epithelial-mesenchymal transition of cervical cancer cells in vitro and effects indirectly on tumor-associated macrophages in vivo
The study found that low-dose naltrexone (LDN) inhibits the progression of cervical cancer by suppressing the proliferation, migration, and invasion of Hela cells and promoting apoptosis, effects that are reversed by silencing the opioid growth factor receptor (OGFr). In vivo, LDN reduced tumor-associated macrophages, particularly M2 macrophages, and decreased the anti-inflammatory cytokine IL-10, suggesting its potential as a treatment for cervical cancer.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/32585612/.
Raknes G, Småbrekke L. Low dose naltrexone in multiple sclerosis: Effects on medication use. A quasi-experimental study. PLoS One. 2017 Nov 3;12(11):e0187423. doi: 10.1371/journal.pone.0187423. PMID: 29099849; PMCID: PMC5669439.
Low dose naltrexone in multiple sclerosis: Effects on medication use. A quasi-experimental study
Low dose naltrexone (LDN) is gaining attention as an off-label treatment for multiple sclerosis (MS), with some small studies suggesting it may be beneficial. A quasi-experimental study in Norway investigated whether a rise in LDN use in 2013 led to changes in the dispensing of other MS medications. Despite tracking 341 patients and analyzing over 20,000 prescriptions, the study found no significant differences in the use of disease-modifying therapies or symptom management medications before and after LDN initiation, apart from general trends in MS therapy.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/29099849/.
Muller G, Grieshaber R, Talley JF, Riepl M, Fellows D. Compounded Low-dose Naltrexone for the Treatment of Guttate Psoriasis: A Case Report. Int J Pharm Compd. 2018 Jul-Aug;22(4):270-278. PMID: 30021181.
Compounded Low-dose Naltrexone for the Treatment of Guttate Psoriasis: A Case Report
This article presents a case study of a 75-year-old man with guttate psoriasis successfully treated with a compounded formulation of oral low-dose naltrexone, which resulted in minimal side effects and was cost-effective, highlighting its potential as an alternative therapy for autoimmune skin conditions like psoriasis, often overlooked by clinicians.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/30021181/.
Jaros J, Lio P. Low Dose Naltrexone in Dermatology. J Drugs Dermatol. 2019 Mar 1;18(3):235-238. PMID: 30909326.
Low Dose Naltrexone in Dermatology
Low-dose naltrexone (LDN) has been studied as an effective immunomodulatory and anti-inflammatory treatment for various conditions, including Crohn’s disease, fibromyalgia, and multiple sclerosis, and has recently shown promise in improving dermatologic issues such as systemic sclerosis and guttate psoriasis, with a focus on its potential application for atopic dermatitis.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/30909326/.
Varghese K, Yan X, Cao F. Low-Dose Naltrexone for Excoriation Disorder. Cureus. 2024 Mar 1;16(3):e55336. doi: 10.7759/cureus.55336. PMID: 38559544; PMCID: PMC10981904.
Low-Dose Naltrexone for Excoriation Disorder
Excoriation disorder (ED) involves compulsively picking at the skin, leading to physical and psychological distress, and while higher doses of naltrexone have been previously reported as effective, this case study presents the first documented improvement of ED symptoms in a patient treated with low-dose naltrexone (LDN) at 4.5 mg, demonstrating significant symptom relief after three months of treatment and worsening symptoms upon interruption, suggesting LDN’s potential therapeutic benefit for ED.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/38559544/.
Shabeeb N. The lowdown on low-dose naltrexone. Cutis. 2020 Jan;105(1):E17-E18. PMID: 32074159.
The lowdown on low-dose naltrexone
Low-dose naltrexone (LDN) is gaining attention in dermatology as an off-label treatment for inflammatory skin conditions, offering an alternative to traditional systemic therapies. Dermatologists should understand its mechanism, prescribing guidelines, and potential side effects to address patient inquiries effectively.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/32074159/.
Albers LN, Arbiser JL, Feldman RJ. Treatment of Hailey-Hailey Disease With Low-Dose Naltrexone. JAMA Dermatol. 2017 Oct 1;153(10):1018-1020. doi: 10.1001/jamadermatol.2017.2446. Erratum in: JAMA Dermatol. 2017 Oct 1;153(10):1072. doi: 10.1001/jamadermatol.2017.3904. PMID: 28768313; PMCID: PMC5817589.
Treatment of Hailey-Hailey Disease With Low-Dose Naltrexone
A case series involving three patients with severe Hailey-Hailey disease, resistant to multiple therapies, demonstrated that low-dose naltrexone (3-4.5 mg nightly) significantly healed skin lesions within 1-2 weeks and led to clinical resolution within two months. Discontinuation resulted in symptom flare-ups that resolved quickly upon re-administration, suggesting low-dose naltrexone may be an effective new treatment for this condition, potentially enhancing keratinocyte differentiation and wound healing. Further research is needed to clarify its mechanisms and therapeutic role.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/28768313/.
Yang J, Shin KM, Do A, Bierle DM, Abu Dabrh AM, Yin Z, Bauer BA, Mohabbat AB. The Safety and Efficacy of Low-Dose Naltrexone in Patients with Fibromyalgia: A Systematic Review. J Pain Res. 2023 Mar 21;16:1017-1023. doi: 10.2147/JPR.S395457. PMID: 36974308; PMCID: PMC10039621.
The Safety and Efficacy of Low-Dose Naltrexone in Patients with Fibromyalgia: A Systematic Review
Fibromyalgia (FM) is a chronic pain condition marked by widespread musculoskeletal pain, and low-dose naltrexone (LDN) is being explored as an off-label treatment option. A systematic review of the literature identified nine studies, including one randomized controlled trial, suggesting that LDN may be effective for symptom management in FM, with no severe adverse events reported in 78% of the studies that assessed safety. However, the overall evidence remains limited due to methodological differences among studies, highlighting the need for more rigorous trials to confirm LDN’s efficacy and safety.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/36974308/.
McKenzie-Brown AM, Boorman DW, Ibanez KR, Agwu E, Singh V. Low-Dose Naltrexone (LDN) for Chronic Pain at a Single Institution: A Case Series. J Pain Res. 2023 Jun 14;16:1993-1998. doi: 10.2147/JPR.S389957. PMID: 37337611; PMCID: PMC10276990.
Low-Dose Naltrexone (LDN) for Chronic Pain at a Single Institution: A Case Series
A review of patient charts from a Pain Center found that low-dose naltrexone (LDN) may effectively alleviate chronic pain, particularly in conditions like neuropathic pain and complex regional pain syndrome, with 64% of patients reporting some relief. However, a significant portion of patients either did not fill their prescriptions or were unresponsive, particularly those diagnosed with spondylosis. Overall, neuropathic pain patients experienced greater benefits from LDN compared to those with other pain diagnoses, indicating a need for trials lasting several weeks to observe analgesic effects.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/37337611/.
Dieckmann G, Ozmen MC, Cox SM, Engert RC, Hamrah P. Low-dose naltrexone is effective and well-tolerated for modulating symptoms in patients with neuropathic corneal pain. Ocul Surf. 2021 Apr;20:33-38. doi: 10.1016/j.jtos.2020.12.003. Epub 2021 Jan 12. PMID: 33450415; PMCID: PMC9009761.
Low-dose naltrexone is effective and well-tolerated for modulating symptoms in patients with neuropathic corneal pain
This retrospective study evaluated the effectiveness and tolerability of low-dose naltrexone (LDN) in treating refractory neuropathic corneal pain (NCP) in 30 patients. After at least four weeks of LDN treatment, patients experienced a significant 49.22% reduction in mean pain scores and improved quality of life, with common side effects including vivid dreams, headaches, and stomachache. The findings suggest that LDN is both effective and well-tolerated for managing NCP.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/33450415/.
Lee MW, Fujioka K. Naltrexone for the treatment of obesity: review and update. Expert Opin Pharmacother. 2009 Aug;10(11):1841-5. doi: 10.1517/14656560903048959. PMID: 19537999.
Naltrexone for the treatment of obesity: review and update. Expert Opin Pharmacother
Endogenous opioid peptides regulate food intake, as shown in animal and human studies. While naltrexone alone causes minimal weight loss, its combination with bupropion may be effective for obesity treatment.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/19537999/.
Kulak-Bejda A, Bejda G, Waszkiewicz N. Safety and efficacy of naltrexone for weight loss in adult patients – a systematic review. Arch Med Sci. 2020 Sep 10;17(4):940-953. doi: 10.5114/aoms.2020.96908. PMID: 34336024; PMCID: PMC8314402.
Safety and efficacy of naltrexone for weight loss in adult patients – a systematic review
This systematic review analyzed 14 studies on the safety and efficacy of naltrexone and naltrexone/bupropion for weight loss, finding that the treatment is effective and generally well-tolerated in promoting weight loss in obese patients, with side effects rarely reported.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/34336024/.
Makowski CT, Gwinn KM, Hurren KM. Naltrexone/bupropion: an investigational combination for weight loss and maintenance. Obes Facts. 2011;4(6):489-94. doi: 10.1159/000335352. Epub 2011 Dec 15. PMID: 22249001; PMCID: PMC6444555.
Naltrexone/bupropion: an investigational combination for weight loss and maintenance
Naltrexone/bupropion, an investigational combination for weight loss in obese or overweight patients, showed a placebo-subtracted weight loss of 4.7% after one year in phase 3 trials, along with improvements in waist circumference, insulin resistance, and HbA1c in diabetic patients. Common side effects include nausea and constipation, with further studies needed to assess cardiovascular outcomes.
You can read the abstract of this article at
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6444555/.
Apovian CM. Naltrexone/bupropion for the treatment of obesity and obesity with Type 2 diabetes. Future Cardiol. 2016 Mar;12(2):129-38. doi: 10.2217/fca.15.79. Epub 2015 Dec 18. PMID: 26679384.
Naltrexone/bupropion for the treatment of obesity and obesity with Type 2 diabetes. Future Cardiol
Contrave, a combination of naltrexone and bupropion, has been shown to promote significant weight loss in four Phase III clinical trials involving 4,536 adults. Over 52 weeks, patients lost an average of 11-22 lbs, with improvements in cardiometabolic markers.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/26679384/.
McIntyre RS, Paron E, Burrows M, Blavignac J, Gould E, Camacho F, Barakat M. Psychiatric Safety and Weight Loss Efficacy of Naltrexone/bupropion as Add-on to Antidepressant Therapy in Patients with Obesity or Overweight. J Affect Disord. 2021 Jun 15;289:167-176. doi: 10.1016/j.jad.2021.04.017. Epub 2021 Apr 23. PMID: 33989969.
Psychiatric Safety and Weight Loss Efficacy of Naltrexone/bupropion as Add-on to Antidepressant Therapy in Patients with Obesity or Overweight
This study analyzed the safety and efficacy of Naltrexone/Bupropion (NB) for weight loss in individuals with obesity, with or without antidepressant use. Results showed that NB was effective in promoting weight loss, particularly in those not on antidepressants, and was well tolerated regardless of antidepressant use.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/33989969/.
Atkinson RL, Berke LK, Drake CR, Bibbs ML, Williams FL, Kaiser DL. Effects of long-term therapy with naltrexone on body weight in obesity. Clin Pharmacol Ther. 1985 Oct;38(4):419-22. doi: 10.1038/clpt.1985.197. PMID: 4042525.
Williams FL, Kaiser DL. Effects of long-term therapy with naltrexone on body weight in obesity
A study on 60 obese individuals found that naltrexone (50 or 100 mg) did not significantly impact overall weight loss compared to placebo, though women experienced modest weight loss. Side effects were mild, but some participants had abnormal liver function tests. Further research on naltrexone’s effects on weight loss is recommended.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/4042525/.
Christou GA, Kiortsis DN. The efficacy and safety of the naltrexone/bupropion combination for the treatment of obesity: an update. Hormones (Athens). 2015 Jul-Sep;14(3):370-5. doi: 10.14310/horm.2002.1600. PMID: 26188223.
The efficacy and safety of the naltrexone/bupropion combination for the treatment of obesity: an update
The combination of naltrexone and bupropion (NB32) has been approved as an adjunct to lifestyle interventions for weight loss, showing 5-9% reduction in body weight and improvements in metabolic markers over 56 weeks. Common side effects include nausea and headache, with serious adverse events being rare.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/26188223/.
Onakpoya IJ, Lee JJ, Mahtani KR, Aronson JK, Heneghan CJ. Naltrexone-bupropion (Mysimba) in management of obesity: A systematic review and meta-analysis of unpublished clinical study reports. Br J Clin Pharmacol. 2020 Apr;86(4):646-667. doi: 10.1111/bcp.14210. Epub 2020 Feb 4. Erratum in: Br J Clin Pharmacol. 2024 Jun;90(6):1531-1533. doi: 10.1111/bcp.16065. PMID: 31918448; PMCID: PMC7098870.
Naltrexone-bupropion (Mysimba) in management of obesity: A systematic review and meta-analysis of unpublished clinical study reports
This study analyzed data from four pivotal trials to assess the benefits and harms of naltrexone-bupropion for weight loss. While the drug led to a modest reduction in body weight, it also significantly increased the risk of adverse events, including serious side effects and treatment discontinuation. The quality of evidence was mostly low to moderate, and further postmarketing surveillance is recommended.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/31918448/.
le Roux CW, Fils-Aimé N, Camacho F, Gould E, Barakat M. The relationship between early weight loss and weight loss maintenance with naltrexone-bupropion therapy. EClinicalMedicine. 2022 May 27;49:101436. doi: 10.1016/j.eclinm.2022.101436. PMID: 35747175; PMCID: PMC9156890.
The relationship between early weight loss and weight loss maintenance with naltrexone-bupropion therapy
Extended-release naltrexone/bupropion (NB) was found to result in greater weight loss maintenance than placebo in several trials, with statistically significant results for maintaining ≥5% and ≥10% weight loss over periods of up to 208 weeks, suggesting its potential for long-term weight loss strategies.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/35747175/.
Hong K, Herrmann K, Dybala C, Halseth AE, Lam H, Foreyt JP. Naltrexone/Bupropion extended release-induced weight loss is independent of nausea in subjects without diabetes. Clin Obes. 2016 Oct;6(5):305-12. doi: 10.1111/cob.12157. Epub 2016 Aug 1. PMID: 27477337; PMCID: PMC5129540.
Naltrexone/Bupropion extended release-induced weight loss is independent of nausea in subjects without diabetes. Clin
Naltrexone/bupropion extended release (NB) aids chronic weight management in adults with a high BMI and related comorbidities. In phase 3 studies, NB led to more weight loss than placebo, though nausea, mostly mild to moderate, was more common in NB-treated subjects, peaking in week 1. Nausea had no significant effect on weight loss.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/27477337/.
Greenway FL, Fujioka K, Plodkowski RA, Mudaliar S, Guttadauria M, Erickson J, Kim DD, Dunayevich E; COR-I Study Group. Effect of naltrexone plus bupropion on weight loss in overweight and obese adults (COR-I): a multicentre, randomised, double-blind, placebo-controlled, phase 3 trial. Lancet. 2010 Aug 21;376(9741):595-605. doi: 10.1016/S0140-6736(10)60888-4. Epub 2010 Jul 29. Erratum in: Lancet. 2010 Aug 21;376(9741):594. Erratum in: Lancet. 2010 Oct 23;376(9750):1392. PMID: 20673995.
Effect of naltrexone plus bupropion on weight loss in overweight and obese adults (COR-I): a multicentre, randomised, double-blind, placebo-controlled, phase 3 trial
The COR-I study evaluated the effectiveness of a sustained-release combination of naltrexone and bupropion for weight loss in overweight and obese adults. Participants taking the drug combination experienced significantly greater weight loss compared to placebo, with 48% achieving at least 5% weight loss at the highest dose. Common side effects included nausea, headache, and constipation. The combination therapy showed a slight initial rise in blood pressure but did not increase depression or suicidality, making it a potential treatment option for obesity.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/20673995/.
Liu Y, Han F, Xia Z, Sun P, Rohani P, Amirthalingam P, Sohouli MH. The effects of bupropion alone and combined with naltrexone on weight loss: a systematic review and meta-regression analysis of randomized controlled trials. Diabetol Metab Syndr. 2024 Apr 24;16(1):93. doi: 10.1186/s13098-024-01319-7. PMID: 38658994; PMCID: PMC11044307.
The effects of bupropion alone and combined with naltrexone on weight loss: a systematic review and meta-regression analysis of randomized controlled trials
This study conducted a meta-analysis of 25 trials involving 22,165 participants to evaluate the effects of bupropion alone and in combination with naltrexone on weight loss, BMI, and waist circumference. The findings showed that both interventions significantly reduced weight and waist circumference, with the combination therapy proving more effective than bupropion alone.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/38658994/.
Welling MS, Mohseni M, van der Valk ES, van Hagen JM, Burgerhart JS, van Haelst MM, van Rossum EFC. Successful naltrexone-bupropion treatment after several treatment failures in a patient with severe monogenic obesity. iScience. 2023 Feb 14;26(3):106199. doi: 10.1016/j.isci.2023.106199. PMID: 36876127; PMCID: PMC9982263.
Successful naltrexone-bupropion treatment after several treatment failures in a patient with severe monogenic obesity
A 33-year-old patient with early-onset obesity (BMI 56.7 kg/m²) and hyperphagia due to a likely pathogenic MC4R gene variant experienced unsuccessful treatments with lifestyle interventions, surgery, liraglutide, and metformin. However, naltrexone-bupropion treatment led to significant weight loss (-48.9 kg) and improved hyperphagia and quality of life over 17 months, highlighting its potential for managing genetic obesity after other treatments fail.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/36876127/.
Apovian CM, Aronne L, Rubino D, Still C, Wyatt H, Burns C, Kim D, Dunayevich E; COR-II Study Group. A randomized, phase 3 trial of naltrexone SR/bupropion SR on weight and obesity-related risk factors (COR-II). Obesity (Silver Spring). 2013 May;21(5):935-43. doi: 10.1002/oby.20309. PMID: 23408728; PMCID: PMC3739931.
COR-II Study Group. A randomized, phase 3 trial of naltrexone SR/bupropion SR on weight and obesity-related risk factors (COR-II)
The study examined the effects of naltrexone/bupropion (NB) combination therapy on weight loss in overweight and obese participants, finding significantly greater weight loss and improvements in cardiometabolic risk factors and quality of life with NB compared to placebo over 56 weeks, with nausea being the most common mild to moderate side effect.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/23408728/.
Carbone EA, Caroleo M, Rania M, Calabrò G, Staltari FA, de Filippis R, Aloi M, Condoleo F, Arturi F, Segura-Garcia C. An open-label trial on the efficacy and tolerability of naltrexone/bupropion SR for treating altered eating behaviours and weight loss in binge eating disorder. Eat Weight Disord. 2021 Apr;26(3):779-788. doi: 10.1007/s40519-020-00910-x. Epub 2020 Apr 30. PMID: 32356145.
An open-label trial on the efficacy and tolerability of naltrexone/bupropion SR for treating altered eating behaviours and weight loss in binge eating disorder
This preliminary study evaluated the efficacy of a combination of naltrexone and bupropion (NB) for improving pathological eating behavior and weight loss in obese patients with binge eating disorder (BED). In a sample of 23 obese-BED patients and 20 obese non-BED controls, both groups experienced significant weight loss (≈8% ΔBMI) and improvements in binge eating behaviors after 16 weeks of treatment, with better results in the BED group. The treatment was well-tolerated, suggesting that NB, alongside lifestyle modifications, could be an effective option for managing BED and obesity.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/32356145/.
Barrea L, Pugliese G, Muscogiuri G, Laudisio D, Colao A, Savastano S. New-generation anti-obesity drugs: naltrexone/bupropion and liraglutide. An update for endocrinologists and nutritionists. Minerva Endocrinol. 2020 Jun;45(2):127-137. doi: 10.23736/S0391-1977.20.03179-X. PMID: 32643356.
New-generation anti-obesity drugs: naltrexone/bupropion and liraglutide
The global rise in obesity poses significant economic challenges for healthcare systems, necessitating effective management strategies. While lifestyle modifications like diet and exercise are the primary methods for achieving weight loss, long-term maintenance remains difficult, leading to weight regain. Consequently, pharmacological interventions, particularly the new-generation anti-obesity drugs naltrexone/bupropion and liraglutide, have emerged as valuable adjuncts to lifestyle changes. These medications target specific areas of the brain to enhance weight loss outcomes, and ongoing research is also exploring semaglutide for future obesity treatment.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/32643356/.
Billes SK, Sinnayah P, Cowley MA. Naltrexone/bupropion for obesity: an investigational combination pharmacotherapy for weight loss. Pharmacol Res. 2014 Jun;84:1-11. doi: 10.1016/j.phrs.2014.04.004. Epub 2014 Apr 19. PMID: 24754973.
Naltrexone/bupropion for obesity: an investigational combination pharmacotherapy for weight loss
The combination therapy of naltrexone/bupropion (NB) for obesity targets alterations in the hypothalamic melanocortin and brain reward systems to influence food intake and cravings, addressing the complex challenges of achieving long-term weight loss. Despite the lack of fully understood mechanisms, current research highlights NB’s potential effectiveness through its actions on these brain regions, supported by various in vitro, in vivo, and clinical studies.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/24754973/.
Green R, Bujarski S, Lim AC, Venegas A, Ray LA. Naltrexone and alcohol effects on craving for cigarettes in heavy drinking smokers. Exp Clin Psychopharmacol. 2019 Jun;27(3):257-264. doi: 10.1037/pha0000252. Epub 2019 Jan 10. PMID: 30628813; PMCID: PMC7227763.
Naltrexone and alcohol effects on craving for cigarettes in heavy drinking smokers
A study investigated the effects of naltrexone on cigarette and alcohol cravings among heavy drinking smokers of East Asian descent, revealing that naltrexone significantly reduced cravings for both substances during alcohol administration. The research, conducted with a double-blind placebo-controlled design involving 31 participants, found that while cravings for cigarettes and alcohol increased with alcohol intake, naltrexone effectively blunted these cravings, suggesting its potential benefit for this specific group. Further clinical studies are needed to explore these findings.
You can read the abstract of this article at
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7227763/.
King AC, Cao D, O’Malley SS, Kranzler HR, Cai X, deWit H, Matthews AK, Stachoviak RJ. Effects of naltrexone on smoking cessation outcomes and weight gain in nicotine-dependent men and women. J Clin Psychopharmacol. 2012 Oct;32(5):630-6. doi: 10.1097/JCP.0b013e3182676956. PMID: 22926596; PMCID: PMC4640209.
Effects of naltrexone on smoking cessation outcomes and weight gain in nicotine-dependent men and women
This study found that naltrexone improved short-term quit rates, reduced smoking urges, and lessened weight gain in nicotine-dependent individuals during treatment, with men experiencing greater smoking reductions and women benefiting more in weight control. However, its effect on smoking cessation was not sustained after discontinuation.
You can read the abstract of this article at
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4640209/.
Mooney ME, Schmitz JM, Allen S, Grabowski J, Pentel P, Oliver A, Hatsukami DK. Bupropion and naltrexone for smoking cessation: A double-blind randomized placebo-controlled clinical trial. Clin Pharmacol Ther. 2016 Oct;100(4):344-52. doi: 10.1002/cpt.402. Epub 2016 Jun 20. PMID: 27213949; PMCID: PMC5017904.
Bupropion and naltrexone for smoking cessation: A double-blind randomized placebo-controlled clinical trial
A study on smoking cessation compared bupropion (BUP) with and without naltrexone (NTX) in 121 smokers over 7 weeks. The BUP + NTX group had higher abstinence rates at 7 weeks but not at 6 months. NTX reduced nicotine withdrawal, though both groups experienced similar retention and some side effects.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/27213949/.
Toll BA, White M, Wu R, Meandzija B, Jatlow P, Makuch R, O’Malley SS. Low-dose naltrexone augmentation of nicotine replacement for smoking cessation with reduced weight gain: a randomized trial. Drug Alcohol Depend. 2010 Oct 1;111(3):200-6. doi: 10.1016/j.drugalcdep.2010.04.015. Epub 2010 Jun 12. PMID: 20542391; PMCID: PMC3771701.
Low-dose naltrexone augmentation of nicotine replacement for smoking cessation with reduced weight gain: a randomized trial
This study tested whether 25 mg naltrexone could minimize post-quit weight gain and improve smoking cessation outcomes in smokers concerned about weight gain. After 27 weeks, naltrexone did not significantly reduce weight gain or improve smoking abstinence rates compared to placebo, suggesting that its small impact on weight gain is not enough to justify potential effects on quitting success.
You can read the abstract of this article at
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3771701/.
Ray LA, Green R, Enders C, Leventhal AM, Grodin EN, Li G, Lim A, Hartwell E, Venegas A, Meredith L, Nieto SJ, Shoptaw S, Ho D, Miotto K. Efficacy of Combining Varenicline and Naltrexone for Smoking Cessation and Drinking Reduction: A Randomized Clinical Trial. Am J Psychiatry. 2021 Sep 1;178(9):818-828. doi: 10.1176/appi.ajp.2020.20070993. Epub 2021 Jun 3. PMID: 34080890; PMCID: PMC8999864.
Efficacy of Combining Varenicline and Naltrexone for Smoking Cessation and Drinking Reduction: A Randomized Clinical Trial
This study compared varenicline plus naltrexone to varenicline alone for smoking cessation and drinking reduction in heavy-drinking smokers. While varenicline alone was more effective for smoking cessation at 26 weeks, the combination of varenicline and naltrexone showed a non-significant trend towards reducing alcohol consumption during the 12-week treatment phase.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/34080890/.
Covey LS, Glassman AH, Stetner F. Naltrexone effects on short-term and long-term smoking cessation. J Addict Dis. 1999;18(1):31-40. doi: 10.1300/J069v18n01_04. PMID: 10234561.
Naltrexone effects on short-term and long-term smoking cessation
This study investigated the efficacy of naltrexone in smoking cessation, finding it increased quit rates and reduced weight gain during treatment, with men showing greater reductions in smoking and women experiencing more weight control. However, the benefits diminished after treatment stopped, and further research into sex differences is needed.
You can read the abstract of this article at
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4640209/.
King A, Cao D, Zhang L, Rueger SY. Effects of the opioid receptor antagonist naltrexone on smoking and related behaviors in smokers preparing to quit: a randomized controlled trial. Addiction. 2013 Oct;108(10):1836-44. doi: 10.1111/add.12261. Epub 2013 Jul 12. PMID: 23714324; PMCID: PMC3775903.
Effects of the opioid receptor antagonist naltrexone on smoking and related behaviors in smokers preparing to quit: a randomized controlled trial
This study investigated the effects of naltrexone on smoking behaviors in smokers preparing to quit. In a double-blind, placebo-controlled trial, 315 participants were observed during a pre-quit phase. Naltrexone significantly reduced cigarette consumption, smoking urges, and alcohol intake compared to placebo, and these reductions predicted similar post-quit outcomes, suggesting naltrexone’s pre-quit effects may mediate post-quit success.
You can read the abstract of this article at
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3775903/.
Lyu X, Du J, Zhan G, Wu Y, Su H, Zhu Y, Jarskog F, Zhao M, Fan X. Naltrexone and Bupropion Combination Treatment for Smoking Cessation and Weight Loss in Patients With Schizophrenia. Front Pharmacol. 2018 Mar 5;9:181. doi: 10.3389/fphar.2018.00181. PMID: 29563871; PMCID: PMC5850123.
Naltrexone and Bupropion Combination Treatment for Smoking Cessation and Weight Loss in Patients With Schizophrenia
This study investigated the effects of naltrexone on smoking behaviors in smokers preparing to quit. In a double-blind, placebo-controlled trial, 315 participants were observed during a pre-quit phase. Naltrexone significantly reduced cigarette consumption, smoking urges, and alcohol intake compared to placebo, and these reductions predicted similar post-quit outcomes, suggesting naltrexone’s pre-quit effects may mediate post-quit success.
You can read the abstract of this article at
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5850123/.
Kahler CW, Cioe PA, Tzilos GK, Spillane NS, Leggio L, Ramsey SE, Brown RA, O’Malley SS. A Double-Blind Randomized Placebo-Controlled Trial of Oral Naltrexone for Heavy-Drinking Smokers Seeking Smoking Cessation Treatment. Alcohol Clin Exp Res. 2017 Jun;41(6):1201-1211. doi: 10.1111/acer.13396. Epub 2017 May 7. PMID: 28401564; PMCID: PMC5485847.
A Double-Blind Randomized Placebo-Controlled Trial of Oral Naltrexone for Heavy-Drinking Smokers Seeking Smoking Cessation Treatment
This study found that while heavy-drinking smokers reduced their alcohol consumption and smoking during a cessation program, naltrexone did not significantly enhance these reductions compared to placebo. The study concluded that naltrexone was not effective for improving smoking cessation or reducing drinking in this population.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/28401564/
Fridberg DJ, Cao D, Grant JE, King AC. Naltrexone improves quit rates, attenuates smoking urge, and reduces alcohol use in heavy drinking smokers attempting to quit smoking. Alcohol Clin Exp Res. 2014 Oct;38(10):2622-9. doi: 10.1111/acer.12513. Epub 2014 Oct 21. PMID: 25335648; PMCID: PMC4638321.
Naltrexone improves quit rates, attenuates smoking urge, and reduces alcohol use in heavy drinking smokers attempting to quit smoking
This study examined whether naltrexone could improve smoking cessation outcomes in smokers with varying drinking patterns. It found that heavy drinking smokers (HDS) benefited significantly from naltrexone, showing higher quit rates, reduced smoking urges, and decreased alcohol use, while moderate-to-light and nondrinking smokers did not experience the same effects. Naltrexone’s impact on reducing smoking urge in the early weeks of treatment mediated its effect on smoking abstinence in HDS, highlighting this group as an important target for adjunctive naltrexone treatment.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/25335648/.
Brauer LH, Behm FM, Westman EC, Patel P, Rose JE. Naltrexone blockade of nicotine effects in cigarette smokers. Psychopharmacology (Berl). 1999 Apr;143(4):339-46. doi: 10.1007/s002130050957. PMID: 10367550.
Naltrexone blockade of nicotine effects in cigarette smokers
This study investigated the effects of naltrexone and nicotine on smoking behavior. It found that nicotine reduced craving and negative affect while naltrexone blocked these effects, suggesting a role for opioid mechanisms in smoking.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/10367550/.
Walsh Z, Epstein A, Munisamy G, King A. The impact of depressive symptoms on the efficacy of naltrexone in smoking cessation. J Addict Dis. 2008;27(1):65-72. doi: 10.1300/J069v27n01_07. PMID: 18551889.
The impact of depressive symptoms on the efficacy of naltrexone in smoking cessation
This study examined mood changes in newly abstinent opioid-dependent individuals undergoing naltrexone treatment. Over four weeks, depression scores significantly improved, though “late insomnia” increased temporarily at two weeks. Overall, naltrexone did not worsen depression but may affect early sleep patterns.
You can read the abstract of this article at
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3111044/.
Krishnan-Sarin S, Meandzija B, O’Malley S. Naltrexone and nicotine patch smoking cessation: a preliminary study. Nicotine Tob Res. 2003 Dec;5(6):851-7. doi: 10.1080/14622200310001614601. PMID: 14750508.
Naltrexone and nicotine patch smoking cessation: a preliminary study. Nicotine Tob Res
This preliminary study suggests that adding 50 mg of naltrexone to nicotine replacement therapy may improve smoking cessation outcomes by increasing abstinence rates, reducing relapse, decreasing the desire to smoke, and preventing post-cessation weight gain.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/14750508/.
Toll BA, Leary V, Wu R, Salovey P, Meandzija B, O’Malley SS. A preliminary investigation of naltrexone augmentation of bupropion to stop smoking with less weight gain. Addict Behav. 2008 Jan;33(1):173-9. doi: 10.1016/j.addbeh.2007.05.012. Epub 2007 Jun 2. PMID: 17587504; PMCID: PMC2488403.
A preliminary investigation of naltrexone augmentation of bupropion to stop smoking with less weight gain
An open-label study examined the effects of naltrexone (25 mg/day) combined with bupropion (300 mg/day) on smoking cessation and weight gain in weight-concerned smokers. In a sample of 20 participants compared to 20 controls receiving bupropion alone, results showed no significant differences in smoking abstinence rates. However, those in the naltrexone+bupropion group experienced less weight gain (mean=1.67 lb) compared to the bupropion-only group (mean=3.17 lb). While not statistically significant, the findings suggest that this combination may help mitigate post-cessation weight gain and warrant further investigation in larger studies.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/17587504/.
Schmitz JM, Stotts AL, Yoon JH, Northrup TF, Villarreal YR, Yammine L, Weaver MF, Carmody T, Shoptaw S, Trivedi MH. Naltrexone plus bupropion reduces cigarette smoking in individuals with methamphetamine use disorder: A secondary analysis from the CTN ADAPT-2 trial. J Subst Use Addict Treat. 2023 Aug;151:208987. doi: 10.1016/j.josat.2023.208987. Epub 2023 Feb 21. PMID: 36822269; PMCID: PMC11008704.
Naltrexone plus bupropion reduces cigarette smoking in individuals with methamphetamine use disorder: A secondary analysis from the CTN ADAPT-2 trial
The ADAPT-2 study examined the effects of naltrexone plus bupropion (NTX-BUP) on cigarette smoking in participants with methamphetamine use disorder. Among 403 participants, 290 were smokers, and those treated with NTX-BUP showed significant improvements in smoking outcomes compared to placebo, indicating that NTX-BUP may effectively reduce cigarette smoking alongside methamphetamine treatment and highlighting its potential as a co-addiction strategy for public health benefits.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/36822269/.
Anton RF, Latham PK, Voronin KE, Randall PK, Book SW, Hoffman M, Schacht JP. Nicotine-Use/Smoking Is Associated with the Efficacy of Naltrexone in the Treatment of Alcohol Dependence. Alcohol Clin Exp Res. 2018 Apr;42(4):751-760. doi: 10.1111/acer.13601. Epub 2018 Feb 12. PMID: 29431852; PMCID: PMC5880727.
Nicotine-Use/Smoking Is Associated with the Efficacy of Naltrexone in the Treatment of Alcohol Dependence
This study found that nicotine use/smoking status significantly predicts naltrexone’s effectiveness in reducing alcohol consumption among individuals with alcohol dependence. Smokers experienced greater reductions in heavy drinking when treated with naltrexone compared to placebo, while non-smokers showed no significant difference. Nicotine use was a stronger predictor of response than the OPRM1 A118G genotype. Smoking behavior itself was not influenced by naltrexone during the trial.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/29431852/.
Ward S, Smith N, Bowden-Jones H. The use of naltrexone in pathological and problem gambling: A UK case series. J Behav Addict. 2018 Sep 1;7(3):827-833. doi: 10.1556/2006.7.2018.89. Epub 2018 Sep 21. PMID: 30238780; PMCID: PMC6426388.
The use of naltrexone in pathological and problem gambling: A UK case series
This study explored the use of naltrexone to treat problem gamblers who had not responded to psychological therapies. Of 14 patients treated, 60% abstained from gambling, while 20% significantly reduced their gambling. Side effects included gastrointestinal issues and dizziness, and two patients with alcohol-use disorder relapsed during treatment. Care is advised when prescribing to those with alcohol-use disorder.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/30238780/.
Nestor LJ, Paterson LM, Murphy A, McGonigle J, Orban C, Reed L, Taylor E, Flechais R, Smith D, Bullmore ET, Ersche KD, Suckling J, Elliott R, Deakin B, Rabiner I, Lingford Hughes A, Sahakian BJ, Robbins TW, Nutt DJ; ICCAM Consortium. Naltrexone differentially modulates the neural correlates of motor impulse control in abstinent alcohol-dependent and polysubstance-dependent individuals. Eur J Neurosci. 2019 Aug;50(3):2311-2321. doi: 10.1111/ejn.14262. Epub 2018 Nov 26. PMID: 30402987; PMCID: PMC6767584.
Naltrexone differentially modulates the neural correlates of motor impulse control in abstinent alcohol-dependent and polysubstance-dependent individuals. Eur J Neurosci
This study examines how acute naltrexone affects neural responses during motor impulse control in abstinent alcohol-dependent (AUD) and polysubstance-dependent (poly-SUD) individuals. While there were no task performance differences, the AUD group showed greater brain activation in prefrontal areas compared to controls, with effects linked to alcohol abstinence. Naltrexone enhanced activity in different brain regions (orbitofrontal cortex for AUD, anterior insula for poly-SUD), and impulsivity predicted the drug’s effect in poly-SUD.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/30402987/.
Sherman MM, Ungureanu S, Rey JA. Naltrexone/Bupropion ER (Contrave): Newly Approved Treatment Option for Chronic Weight Management in Obese Adults. P T. 2016 Mar;41(3):164-72. PMID: 26957883; PMCID: PMC4771085.
Naltrexone/Bupropion ER (Contrave): Newly Approved Treatment Option for Chronic Weight Management in Obese Adults
Naltrexone/bupropion ER (Contrave): newly approved treatment option for chronic weight management in obese adults.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/26957883/.
Patten DK, Schultz BG, Berlau DJ. The Safety and Efficacy of Low-Dose Naltrexone in the Management of Chronic Pain and Inflammation in Multiple Sclerosis, Fibromyalgia, Crohn’s Disease, and Other Chronic Pain Disorders. Pharmacotherapy. 2018 Mar;38(3):382-389. doi: 10.1002/phar.2086. Epub 2018 Feb 23. PMID: 29377216.
The Safety and Efficacy of Low-Dose Naltrexone in the Management of Chronic Pain and Inflammation in Multiple Sclerosis, Fibromyalgia, Crohn’s Disease, and Other Chronic Pain Disorders
Low-dose naltrexone (LDN) is used off-label to treat pain and inflammation in conditions like multiple sclerosis, Crohn’s disease, and fibromyalgia, though it is primarily approved for opioid and alcohol dependence. While evidence supports its safety and tolerability, its efficacy remains less clear, with benefits mainly seen in subjective measures like pain relief and quality of life. More research is needed to confirm its effectiveness in these conditions.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/29377216/.
Marcus NJ, Robbins L, Araki A, Gracely EJ, Theoharides TC. Effective Doses of Low-Dose Naltrexone for Chronic Pain – An Observational Study. J Pain Res. 2024 Mar 21;17:1273-1284. doi: 10.2147/JPR.S451183. PMID: 38532991; PMCID: PMC10964028.
Effective Doses of Low-Dose Naltrexone for Chronic Pain – An Observational Study
Low-dose naltrexone (LDN) shows potential for treating chronic nociplastic pain, with effective doses varying between 0.1 and 4.5 mg per day. An observational study of 41 patients found that titrating LDN to a personalized dose significantly improved pain and other symptoms, highlighting the need for individualized dosing strategies.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/38532991/.
McKenzie-Brown AM, Boorman DW, Ibanez KR, Agwu E, Singh V. Low-Dose Naltrexone (LDN) for Chronic Pain at a Single Institution: A Case Series. J Pain Res. 2023 Jun 14;16:1993-1998. doi: 10.2147/JPR.S389957. PMID: 37337611; PMCID: PMC10276990.
Low-Dose Naltrexone (LDN) for Chronic Pain at a Single Institution: A Case Series
Low-dose naltrexone (LDN) shows promise in reducing chronic pain, particularly in patients with neuropathic pain and complex regional pain syndrome (CRPS), where 64% of users experienced relief. However, patients with spondylosis were significantly less likely to respond. A trial of several weeks may be necessary to assess LDN’s analgesic effects.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/37337611/.
Kim PS, Fishman MA. Low-Dose Naltrexone for Chronic Pain: Update and Systemic Review. Curr Pain Headache Rep. 2020 Aug 26;24(10):64. doi: 10.1007/s11916-020-00898-0. PMID: 32845365.
Low-Dose Naltrexone for Chronic Pain: Update and Systemic Review
This review examines the potential of low-dose naltrexone (LDN) for treating chronic pain, highlighting its promise in conditions like fibromyalgia and multiple sclerosis through modulation of neuroinflammation and glial cell activity. Further clinical investigation is recommended due to its unique effects at low doses.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/32845365/.
Poliwoda S, Noss B, Truong GTD, Creech ZA, Koushik SS, Urits I, Viswanath O. The Utilization of Low Dose Naltrexone for Chronic Pain. CNS Drugs. 2023 Aug;37(8):663-670. doi: 10.1007/s40263-023-01018-3. Epub 2023 Jul 28. PMID: 37505425.
The Utilization of Low Dose Naltrexone for Chronic Pain
Naltrexone, a mu-opioid receptor antagonist, is used to reverse opioid toxicity and prevent relapse by reducing cravings and withdrawal symptoms. It is also approved for alcohol abuse and has shown promise in treating chronic pain conditions like fibromyalgia, multiple sclerosis, and inflammatory bowel disease, though more studies are needed for approval in chronic pain management.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/37505425/.
Driver CN, D’Souza RS. Efficacy of Low-Dose Naltrexone and Predictors of Treatment Success or Discontinuation in Fibromyalgia and Other Chronic Pain Conditions: A Fourteen-Year, Enterprise-Wide Retrospective Analysis. Biomedicines. 2023 Apr 3;11(4):1087. doi: 10.3390/biomedicines11041087. PMID: 37189705; PMCID: PMC10135963.
Efficacy of Low-Dose Naltrexone and Predictors of Treatment Success or Discontinuation in Fibromyalgia and Other Chronic Pain Conditions: A Fourteen-Year, Enterprise-Wide Retrospective Analysis. Biomedicines
Low-dose naltrexone (LDN) is a potential treatment for chronic pain, including fibromyalgia, with 65% of patients reporting pain relief. In a study of 115 patients, LDN was generally well-tolerated, though 36% discontinued use and 11% reported side effects. Further research is needed to better understand its efficacy.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/37189705/.
Metyas S, Chen CL, Yeter K, Solyman J, Arkfeld DG. Low Dose Naltrexone in the Treatment of Fibromyalgia. Curr Rheumatol Rev. 2018;14(2):177-180. doi: 10.2174/1573397113666170321120329. PMID: 28325149.
Low Dose Naltrexone in the Treatment of Fibromyalgia. Curr Rheumatol Rev
Low-dose naltrexone (LDN) shows promise as a safe, effective, and affordable treatment for fibromyalgia, potentially alleviating pain by enhancing endorphin function, though larger controlled trials are needed to confirm these findings.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/28325149/.
N Irwin M, A Cooke D, Berland D, D Marshall V, A Smith M. Efficacy and Safety of Low Dose Naltrexone for Chronic Pain. J Pain Palliat Care Pharmacother. 2024 Mar;38(1):13-19. doi: 10.1080/15360288.2024.2302550. Epub 2024 Feb 1. PMID: 38301136.
Efficacy and Safety of Low Dose Naltrexone for Chronic Pain
A retrospective study at a pain clinic found that low-dose naltrexone (LDN) significantly reduced Pain, Enjoyment of Life, and General Activity (PEG) scores in chronic pain patients, but over 75% discontinued due to lack of benefit, with 23% experiencing side effects.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/38301136/.
Jackson D, Singh S, Zhang-James Y, Faraone S, Johnson B. The Effects of Low Dose Naltrexone on Opioid Induced Hyperalgesia and Fibromyalgia. Front Psychiatry. 2021 Feb 16;12:593842. doi: 10.3389/fpsyt.2021.593842. PMID: 33664680; PMCID: PMC7921161.
The Effects of Low Dose Naltrexone on Opioid Induced Hyperalgesia and Fibromyalgia
The study aimed to assess the impact of chronic opioid treatment on pain tolerance, specifically looking at opioid-induced hyperalgesia (OIH) using the cold pressor test (CPT). It involved 55 patients with OIH and 21 with fibromyalgia, who were treated with low-dose naltrexone (LDN) after detoxification. Results showed significant increases in pain tolerance—over fourfold for OIH patients and double for fibromyalgia patients—suggesting that LDN could effectively address both conditions. However, the lack of a randomized control group limited the findings.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/33664680/.
Yang J, Shin KM, Do A, Bierle DM, Abu Dabrh AM, Yin Z, Bauer BA, Mohabbat AB. The Safety and Efficacy of Low-Dose Naltrexone in Patients with Fibromyalgia: A Systematic Review. J Pain Res. 2023 Mar 21;16:1017-1023. doi: 10.2147/JPR.S395457. PMID: 36974308; PMCID: PMC10039621.
The Safety and Efficacy of Low-Dose Naltrexone in Patients with Fibromyalgia: A Systematic Review
Fibromyalgia (FM) is a chronic pain syndrome marked by widespread musculoskeletal pain, and low-dose naltrexone (LDN) is increasingly used off-label for treatment. A systematic review of the literature identified nine studies on LDN’s safety and efficacy in FM, revealing that LDN may effectively manage symptoms with no severe adverse events reported. However, the current evidence is limited and calls for more rigorous trials with larger samples to better establish its efficacy and safety.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/36974308/.
Goel A, Kapoor B, Wu M, Iyayi M, Englesakis M, Kohan L, Ladha KS, Clarke HA. Perioperative Naltrexone Management: A Scoping Review by the Perioperative Pain and Addiction Interdisciplinary Network. Anesthesiology. 2024 Aug 1;141(2):388-399. doi: 10.1097/ALN.0000000000005040. PMID: 38980158.
Perioperative Naltrexone Management: A Scoping Review by the Perioperative Pain and Addiction Interdisciplinary Network
This review highlights the inconsistent and controversial perioperative management of patients on naltrexone, commonly prescribed for substance use and chronic pain disorders. A systematic review identified limited and low-quality evidence, with guidelines mostly recommending preoperative cessation of naltrexone without considering patient recovery from substance use. Future research should address both pain management and relapse prevention in these patients.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/38980158/.
Anton RF. Naltrexone for the management of alcohol dependence. N Engl J Med. 2008 Aug 14;359(7):715-21. doi: 10.1056/NEJMct0801733. PMID: 18703474; PMCID: PMC2565602.
Naltrexone for the management of alcohol dependence
A 44-year-old businessman with hypertension, stress, poor sleep, and elevated liver enzymes admits to excessive alcohol consumption. Despite no depression, he wonders about cutting down on drinking. His physician proposes naltrexone or referral to an alcohol clinic for further evaluation.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/18703474/.
Pettinati HM, O’Brien CP, Rabinowitz AR, Wortman SP, Oslin DW, Kampman KM, Dackis CA. The status of naltrexone in the treatment of alcohol dependence: specific effects on heavy drinking. J Clin Psychopharmacol. 2006 Dec;26(6):610-25. doi: 10.1097/01.jcp.0000245566.52401.20. PMID: 17110818.
The status of naltrexone in the treatment of alcohol dependence: specific effects on heavy drinking
In a 12-week trial, alcohol-dependent patients treated with 50 mg/day of naltrexone reported significantly less alcohol craving and relapse compared to a placebo group. Only 23% of naltrexone-treated patients relapsed versus 54.3% of the placebo group, with the greatest effect seen in those who drank while in outpatient treatment. Naltrexone had minimal side effects and did not affect mood or psychiatric symptoms.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/1345133/.
Krystal JH, Cramer JA, Krol WF, Kirk GF, Rosenheck RA; Veterans Affairs Naltrexone Cooperative Study 425 Group. Naltrexone in the treatment of alcohol dependence. N Engl J Med. 2001 Dec 13;345(24):1734-9. doi: 10.1056/NEJMoa011127. PMID: 11742047.
Naltrexone in the treatment of alcohol dependence
A year-long study on 627 veterans with severe alcohol dependence found no significant benefit of naltrexone compared to placebo in preventing relapse or reducing drinking. These results do not support naltrexone’s efficacy for treating chronic alcohol dependence in men.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/11742047/.
Morris PL, Hopwood M, Whelan G, Gardiner J, Drummond E. Naltrexone for alcohol dependence: a randomized controlled trial. Addiction. 2001 Nov;96(11):1565-73. doi: 10.1046/j.1360-0443.2001.961115654.x. PMID: 11784454.
Naltrexone for alcohol dependence: a randomized controlled trial
This study examined the efficacy of naltrexone in treating alcohol dependence in men through a 12-week trial. Participants who took naltrexone had fewer relapses compared to those on a placebo, and those who completed the trial consumed less alcohol. Naltrexone was well-tolerated, suggesting its effectiveness in preventing relapse with minimal psychosocial support.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/11784454/.
Garbutt JC. Efficacy and tolerability of naltrexone in the management of alcohol dependence. Curr Pharm Des. 2010;16(19):2091-7. doi: 10.2174/138161210791516459. PMID: 20482515.
Efficacy and tolerability of naltrexone in the management of alcohol dependence
Naltrexone, an opioid-receptor antagonist, has been shown to modestly reduce heavy drinking relapse in alcohol dependence, though its effect on abstinence is less pronounced. It is generally well-tolerated, with nausea as a common side effect, and hepatotoxicity being a concern only at higher doses. Intramuscular versions have proven effective, and ongoing research aims to refine its role in treatment.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/20482515/.
Kranzler HR, Modesto-Lowe V, Van Kirk J. Naltrexone vs. nefazodone for treatment of alcohol dependence. A placebo-controlled trial. Neuropsychopharmacology. 2000 May;22(5):493-503. doi: 10.1016/S0893-133X(99)00135-9. PMID: 10731624.
Naltrexone vs. nefazodone for treatment of alcohol dependence
This study found that nefazodone is not effective for treating alcohol dependence, and while naltrexone caused more adverse effects and lower treatment compliance, neither medication showed significant differences in reducing drinking behavior compared to a placebo.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/10731624/.
Palpacuer C, Duprez R, Huneau A, Locher C, Boussageon R, Laviolle B, Naudet F. Pharmacologically controlled drinking in the treatment of alcohol dependence or alcohol use disorders: a systematic review with direct and network meta-analyses on nalmefene, naltrexone, acamprosate, baclofen and topiramate. Addiction. 2018 Feb;113(2):220-237. doi: 10.1111/add.13974. Epub 2017 Sep 20. PMID: 28940866.
Pharmacologically controlled drinking in the treatment of alcohol dependence or alcohol use disorders: a systematic review with direct and network meta-analyses on nalmefene, naltrexone, acamprosate, baclofen and topiramate. Addiction
This systematic review and meta-analysis assessed the effectiveness of nalmefene, naltrexone, acamprosate, baclofen, and topiramate in controlling drinking in patients with alcohol dependence or alcohol use disorders. While nalmefene, baclofen, and topiramate showed some efficacy in reducing alcohol consumption, naltrexone and acamprosate did not. However, none of the treatments showed clear benefits on health outcomes, and all studies had a high risk of bias.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/28940866/.
Kranzler HR, Van Kirk J. Efficacy of naltrexone and acamprosate for alcoholism treatment: a meta-analysis. Alcohol Clin Exp Res. 2001 Sep;25(9):1335-41. PMID: 11584154.
Efficacy of naltrexone and acamprosate for alcoholism treatment: a meta-analysis
A meta-analysis of placebo-controlled trials found that both naltrexone and acamprosate are effective in reducing alcohol consumption in alcohol dependence, showing significant but modest effects on treatment retention and drinking outcomes, with no clear difference in their efficacy. In contrast, selective serotonin reuptake inhibitors demonstrated consistently greater effects on depressive symptoms. The study highlights the need for clearer roles for these medications in treatment and suggests further development of pharmacotherapy for alcoholism.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/11584154/.
Center for Substance Abuse Treatment. Naltrexone and Alcoholism Treatment. Rockville (MD): Substance Abuse and Mental Health Services Administration (US); 1998. Report No.: (SMA) 98-3206. PMID: 22514834.
Naltrexone and Alcoholism Treatment
In a 12-week, double-blind, placebo-controlled trial, 70 male alcohol-dependent patients receiving naltrexone hydrochloride (50 mg/d) experienced significantly reduced alcohol cravings and relapse rates compared to those on placebo, with only 23% of naltrexone users relapsing versus 54.3% of placebo users. Naltrexone’s efficacy was particularly notable among those who consumed alcohol during outpatient treatment, with significantly fewer relapses following alcohol exposure. The treatment had minimal side effects and did not cause mood changes, indicating that naltrexone may be a safe and effective adjunct therapy for preventing alcohol relapse.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/1345133/.
Krupitsky E, Zvartau E, Woody G. Use of naltrexone to treat opioid addiction in a country in which methadone and buprenorphine are not available. Curr Psychiatry Rep. 2010 Oct;12(5):448-53. doi: 10.1007/s11920-010-0135-5. PMID: 20640538; PMCID: PMC3160743.
Use of naltrexone to treat opioid addiction in a country in which methadone and buprenorphine are not available
Naltrexone is a medication that effectively blocks the effects of opioids and helps prevent relapse in detoxified opioid addicts, but poor compliance is a major challenge, especially in countries where substitution therapies are not permitted. In Russia, where substitution therapy is illegal, naltrexone is the sole pharmacotherapy for heroin dependence, and due to stronger family support for adherence, it proves more effective for relapse prevention compared to Western countries. Long-acting formulations, such as injectables and implants, are particularly beneficial, as highlighted by recent studies conducted in Russia.
You can read the abstract of this article at
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3160743/.
Sullivan MA, Bisaga A, Mariani JJ, Glass A, Levin FR, Comer SD, Nunes EV. Naltrexone treatment for opioid dependence: does its effectiveness depend on testing the blockade? Drug Alcohol Depend. 2013 Nov 1;133(1):80-5. doi: 10.1016/j.drugalcdep.2013.05.030. Epub 2013 Jul 1. PMID: 23827259; PMCID: PMC3955093.
Naltrexone treatment for opioid dependence: does its effectiveness depend on testing the blockade?
A study on the efficacy of long-acting injectable naltrexone (Vivitrol) for opioid dependence found that opiate-positive urine tests predicted dropout in placebo and low-dose groups, but not in the high-dose group, where such tests correlated with sustained abstinence. Retention was higher in both naltrexone groups among patients without opiate-positive tests, suggesting that naltrexone not only helps extinguish drug-seeking behavior but may also reduce cravings and normalize neuroendocrine systems, emphasizing the importance of dosage for effective treatment.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/23827259/.
Rigg KK. Attitudes toward extended-release naltrexone treatment for opioid use disorder among African Americans. Drug Alcohol Depend. 2024 Apr 1;257:111260. doi: 10.1016/j.drugalcdep.2024.111260. Epub 2024 Mar 8. PMID: 38492256.
Attitudes toward extended-release naltrexone treatment for opioid use disorder among African Americans
A study examining attitudes toward extended-release naltrexone (XR-NTX) among African American adults with opioid use disorder found generally positive perceptions of the medication, particularly its non-addictive nature, monthly injection convenience, and perceived effectiveness compared to other treatments. This research highlights a potentially favorable view of XR-NTX among this demographic, contributing valuable insights to the understanding of opioid treatment preferences.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/38492256/.
Cornish JW, Metzger D, Woody GE, Wilson D, McLellan AT, Vandergrift B, O’Brien CP. Naltrexone pharmacotherapy for opioid dependent federal probationers. J Subst Abuse Treat. 1997 Nov-Dec;14(6):529-34. doi: 10.1016/s0740-5472(97)00020-2. PMID: 9437624.
Naltrexone pharmacotherapy for opioid dependent federal probationers
A study involving federal probationers or parolees with opioid addiction examined the effects of naltrexone combined with brief drug counseling compared to counseling alone. Out of 51 participants, 52% in the naltrexone group completed the 6-month program, showing significantly lower opioid use (8% positive urine tests) compared to 30% in the control group. Additionally, fewer participants in the naltrexone group (26%) had their probation revoked compared to the controls (56%), indicating that integrating naltrexone treatment into the probation system can improve outcomes related to opioid use and recidivism.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/9437624/.
Shulman M, Greiner MG, Tafessu HM, Opara O, Ohrtman K, Potter K, Hefner K, Jelstrom E, Rosenthal RN, Wenzel K, Fishman M, Rotrosen J, Ghitza UE, Nunes EV, Bisaga A. Rapid Initiation of Injection Naltrexone for Opioid Use Disorder: A Stepped-Wedge Cluster Randomized Clinical Trial. JAMA Netw Open. 2024 May 1;7(5):e249744. doi: 10.1001/jamanetworkopen.2024.9744. PMID: 38717773; PMCID: PMC11079685.
Rapid Initiation of Injection Naltrexone for Opioid Use Disorder: A Stepped-Wedge Cluster Randomized Clinical Trial
A study compared the effectiveness of rapid versus standard procedures for initiating injectable extended-release (XR) naltrexone in patients with opioid use disorder (OUD). Conducted at six community addiction treatment units, the rapid procedure, which involved a shorter buprenorphine taper and quicker transition to XR-naltrexone, resulted in successful initiation rates of 62.7%, compared to 35.8% with the standard procedure. While the rapid approach required more intensive monitoring, it demonstrated noninferiority to the standard method and could enhance the accessibility of XR-naltrexone as a treatment option for OUD.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/38717773/.
Jarvis BP, Holtyn AF, Subramaniam S, Tompkins DA, Oga EA, Bigelow GE, Silverman K. Extended-release injectable naltrexone for opioid use disorder: a systematic review. Addiction. 2018 Jul;113(7):1188-1209. doi: 10.1111/add.14180. Epub 2018 Mar 24. PMID: 29396985; PMCID: PMC5993595.
Extended-release injectable naltrexone for opioid use disorder: a systematic review
This systematic review examines the effectiveness of extended-release naltrexone (XR-NTX) for treating opioid use disorder by analyzing 34 studies from 2006 to 2017. Findings indicate that induction success is higher in individuals already detoxified (85%) versus those needing detoxification (62.6%). Adherence rates to XR-NTX are low, with only 44.2% completing scheduled injections, though adherence is better in research studies compared to routine care. XR-NTX reduces opioid use compared to placebo, particularly in criminal justice settings, but shows limited clinical utility due to high dropout rates and few experimental validations of its efficacy.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/29396985/.
Larney S, Gowing L, Mattick RP, Farrell M, Hall W, Degenhardt L. A systematic review and meta-analysis of naltrexone implants for the treatment of opioid dependence. Drug Alcohol Rev. 2014 Mar;33(2):115-28. doi: 10.1111/dar.12095. Epub 2013 Dec 3. PMID: 24299657.
A systematic review and meta-analysis of naltrexone implants for the treatment of opioid dependence
A systematic review assessed the safety and efficacy of naltrexone implants for opioid dependence, analyzing five randomized trials and four non-randomized studies. Results indicated that naltrexone implants were more effective than placebo and oral naltrexone in suppressing opioid use, but showed no significant difference compared to methadone maintenance, based on low-quality evidence. The overall quality of evidence was moderate to very low, highlighting the need for better-designed research before naltrexone implants can be widely recommended for treatment outside clinical trials.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/24299657/.
Jones HE, Chisolm MS, Jansson LM, Terplan M. Naltrexone in the treatment of opioid-dependent pregnant women: the case for a considered and measured approach to research. Addiction. 2013 Feb;108(2):233-47. doi: 10.1111/j.1360-0443.2012.03811.x. Epub 2012 Apr 4. PMID: 22471668.
Naltrexone in the treatment of opioid-dependent pregnant women: the case for a considered and measured approach to research
The paper reviews the use of naltrexone for treating opioid dependence during pregnancy, highlighting its potential benefits such as blocking euphoric effects and a favorable side effect profile, while also noting significant risks like induction challenges, relapse, and overdose. It calls for careful evaluation of the benefits and risks for mothers and their children, alongside a commitment to ethical research to improve outcomes for those affected by opioid dependence.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/22471668/.
Mitchell SG, Monico LB, Gryczynski J, Fishman MJ, O’Grady KE, Schwartz RP. Extended-release naltrexone for youth with opioid use disorder. J Subst Abuse Treat. 2021 Nov;130:108407. doi: 10.1016/j.jsat.2021.108407. Epub 2021 Apr 15. PMID: 34118699; PMCID: PMC8478707.
Extended-release naltrexone for youth with opioid use disorder
A randomized controlled trial involving 288 adolescents and young adults (ages 15-21) with moderate to severe opioid use disorder (OUD) evaluated the effectiveness of extended-release naltrexone (XR-NTX) compared to treatment-as-usual (TAU). Due to significant participant nonadherence, results showed no significant differences in self-reported substance use between groups in intention-to-treat analyses. However, those receiving XR-NTX reported less opioid use over 90 days, highlighting the need for treatment programs to consider XR-NTX for motivated youth and for future research to improve adherence strategies.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/34118699/.
Sudakin D. Naltrexone: Not Just for Opioids Anymore. J Med Toxicol. 2016 Mar;12(1):71-5. doi: 10.1007/s13181-015-0512-x. PMID: 26546222; PMCID: PMC4781804.
Naltrexone: Not Just for Opioids Anymore
Naltrexone, a semi-synthetic opioid antagonist effective for alcohol and opioid dependence, faces adherence challenges in daily dosing; however, a recently FDA-approved long-acting injectable formulation offers a promising solution. This article reviews its pharmacology, evidence for extended-release use, and clinical challenges in patient induction.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/26546222/.
Cousins SJ, Radfar SR, Crèvecoeur-MacPhail D, Ang A, Darfler K, Rawson RA. Predictors of Continued Use of Extended-Released Naltrexone (XR-NTX) for Opioid-Dependence: An Analysis of Heroin and Non-Heroin Opioid Users in Los Angeles County. J Subst Abuse Treat. 2016 Apr;63:66-71. doi: 10.1016/j.jsat.2015.12.004. Epub 2015 Dec 29. PMID: 26823295.
Predictors of Continued Use of Extended-Released Naltrexone (XR-NTX) for Opioid-Dependence: An Analysis of Heroin and Non-Heroin Opioid Users in Los Angeles County
Extended-release naltrexone (XR-NTX) is linked to more opioid-free days, better adherence in substance use disorder treatments, and reduced cravings, but its utilization among opioid-dependent patients based on baseline characteristics is not well understood. The study found that XR-NTX effectively decreases urges to use opioids in both heroin and non-heroin users, with similar retention rates in treatment. However, retention was lower for individuals who were homeless, injected opioids, or had a mental illness.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/26823295/
Tanum L, Solli KK, Latif ZE, Benth JŠ, Opheim A, Sharma-Haase K, Krajci P, Kunøe N. Effectiveness of Injectable Extended-Release Naltrexone vs Daily Buprenorphine-Naloxone for Opioid Dependence: A Randomized Clinical Noninferiority Trial. JAMA Psychiatry. 2017 Dec 1;74(12):1197-1205. doi: 10.1001/jamapsychiatry.2017.3206. Erratum in: JAMA Psychiatry. 2018 Mar 14;75(5):530. doi: 10.1001/jamapsychiatry.2018.0238. PMID: 29049469; PMCID: PMC6583381.
Effectiveness of Injectable Extended-Release Naltrexone vs Daily Buprenorphine-Naloxone for Opioid Dependence: A Randomized Clinical Noninferiority Trial
A clinical trial comparing extended-release naltrexone hydrochloride and buprenorphine-naloxone in treating opioid dependence found that naltrexone was as effective as buprenorphine-naloxone in maintaining short-term abstinence from heroin and other illicit substances in newly detoxified individuals. The study, conducted in Norway with 232 participants, showed similar retention rates and opioid-negative urine test results, supporting naltrexone as a viable treatment option for opioid dependence.
You can read the abstract of this article at
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6583381/.
Morgan JR, Schackman BR, Leff JA, Linas BP, Walley AY. Injectable naltrexone, oral naltrexone, and buprenorphine utilization and discontinuation among individuals treated for opioid use disorder in a United States commercially insured population. J Subst Abuse Treat. 2018 Feb;85:90-96. doi: 10.1016/j.jsat.2017.07.001. Epub 2017 Jul 3. PMID: 28733097; PMCID: PMC5750108.
Injectable naltrexone, oral naltrexone, and buprenorphine utilization and discontinuation among individuals treated for opioid use disorder in a United States commercially insured population
This study examined the prescribing patterns for four medications for opioid use disorder (OUD) in a claims-based database from 2010 to 2014, revealing a fourfold increase in OUD diagnoses while the proportion of patients receiving medication decreased from 25% to 16%. Discontinuation rates after 30 days of treatment were notably high across all medication types, particularly for injectable and oral naltrexone. The findings highlight a gap between the rising incidence of OUD and the adoption of effective treatments, emphasizing the need for enhanced strategies to improve medication access and adherence amid the opioid crisis.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/28733097/.
Hartung DM, McCarty D, Fu R, Wiest K, Chalk M, Gastfriend DR. Extended-release naltrexone for alcohol and opioid dependence: a meta-analysis of healthcare utilization studies. J Subst Abuse Treat. 2014 Aug;47(2):113-21. doi: 10.1016/j.jsat.2014.03.007. Epub 2014 Apr 13. PMID: 24854219; PMCID: PMC4110954.
Extended-release naltrexone for alcohol and opioid dependence: a meta-analysis of healthcare utilization studies
This study compared the cost and healthcare utilization outcomes of once-monthly injectable extended-release naltrexone (XR-NTX) to other approved treatments for alcohol and opioid dependence. It found that alcohol-dependent patients using XR-NTX had better medication refill persistence compared to acamprosate and oral naltrexone, and generally incurred similar or lower healthcare costs. Opioid-dependent patients on XR-NTX had lower inpatient substance abuse-related utilization and significantly reduced total costs compared to methadone.
For further reading, you may explore studies on the effectiveness of XR-NTX in long-term addiction management or research on cost-effectiveness in substance use disorder treatments.
You can read the abstract of this article at
https://pubmed.ncbi.nlm.nih.gov/24854219/.
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