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Utility of Naltrexone Treatment for Chronic Inflammatory Dermatologic Conditions: A Systematic Review
Chloe Ekelem1, Margit Juhasz1, Pooja Khera2
1Department of Dermatology, University of California, Irvine.
Importance:
Dermatology is encountering increasing rates of autoimmune disease manifesting in primary skin conditions that are difficult to treat without a risk of immunosuppression. Naltrexone is an orally active opioid antagonist that influences a variety of systemic pathways, including the immune system, in low doses of 1.5 to 4.0 mg/d. This phenomenon has piqued the interest of researchers and practitioners in regard to low-dose naltrexone's potential in the treatment of several autoimmune conditions.
Objective:
To review the existing literature on naltrexone treatment for dermatologic conditions.
Evidence Review:
A primary literature search was conducted using PubMed in April 2018 for all articles published from 1971 to April 2018. Search terms consisted of naltrexone or low dose naltrexone or low-dose naltrexone and dermatology or skin or hair or nails. Reviews, animal studies, and nondermatologic and pharmacologic studies were excluded.
Findings:
From 1037 articles, 22 were deemed to be appropriate for inclusion in this review for a qualitative synthesis. The 22 articles included randomized clinical trials, case reports, and series. There were 7 articles on low-dose naltexone, 1 on topical naltrexone, and 14 on high-dose naltrexone use in dermatology. In high, low, and topical doses, naltrexone was effective in treating pruritus attributable to atopic dermatitis, prurigo nodularis, cholestatsis, burn injury, systemic sclerosis, Hailey-Hailey disease, and lichen planopilaris. High-dose naltrexone was ineffective in treating flushing and uremic pruritus most likely because of the lack of opioid involvement in the pathophysiologic mechanisms of these conditions.
Conclusions And Relevance:
The findings suggest that low-dose naltrexone is safe and effective in the treatment of Hailey-Hailey disease and lichen planopilaris and both low- and high-dose naltrexone successfully treat pruritus attributable to various pathologic conditions; however, more adverse effects occurred in those taking high doses. Low-dose naltrexone has the potential for the treatment of chronic inflammatory skin conditions; however, additional evidence is needed for dosing and long-term treatment guidelines.
Insights
Low-dose naltrexone shows promise for treating autoimmune skin conditions like Hailey-Hailey disease and lichen planopilaris. It effectively manages pruritus with fewer side effects than high-dose naltrexone, though more research is needed.
Area of Science:
- Dermatology
- Immunology
- Pharmacology
Background:
- Autoimmune skin diseases are increasing, posing treatment challenges without immunosuppression.
- Low-dose naltrexone (LDN) modulates immune pathways and is explored for autoimmune conditions.
Purpose of the Study:
- To review existing literature on naltrexone's efficacy in treating dermatologic conditions.
Main Methods:
- A comprehensive literature search was conducted on PubMed from 1971 to April 2018.
- Included studies focused on naltrexone (oral or topical) for skin, hair, or nail conditions, excluding reviews and animal studies.
Main Results:
- 22 studies were reviewed, analyzing randomized trials, case reports, and series.
- Naltrexone (all doses) effectively treated pruritus in conditions like atopic dermatitis and lichen planopilaris.
- Low-dose naltrexone demonstrated safety and efficacy for Hailey-Hailey disease and lichen planopilaris.
Conclusions:
- Low-dose naltrexone is a safe and effective option for specific autoimmune skin diseases and pruritus.
- Further research is required to establish optimal dosing and long-term treatment guidelines for LDN in dermatology.
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