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Risk of Suicide and Psychiatric Disorders Among Isotretinoin Users: A Meta-Analysis
IMPORTANCE: Isotretinoin is hypothesized to contribute to the development of psychiatric disorders, but the epidemiological association and risk factors associated with psychiatric disorders among isotretinoin users remain unclear. OBJECTIVE: To clarify the absolute and relative risk and risk factor...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Medical Association
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10687715/ https://www.ncbi.nlm.nih.gov/pubmed/38019562 http://dx.doi.org/10.1001/jamadermatol.2023.4579 |
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author | Tan, Nicole Kye Wen Tang, Adelina MacAlevey, Neil Chen Yi Lun Tan, Benjamin Kye Jyn Oon, Hazel H. |
author_facet | Tan, Nicole Kye Wen Tang, Adelina MacAlevey, Neil Chen Yi Lun Tan, Benjamin Kye Jyn Oon, Hazel H. |
author_sort | Tan, Nicole Kye Wen |
collection | PubMed |
description | IMPORTANCE: Isotretinoin is hypothesized to contribute to the development of psychiatric disorders, but the epidemiological association and risk factors associated with psychiatric disorders among isotretinoin users remain unclear. OBJECTIVE: To clarify the absolute and relative risk and risk factors associated with suicide and psychiatric disorders among isotretinoin users. DATA SOURCES: PubMed, Embase, Web of Science, and Scopus were searched from inception until January 24, 2023. STUDY SELECTION: Randomized trials and observational studies were selected if they reported the absolute risk, relative risk, and risk factors for suicide and psychiatric disorders among isotretinoin users. DATA EXTRACTION AND SYNTHESIS: Relevant data were extracted and risk of bias was evaluated at the study level using the Newcastle-Ottawa Scale. Data were pooled using inverse variance-weighted meta-analyses. Heterogeneity was measured using the I(2) statistic, and meta-regression analyses were performed. MAIN OUTCOMES AND MEASURES: Absolute risk (percentage), relative risks (risk ratios [RR]), and risk factors (RR) of suicide and psychiatric disorders among isotretinoin users. RESULTS: A total of 25 studies including 1 625 891 participants were included in the review and 24 in the meta-analysis. Among the included studies, participants’ average age ranged from 16 to 38 years, and distribution by sex ranged from 0% to 100% male. The 1-year pooled absolute risk from between 2 and 8 studies of completed suicide, suicide attempt, suicide ideation, and self-harm were each less than 0.5%, while that of depression was 3.83% (95% CI, 2.45-5.93; I(2) = 77%) in 11 studies. Isotretinoin users were less likely than nonusers to attempt suicide at 2 years (RR, 0.92; 95% CI, 0.84-1.00; I(2) = 0%), 3 years (RR, 0.86; 95% CI, 0.77-0.95; I(2) = 0%), and 4 years (RR, 0.85; 95% CI, 0.72-1.00; I(2) = 23%) following treatment. Isotretinoin was not associated with the risk of all psychiatric disorders (RR, 1.08; 95% CI, 0.99-1.19; I(2) = 0%). Study-level meta-regression found that studies with participants of older age reported lower 1-year absolute risk of depression, while those with a higher percentage of male participants reported a higher 1-year absolute risk of completed suicide. CONCLUSIONS AND RELEVANCE: The findings suggest that at a population level, isotretinoin users do not have increased risk of suicide or psychiatric conditions but may instead have a lower risk of suicide attempts at 2 to 4 years following treatment. While these findings are reassuring, clinicians should continue to practice holistic psychodermatologic care and monitor patients for signs of mental distress during isotretinoin treatment. |
format | Online Article Text |
id | pubmed-10687715 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Medical Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-106877152023-12-01 Risk of Suicide and Psychiatric Disorders Among Isotretinoin Users: A Meta-Analysis Tan, Nicole Kye Wen Tang, Adelina MacAlevey, Neil Chen Yi Lun Tan, Benjamin Kye Jyn Oon, Hazel H. JAMA Dermatol Original Investigation IMPORTANCE: Isotretinoin is hypothesized to contribute to the development of psychiatric disorders, but the epidemiological association and risk factors associated with psychiatric disorders among isotretinoin users remain unclear. OBJECTIVE: To clarify the absolute and relative risk and risk factors associated with suicide and psychiatric disorders among isotretinoin users. DATA SOURCES: PubMed, Embase, Web of Science, and Scopus were searched from inception until January 24, 2023. STUDY SELECTION: Randomized trials and observational studies were selected if they reported the absolute risk, relative risk, and risk factors for suicide and psychiatric disorders among isotretinoin users. DATA EXTRACTION AND SYNTHESIS: Relevant data were extracted and risk of bias was evaluated at the study level using the Newcastle-Ottawa Scale. Data were pooled using inverse variance-weighted meta-analyses. Heterogeneity was measured using the I(2) statistic, and meta-regression analyses were performed. MAIN OUTCOMES AND MEASURES: Absolute risk (percentage), relative risks (risk ratios [RR]), and risk factors (RR) of suicide and psychiatric disorders among isotretinoin users. RESULTS: A total of 25 studies including 1 625 891 participants were included in the review and 24 in the meta-analysis. Among the included studies, participants’ average age ranged from 16 to 38 years, and distribution by sex ranged from 0% to 100% male. The 1-year pooled absolute risk from between 2 and 8 studies of completed suicide, suicide attempt, suicide ideation, and self-harm were each less than 0.5%, while that of depression was 3.83% (95% CI, 2.45-5.93; I(2) = 77%) in 11 studies. Isotretinoin users were less likely than nonusers to attempt suicide at 2 years (RR, 0.92; 95% CI, 0.84-1.00; I(2) = 0%), 3 years (RR, 0.86; 95% CI, 0.77-0.95; I(2) = 0%), and 4 years (RR, 0.85; 95% CI, 0.72-1.00; I(2) = 23%) following treatment. Isotretinoin was not associated with the risk of all psychiatric disorders (RR, 1.08; 95% CI, 0.99-1.19; I(2) = 0%). Study-level meta-regression found that studies with participants of older age reported lower 1-year absolute risk of depression, while those with a higher percentage of male participants reported a higher 1-year absolute risk of completed suicide. CONCLUSIONS AND RELEVANCE: The findings suggest that at a population level, isotretinoin users do not have increased risk of suicide or psychiatric conditions but may instead have a lower risk of suicide attempts at 2 to 4 years following treatment. While these findings are reassuring, clinicians should continue to practice holistic psychodermatologic care and monitor patients for signs of mental distress during isotretinoin treatment. American Medical Association 2023-11-29 /pmc/articles/PMC10687715/ /pubmed/38019562 http://dx.doi.org/10.1001/jamadermatol.2023.4579 Text en Copyright 2023 Tan NKW et al. JAMA Dermatology. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the CC-BY License. |
spellingShingle | Original Investigation Tan, Nicole Kye Wen Tang, Adelina MacAlevey, Neil Chen Yi Lun Tan, Benjamin Kye Jyn Oon, Hazel H. Risk of Suicide and Psychiatric Disorders Among Isotretinoin Users: A Meta-Analysis |
title | Risk of Suicide and Psychiatric Disorders Among Isotretinoin Users: A Meta-Analysis |
title_full | Risk of Suicide and Psychiatric Disorders Among Isotretinoin Users: A Meta-Analysis |
title_fullStr | Risk of Suicide and Psychiatric Disorders Among Isotretinoin Users: A Meta-Analysis |
title_full_unstemmed | Risk of Suicide and Psychiatric Disorders Among Isotretinoin Users: A Meta-Analysis |
title_short | Risk of Suicide and Psychiatric Disorders Among Isotretinoin Users: A Meta-Analysis |
title_sort | risk of suicide and psychiatric disorders among isotretinoin users: a meta-analysis |
topic | Original Investigation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10687715/ https://www.ncbi.nlm.nih.gov/pubmed/38019562 http://dx.doi.org/10.1001/jamadermatol.2023.4579 |
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