{"title":"Causal Link of Distinct Mental Disorders with Androgenetic Alopecia and Alopecia Areata: A Bidirectional Two-Sample Mendelian Randomization Study.","authors":"Chunyu Hu, Zhen Cheng, Yuanling Tao, Laixi Zhang, Yalan Zhang, Zongtao Chen","doi":"10.2147/CCID.S531734","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>The concern that mental states affect the hair-loss has been growing, but the causal evidence is still limited. We aimed to investigate whether and in which direction there is a causal link of distinct mental disorders with androgenetic alopecia (AGA) and alopecia areata (AA) in European population.</p><p><strong>Methods: </strong>We performed a bidirectional two-sample Mendelian randomization (MR) study to test their causality using summary statistics. The datasets of major depression disorder, anxiety disorder, panic attack, distress, and bipolar disorder were all accessed through the IEU OpenGWAS project. The datasets employed for AGA and AA analysis were sourced from the FinnGen release 10 databases, including 219,469 (220 AGA cases and 219,249 controls) and 394,872 (767 AA cases and 394,105 controls) participants, respectively. We utilized five extensively employed MR techniques to explore the bidirectional causal associations, including inverse variance weighted (IVW), weighted median, MR-Egger, weighted mode, and penalised weighted median.</p><p><strong>Results: </strong>Based on the IVW method, a bidirectional causal association was revealed whereby major depression disorder is associated with an increased risk of AA (OR: 1.59; 95% CI: 1.16-2.17) and vice versa (OR: 1.02; 95% CI: 1.00-1.03). Notably, the statistical power of MR estimates was both <80%. No association of any genetically predicted mental disorders with AGA was found. Sensitivity analyses substantiated the robustness and reliability of our findings.</p><p><strong>Conclusion: </strong>Our findings showed a bidirectional causal association between major depression disorder and AA, supporting the importance of therapies aimed at handling mental states for the prevention or treatment of AA rather than AGA.</p>","PeriodicalId":10447,"journal":{"name":"Clinical, Cosmetic and Investigational Dermatology","volume":"18 ","pages":"1727-1736"},"PeriodicalIF":2.2000,"publicationDate":"2025-07-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12262067/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical, Cosmetic and Investigational Dermatology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.2147/CCID.S531734","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"DERMATOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Background: The concern that mental states affect the hair-loss has been growing, but the causal evidence is still limited. We aimed to investigate whether and in which direction there is a causal link of distinct mental disorders with androgenetic alopecia (AGA) and alopecia areata (AA) in European population.
Methods: We performed a bidirectional two-sample Mendelian randomization (MR) study to test their causality using summary statistics. The datasets of major depression disorder, anxiety disorder, panic attack, distress, and bipolar disorder were all accessed through the IEU OpenGWAS project. The datasets employed for AGA and AA analysis were sourced from the FinnGen release 10 databases, including 219,469 (220 AGA cases and 219,249 controls) and 394,872 (767 AA cases and 394,105 controls) participants, respectively. We utilized five extensively employed MR techniques to explore the bidirectional causal associations, including inverse variance weighted (IVW), weighted median, MR-Egger, weighted mode, and penalised weighted median.
Results: Based on the IVW method, a bidirectional causal association was revealed whereby major depression disorder is associated with an increased risk of AA (OR: 1.59; 95% CI: 1.16-2.17) and vice versa (OR: 1.02; 95% CI: 1.00-1.03). Notably, the statistical power of MR estimates was both <80%. No association of any genetically predicted mental disorders with AGA was found. Sensitivity analyses substantiated the robustness and reliability of our findings.
Conclusion: Our findings showed a bidirectional causal association between major depression disorder and AA, supporting the importance of therapies aimed at handling mental states for the prevention or treatment of AA rather than AGA.
期刊介绍:
Clinical, Cosmetic and Investigational Dermatology is an international, peer-reviewed, open access journal that focuses on the latest clinical and experimental research in all aspects of skin disease and cosmetic interventions. Normal and pathological processes in skin development and aging, their modification and treatment, as well as basic research into histology of dermal and dermal structures that provide clinical insights and potential treatment options are key topics for the journal.
Patient satisfaction, preference, quality of life, compliance, persistence and their role in developing new management options to optimize outcomes for target conditions constitute major areas of interest.
The journal is characterized by the rapid reporting of clinical studies, reviews and original research in skin research and skin care.
All areas of dermatology will be covered; contributions will be welcomed from all clinicians and basic science researchers globally.