The genetics of trichotillomania and excoriation disorder: A systematic review

IF 4.3 2区 医学 Q1 PSYCHIATRY
Madison Reid , Ashley Lin , Luis C. Farhat , Thomas V. Fernandez , Emily Olfson
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引用次数: 0

Abstract

Background

Trichotillomania (TTM) and excoriation disorder (ED) are impairing obsessive-compulsive related disorders that are common in the general population and for which there are no clear first-line medications, highlighting the need to better understand the underlying biology of these disorders to inform treatments. Given the importance of genetics in obsessive-compulsive disorder (OCD), evaluating genetic factors underlying TTM and ED may advance knowledge about the pathophysiology of these body-focused repetitive behaviors.

Aim

In this systematic review, we summarize the available evidence on the genetics of TTM and ED and highlight gaps in the field warranting further research.

Method

We systematically searched Embase, PsycInfo, PubMed, Medline, Scopus, and Web of Science for original studies in genetic epidemiology (family or twin studies) and molecular genetics (candidate gene and genome-wide) published up to June 2023.

Results

Of the 3536 records identified, 109 studies were included in this review. These studies indicated that genetic factors play an important role in the development of TTM and ED, some of which may be shared across the OCD spectrum, but there are no known high-confidence specific genetic risk factors for either TTM or ED.

Conclusions

Our review underscores the need for additional genome-wide research conducted on the genetics of TTM and ED, for instance, genome-wide association and whole-genome/whole-exome DNA sequencing studies. Recent advances in genomics have led to the discovery of risk genes in several psychiatric disorders, including related conditions such as OCD, but to date, TTM and ED have remained understudied.

毛发脱落症和切除障碍的遗传学:系统回顾
背景秽语强迫症(TTM)和出汗障碍(ED)是普通人群中常见的与强迫症相关的损伤性障碍,目前尚无明确的一线治疗药物。鉴于遗传学在强迫症(OCD)中的重要性,评估TTM和ED的遗传因素可能会促进对这些以身体为中心的重复行为的病理生理学的了解。目的在这篇系统性综述中,我们总结了TTM和ED遗传学方面的现有证据,并强调了该领域中需要进一步研究的空白。方法我们系统地检索了 Embase、PsycInfo、PubMed、Medline、Scopus 和 Web of Science 中截至 2023 年 6 月发表的遗传流行病学(家族或双胞胎研究)和分子遗传学(候选基因和全基因组)方面的原始研究。这些研究表明,遗传因素在 TTM 和 ED 的发病中起着重要作用,其中一些因素可能在整个强迫症谱系中共享,但目前尚无已知的 TTM 或 ED 的高置信度特异性遗传风险因素。基因组学的最新进展发现了多种精神疾病(包括强迫症等相关疾病)的风险基因,但迄今为止,对 TTM 和 ED 的研究仍然不足。
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来源期刊
Comprehensive psychiatry
Comprehensive psychiatry 医学-精神病学
CiteScore
12.50
自引率
1.40%
发文量
64
审稿时长
29 days
期刊介绍: "Comprehensive Psychiatry" is an open access, peer-reviewed journal dedicated to the field of psychiatry and mental health. Its primary mission is to share the latest advancements in knowledge to enhance patient care and deepen the understanding of mental illnesses. The journal is supported by a diverse team of international editors and peer reviewers, ensuring the publication of high-quality research with a strong focus on clinical relevance and the implications for psychopathology. "Comprehensive Psychiatry" encourages authors to present their research in an accessible manner, facilitating engagement with clinicians, policymakers, and the broader public. By embracing an open access policy, the journal aims to maximize the global impact of its content, making it readily available to a wide audience and fostering scientific collaboration and public awareness beyond the traditional academic community. This approach is designed to promote a more inclusive and informed dialogue on mental health, contributing to the overall progress in the field.
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