Moo-Choy Ashley, Stein Murray B, Gelernter Joel, Wendt Frank R
Department of Anthropology, University of Toronto, Toronto, ON, Canada.
Forensic Science Program, University of Toronto, Mississauga, ON, Canada.
Can J Psychiatry. 2025 Feb;70(2):117-126. doi: 10.1177/07067437241301016. Epub 2024 Dec 9.
Posttraumatic stress disorder (PTSD) affects 3.9%-5.6% of the worldwide population, with well-documented sex-related differences. While psychosocial and hormonal factors affecting sex differences in PTSD and posttraumatic stress (PTS) symptom etiology have been explored, there has been limited focus on the genetic bases of these differences. Many symptom combinations may confer a PTSD diagnosis. We hypothesized that these symptom combinations have sex-specific patterns, the examination of which could inform etiological differences in PTSD genetics between males and females.
To investigate this, we performed a sex-stratified multivariate genome-wide association study (GWAS) in unrelated UK Biobank (UKB) individuals of European ancestry. Using GWAS summary association data, genomic structural equation modelling was performed to generate sex-specific factor models using 6 indicator variables: trouble concentrating, feeling distant from others, irritability, disturbing thoughts, upset feelings, and avoidance of places/activities which remind the individual of a traumatic event.
Models of male and female PTSD symptoms differed substantially (local standardized root mean square difference = 3.12) and significantly (χ(5) = 28.03, = 3.6 × 10). Independent 2-factor models best fit the data in both males and females; these factors were subjected to GWAS in each sex, revealing 3 genome-wide significant loci in females, mapping to , , and . No genome-wide significant loci were identified in males. All 4 PTS factors (2 in males and 2 in females) were heritable.
By assessing the relationship between sex and PTSD symptoms, this study informs correlative and putatively causal etiological differences between males and females which support further investigation of sex differences in PTSD genetics.
创伤后应激障碍(PTSD)影响着全球3.9%-5.6%的人口,其与性别相关的差异有充分记录。虽然影响PTSD性别差异以及创伤后应激(PTS)症状病因的心理社会和激素因素已得到探索,但对这些差异的遗传基础关注有限。许多症状组合可能导致PTSD诊断。我们假设这些症状组合具有性别特异性模式,对其进行研究可以揭示男性和女性PTSD遗传学的病因差异。
为了对此进行研究,我们在欧洲血统的非亲属英国生物银行(UKB)个体中进行了性别分层的多变量全基因组关联研究(GWAS)。利用GWAS汇总关联数据,进行基因组结构方程建模,使用6个指标变量生成性别特异性因子模型:注意力不集中、感觉与他人疏远、易怒、困扰性想法、心烦意乱的情绪以及避免前往/参与会让个体想起创伤事件的场所/活动。
男性和女性PTSD症状模型存在显著差异(局部标准化均方根差异 = 3.12)且具有统计学意义(χ(5) = 28.03,P = 3.6×10)。独立的双因子模型最适合男性和女性的数据;对这些因子在每种性别中进行GWAS分析,在女性中发现了3个全基因组显著位点,分别映射到……。在男性中未发现全基因组显著位点。所有4个PTS因子(男性2个,女性2个)都是可遗传的。
通过评估性别与PTSD症状之间的关系,本研究揭示了男性和女性之间的相关及可能的因果病因差异,支持进一步研究PTSD遗传学中的性别差异。