University of California San Diego, Department of Psychiatry, La Jolla, CA, USA.
Veterans Affairs San Diego Healthcare System, Center of Excellence for Stress and Mental Health, San Diego, CA, USA.
Nat Commun. 2019 Oct 8;10(1):4558. doi: 10.1038/s41467-019-12576-w.
The risk of posttraumatic stress disorder (PTSD) following trauma is heritable, but robust common variants have yet to be identified. In a multi-ethnic cohort including over 30,000 PTSD cases and 170,000 controls we conduct a genome-wide association study of PTSD. We demonstrate SNP-based heritability estimates of 5-20%, varying by sex. Three genome-wide significant loci are identified, 2 in European and 1 in African-ancestry analyses. Analyses stratified by sex implicate 3 additional loci in men. Along with other novel genes and non-coding RNAs, a Parkinson's disease gene involved in dopamine regulation, PARK2, is associated with PTSD. Finally, we demonstrate that polygenic risk for PTSD is significantly predictive of re-experiencing symptoms in the Million Veteran Program dataset, although specific loci did not replicate. These results demonstrate the role of genetic variation in the biology of risk for PTSD and highlight the necessity of conducting sex-stratified analyses and expanding GWAS beyond European ancestry populations.
创伤后应激障碍(PTSD)的风险具有遗传性,但尚未发现强有力的常见变异。在一个包含超过 30000 例 PTSD 病例和 170000 例对照的多民族队列中,我们对 PTSD 进行了全基因组关联研究。我们证明了基于 SNP 的 PTSD 遗传率估计值为 5-20%,性别不同遗传率不同。确定了三个全基因组显著位点,其中 2 个位于欧洲人群分析中,1 个位于非洲裔人群分析中。按性别分层的分析提示男性中另外 3 个额外的位点。除了其他新的基因和非编码 RNA 外,参与多巴胺调节的帕金森病基因 PARK2 也与 PTSD 相关。最后,我们证明 PTSD 的多基因风险在百万退伍军人计划数据集的再体验症状中具有显著的预测作用,尽管特定的位点没有复制。这些结果表明遗传变异在 PTSD 风险的生物学中起作用,并强调了进行性别分层分析和扩大 GWAS 超越欧洲血统人群的必要性。