VA San Diego Healthcare System, Psychiatry Service, San Diego, CA, USA.
Department of Psychiatry, University of California San Diego, La Jolla, CA, USA.
Nat Genet. 2021 Feb;53(2):174-184. doi: 10.1038/s41588-020-00767-x. Epub 2021 Jan 28.
We conducted genome-wide association analyses of over 250,000 participants of European (EUR) and African (AFR) ancestry from the Million Veteran Program using electronic health record-validated post-traumatic stress disorder (PTSD) diagnosis and quantitative symptom phenotypes. Applying genome-wide multiple testing correction, we identified three significant loci in European case-control analyses and 15 loci in quantitative symptom analyses. Genomic structural equation modeling indicated tight coherence of a PTSD symptom factor that shares genetic variance with a distinct internalizing (mood-anxiety-neuroticism) factor. Partitioned heritability indicated enrichment in several cortical and subcortical regions, and imputed genetically regulated gene expression in these regions was used to identify potential drug repositioning candidates. These results validate the biological coherence of the PTSD syndrome, inform its relationship to comorbid anxiety and depressive disorders and provide new considerations for treatment.
我们利用百万退伍军人计划中 25 万多名具有欧洲(EUR)和非洲(AFR)血统的参与者的全基因组关联分析,使用电子健康记录验证的创伤后应激障碍(PTSD)诊断和定量症状表型。通过全基因组多重测试校正,我们在欧洲病例对照分析中确定了三个显著位点,在定量症状分析中确定了 15 个位点。基因组结构方程模型表明,PTSD 症状因子与一个独特的内化(情绪-焦虑-神经质)因子具有紧密的遗传相关性。分割遗传率表明,在几个皮质和皮质下区域富集,并且在这些区域中推断出遗传调控的基因表达,以识别潜在的药物重新定位候选物。这些结果验证了 PTSD 综合征的生物学一致性,告知其与共病焦虑和抑郁障碍的关系,并为治疗提供了新的考虑因素。