Genome-wide association analyses of post-traumatic stress disorder and its symptom subdomains in the Million Veteran Program

被引:0
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作者
Murray B. Stein
Daniel F. Levey
Zhongshan Cheng
Frank R. Wendt
Kelly Harrington
Gita A. Pathak
Kelly Cho
Rachel Quaden
Krishnan Radhakrishnan
Matthew J. Girgenti
Yuk-Lam Anne Ho
Daniel Posner
Mihaela Aslan
Ronald S. Duman
Hongyu Zhao
Renato Polimanti
John Concato
Joel Gelernter
机构
[1] VA San Diego Healthcare System,Department of Psychiatry
[2] Psychiatry Service,Department of Psychiatry
[3] University of California San Diego,Department of Psychiatry
[4] Herbert Wertheim School of Public Health and Human Longevity Science,Department of Medicine
[5] University of California San Diego,Department of Medicine
[6] VA Connecticut Healthcare System,Department of Biostatistics
[7] Psychiatry Service,undefined
[8] Yale University School of Medicine,undefined
[9] VA Boston Healthcare System,undefined
[10] Massachusetts Veterans Epidemiology Research and Information Center,undefined
[11] Boston University School of Medicine,undefined
[12] Brigham and Women’s Hospital,undefined
[13] Clinical Epidemiology Research Center,undefined
[14] VA Connecticut Healthcare System,undefined
[15] College of Medicine,undefined
[16] University of Kentucky,undefined
[17] Office of the Director,undefined
[18] Center for Behavioral Health Statistics and Quality,undefined
[19] Substance Abuse and Mental Health Services Administration,undefined
[20] Yale University School of Medicine,undefined
[21] Yale University School of Public Health,undefined
[22] Food and Drug Administration,undefined
[23] Center for Drug Evaluation and Research,undefined
来源
Nature Genetics | 2021年 / 53卷
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摘要
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.
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页码:174 / 184
页数:10
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