Menu
GWAS Study

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

Stein MB, Levey DF, Cheng Z et al.

33510476 PubMed ID
GWAS Study Type
389067 Participants
Scroll to explore
Chapter I

Publication Details

Comprehensive information about this research publication

Authors

SM
Stein MB
LD
Levey DF
CZ
Cheng Z
WF
Wendt FR
HK
Harrington K
PG
Pathak GA
CK
Cho K
QR
Quaden R
RK
Radhakrishnan K
GM
Girgenti MJ
HY
Ho YA
PD
Posner D
AM
Aslan M
DR
Duman RS
ZH
Zhao H
PR
Polimanti R
CJ
Concato J
GJ
Gelernter J
Chapter II

Abstract

Summary of the research findings

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.

36,301 European ancestry cases, 178,107 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

389067
Total Participants
GWAS
Study Type
Yes
Replicated
23,212 European ancestry cases, 151,447 European ancestry controls
Replication Participants
European, African unspecified
Ancestry
U.S.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

Important Disclaimer: This review has been performed semi-automatically and is provided for informational purposes only. While we strive for accuracy, this analysis may contain errors, omissions, or misinterpretations of the original research. DNA Genics disclaims all liability for any inaccuracies, errors, or consequences arising from the use of this information. Users should independently verify all information and consult original research publications before making any decisions based on this content. This analysis is not intended as a substitute for professional scientific review or medical advice.

Analysis In Progress

Our analysis of this publication is currently being prepared. Please check back soon for comprehensive insights into the health and genetic findings discussed in this research.