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Bi-ancestral depression GWAS in the Million Veteran Program and meta-analysis in >1.2 million individuals highlight new therapeutic directions.

Levey DF, Stein MB, Wendt FR et al.

34045744 PubMed ID
GWAS Study Type
250215 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

LD
Levey DF
SM
Stein MB
WF
Wendt FR
PG
Pathak GA
ZH
Zhou H
AM
Aslan M
QR
Quaden R
HK
Harrington KM
NY
Nuñez YZ
OC
Overstreet C
RK
Radhakrishnan K
SG
Sanacora G
MA
McIntosh AM
SJ
Shi J
SS
Shringarpure SS
CJ
Concato J
PR
Polimanti R
GJ
Gelernter J
Chapter II

Abstract

Summary of the research findings

Major depressive disorder is the most common neuropsychiatric disorder, affecting 11% of veterans. Here we report results of a large meta-analysis of depression using data from the Million Veteran Program, 23andMe, UK Biobank and FinnGen, including individuals of European ancestry (n = 1,154,267; 340,591 cases) and African ancestry (n = 59,600; 25,843 cases). Transcriptome-wide association study analyses revealed significant associations with expression of NEGR1 in the hypothalamus and DRD2 in the nucleus accumbens, among others. We fine-mapped 178 genomic risk loci, and we identified likely pathogenicity in these variants and overlapping gene expression for 17 genes from our transcriptome-wide association study, including TRAF3. Finally, we were able to show substantial replications of our findings in a large independent cohort (n = 1,342,778) provided by 23andMe. This study sheds light on the genetic architecture of depression and provides new insight into the interrelatedness of complex psychiatric traits.

83,810 European ancestry cases, 166,405 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

250215
Total Participants
GWAS
Study Type
Yes
Replicated
455,350 cases, 887,428 controls
Replication Participants
European, African American or Afro-Caribbean
Ancestry
U.S., U.K.
Recruitment Country
Chapter IV

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