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GWAS Study

Genome-wide association study identifies four pan-ancestry loci for suicidal ideation in the Million Veterans Program.

Ashley-Koch AE, Kimbrel NA, Qin XJ et al.

36940203 PubMed ID
GWAS Study Type
612381 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

AA
Ashley-Koch AE
KN
Kimbrel NA
QX
Qin XJ
LJ
Lindquist JH
GM
Garrett ME
DM
Dennis MF
HL
Hair LP
HJ
Huffman JE
JD
Jacobson DA
MR
Madduri RK
CH
Coon H
DA
Docherty AR
KJ
Kang J
MN
Mullins N
RD
Ruderfer DM
HP
Harvey PD
MB
McMahon BH
OD
Oslin DW
HE
Hauser ER
HM
Hauser MA
BJ
Beckham JC
Chapter II

Abstract

Summary of the research findings

Suicidal ideation (SI) often precedes and predicts suicide attempt and death, is the most common suicidal phenotype and is over-represented in veterans. The genetic architecture of SI in the absence of suicide attempt (SA) is unknown, yet believed to have distinct and overlapping risk with other suicidal behaviors. We performed the first GWAS of SI without SA in the Million Veteran Program (MVP), identifying 99,814 SI cases from electronic health records without a history of SA or suicide death (SD) and 512,567 controls without SI, SA or SD. GWAS was performed separately in the four largest ancestry groups, controlling for sex, age and genetic substructure. Ancestry-specific results were combined via meta-analysis to identify pan-ancestry loci. Four genome-wide significant (GWS) loci were identified in the pan-ancestry meta-analysis with loci on chromosomes 6 and 9 associated with suicide attempt in an independent sample. Pan-ancestry gene-based analysis identified GWS associations with DRD2, DCC, FBXL19, BCL7C, CTF1, ANNK1, and EXD3. Gene-set analysis implicated synaptic and startle response pathways (q's<0.05). European ancestry (EA) analysis identified GWS loci on chromosomes 6 and 9, as well as GWS gene associations in EXD3, DRD2, and DCC. No other ancestry-specific GWS results were identified, underscoring the need to increase representation of diverse individuals. The genetic correlation of SI and SA within MVP was high (rG = 0.87; p = 1.09e-50), as well as with post-traumatic stress disorder (PTSD; rG = 0.78; p = 1.98e-95) and major depressive disorder (MDD; rG = 0.78; p = 8.33e-83). Conditional analysis on PTSD and MDD attenuated most pan-ancestry and EA GWS signals for SI without SA to nominal significance, with the exception of EXD3 which remained GWS. Our novel findings support a polygenic and complex architecture for SI without SA which is largely shared with SA and overlaps with psychiatric conditions frequently comorbid with suicidal behaviors.

62,023 European ancestry cases, 376,826 European ancestry controls, 25,097 African American cases, 90,835 African American controls, 1,529 Asian ancestry cases, 6,528 Asian ancestry controls, 11,165 Hispanic or Latin American cases, 38,378 Hispanic or Latin American controls

Chapter III

Study Statistics

Key metrics and study information

612381
Total Participants
GWAS
Study Type
No
Replicated
European, African American or Afro-Caribbean, Asian unspecified, Hispanic or Latin American
Ancestry
U.S.
Recruitment Country
Chapter IV

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