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GWAS Study

Genomewide association studies of suicide attempts in US soldiers.

Stein MB, Ware EB, Mitchell C et al.

28902444 PubMed ID
GWAS Study Type
15923 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

SM
Stein MB
WE
Ware EB
MC
Mitchell C
CC
Chen CY
BS
Borja S
CT
Cai T
DC
Dempsey CL
FC
Fullerton CS
GJ
Gelernter J
HS
Heeringa SG
JS
Jain S
KR
Kessler RC
NJ
Naifeh JA
NM
Nock MK
RS
Ripke S
SX
Sun X
BJ
Beckham JC
KN
Kimbrel NA
UR
Ursano RJ
SJ
Smoller JW
Chapter II

Abstract

Summary of the research findings

Suicide is a global public health problem with particular resonance for the US military. Genetic risk factors for suicidality are of interest as indicators of susceptibility and potential targets for intervention. We utilized population-based nonclinical cohorts of US military personnel (discovery: N = 473 cases and N = 9778 control subjects; replication: N = 135 cases and N = 6879 control subjects) and a clinical case-control sample of recent suicide attempters (N = 51 cases and N = 112 control subjects) to conduct GWAS of suicide attempts (SA). Genomewide association was evaluated within each ancestral group (European-, African-, Latino-American) and study using logistic regression models. Meta-analysis of the European ancestry discovery samples revealed a genomewide significant locus in association with SA near MRAP2 (melanocortin 2 receptor accessory protein 2) and CEP162 (centrosomal protein 162); 12 genomewide significant SNPs in the region; peak SNP rs12524136-T, OR = 2.88, p = 5.24E-10. These findings were not replicated in the European ancestry subsamples of the replication or suicide attempters samples. However, the association of the peak SNP remained significant in a meta-analysis of all studies and ancestral subgroups (OR = 2.18, 95%CI 1.70, 2.80). Polygenic risk score (PRS) analyses showed some association of SA with bipolar disorder. The association with SNPs encompassing MRAP2, a gene expressed in brain and adrenal cortex and involved in neural control of energy homeostasis, points to this locus as a plausible susceptibility gene for suicidality that should be further studied. Larger sample sizes will be needed to confirm and extend these findings.

311 European ancestry cases, 83 African cases, 79 Hispanic/Latino cases, 6,228 European ancestry controls, 1,689 African controls, 1,861 Hispanic/Latino controls

Chapter III

Study Statistics

Key metrics and study information

15923
Total Participants
GWAS
Study Type
Yes
Replicated
89 European ancestry cases, 17 African cases, 29 Hispanic/Latino cases, 4,594 European ancestry controls, 823 African controls, 1,462 Hispanic/Latino controls
Replication Participants
Hispanic or Latin American, European, African unspecified
Ancestry
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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Analysis In Progress

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