TY - JOUR
T1 - GWAS Meta-Analysis of Suicide Attempt
T2 - Identification of 12 Genome-Wide Significant Loci and Implication of Genetic Risks for Specific Health Factors
AU - Docherty, Anna R
AU - Mullins, Niamh
AU - Ashley-Koch, Allison E
AU - Qin, Xuejun
AU - Coleman, Jonathan R I
AU - Shabalin, Andrey
AU - Kang, JooEun
AU - Murnyak, Balasz
AU - Wendt, Frank
AU - Adams, Mark
AU - Campos, Adrian I
AU - DiBlasi, Emily
AU - Fullerton, Janice M
AU - Kranzler, Henry R
AU - Bakian, Amanda V
AU - Monson, Eric T
AU - Rentería, Miguel E
AU - Walss-Bass, Consuelo
AU - Andreassen, Ole A
AU - Behera, Chittaranjan
AU - Bulik, Cynthia M
AU - Edenberg, Howard J
AU - Kessler, Ronald C
AU - Mann, J John
AU - Nurnberger, John I
AU - Pistis, Giorgio
AU - Streit, Fabian
AU - Ursano, Robert J
AU - Polimanti, Renato
AU - Dennis, Michelle
AU - Garrett, Melanie
AU - Hair, Lauren
AU - Harvey, Philip
AU - Hauser, Elizabeth R
AU - Hauser, Michael A
AU - Huffman, Jennifer
AU - Jacobson, Daniel
AU - Madduri, Ravi
AU - McMahon, Benjamin
AU - Oslin, David W
AU - Trafton, Jodie
AU - Awasthi, Swapnil
AU - Berrettini, Wade H
AU - Bohus, Martin
AU - Chang, Xiao
AU - Chen, Hsi-Chung
AU - Boks, Marco P
AU - Cahn, Wiepke
AU - Kahn, René S
AU - Ophoff, Roel A
N1 - Publisher Copyright:
© 2023 American Psychiatric Association. All rights reserved.
PY - 2023/10/1
Y1 - 2023/10/1
N2 - Objective: Suicidal behavior is heritable and is a major cause of death worldwide. Two large-scale genome-wide association studies (GWASs) recently discovered and crossvalidated genome-wide significant (GWS) loci for suicide attempt (SA). The present study leveraged the genetic cohorts from both studies to conduct the largest GWAS metaanalysis of SA to date. Multi-ancestry and admixture-specific meta-analyses were conducted within groups of significant African, East Asian, and European ancestry admixtures. Methods: This study comprised 22 cohorts, including 43,871 SA cases and 915,025 ancestry-matched controls. Analytical methods across multi-ancestry and individual ancestry admixtures included inverse variance-weighted fixed-effects meta-analyses, followed by gene, gene-set, tissue-set, and drug-target enrichment, as well as summary-data-based Mendelian randomization with brain expression quantitative trait loci data, phenome-wide genetic correlation, and genetic causal proportion analyses. Results: Multi-ancestry and European ancestry admixture GWAS meta-analyses identified 12 risk loci at p values <5×10-8. These loci were mostly intergenic and implicated DRD2, SLC6A9, FURIN, NLGN1, SOX5, PDE4B, and CACNG2. The multi-ancestry SNP-based heritability estimate of SA was 5.7% on the liability scale (SE=0.003, p=5.7×10-80). Significant brain tissue gene expression and drug set enrichment were observed. There was shared genetic variation of SA with attention deficit hyperactivity disorder, smoking, and risk tolerance after conditioning SA on both major depressive disorder and posttraumatic stress disorder. Genetic causal proportion analyses implicated shared genetic risk for specific health factors. Conclusions: This multi-ancestry analysis of suicide attempt identified several loci contributing to risk and establishes significant shared genetic covariation with clinical phenotypes. These findings provide insight into genetic factors associated with suicide attempt across ancestry admixture populations, in veteran and civilian populations, and in attempt versus death.
AB - Objective: Suicidal behavior is heritable and is a major cause of death worldwide. Two large-scale genome-wide association studies (GWASs) recently discovered and crossvalidated genome-wide significant (GWS) loci for suicide attempt (SA). The present study leveraged the genetic cohorts from both studies to conduct the largest GWAS metaanalysis of SA to date. Multi-ancestry and admixture-specific meta-analyses were conducted within groups of significant African, East Asian, and European ancestry admixtures. Methods: This study comprised 22 cohorts, including 43,871 SA cases and 915,025 ancestry-matched controls. Analytical methods across multi-ancestry and individual ancestry admixtures included inverse variance-weighted fixed-effects meta-analyses, followed by gene, gene-set, tissue-set, and drug-target enrichment, as well as summary-data-based Mendelian randomization with brain expression quantitative trait loci data, phenome-wide genetic correlation, and genetic causal proportion analyses. Results: Multi-ancestry and European ancestry admixture GWAS meta-analyses identified 12 risk loci at p values <5×10-8. These loci were mostly intergenic and implicated DRD2, SLC6A9, FURIN, NLGN1, SOX5, PDE4B, and CACNG2. The multi-ancestry SNP-based heritability estimate of SA was 5.7% on the liability scale (SE=0.003, p=5.7×10-80). Significant brain tissue gene expression and drug set enrichment were observed. There was shared genetic variation of SA with attention deficit hyperactivity disorder, smoking, and risk tolerance after conditioning SA on both major depressive disorder and posttraumatic stress disorder. Genetic causal proportion analyses implicated shared genetic risk for specific health factors. Conclusions: This multi-ancestry analysis of suicide attempt identified several loci contributing to risk and establishes significant shared genetic covariation with clinical phenotypes. These findings provide insight into genetic factors associated with suicide attempt across ancestry admixture populations, in veteran and civilian populations, and in attempt versus death.
UR - http://www.scopus.com/inward/record.url?scp=85176353814&partnerID=8YFLogxK
U2 - 10.1176/appi.ajp.21121266
DO - 10.1176/appi.ajp.21121266
M3 - Article
C2 - 37777856
SN - 0002-953X
VL - 180
SP - 723
EP - 738
JO - American Journal of Psychiatry
JF - American Journal of Psychiatry
IS - 10
ER -