GWAS Meta-Analysis of Suicide Attempt: Identification of 12 Genome-Wide Significant Loci and Implication of Genetic Risks for Specific Health Factors

被引:42
作者
Docherty, Anna R.
Mullins, Niamh
Ashley-Koch, Allison E.
Qin, Xuejun
Coleman, Jonathan R. I.
Shabalin, Andrey
Kang, JooEun
Murnyak, Balasz
Wendt, Frank
Adams, Mark
Campos, Adrian I.
DiBlasi, Emily
Fullerton, Janice M.
Kranzler, Henry R.
Bakian, Amanda V.
Monson, Eric T.
Renteria, Miguel E.
Walss-Bass, Consuelo
Andreassen, Ole A.
Behera, Chittaranjan
Bulik, Cynthia M.
Edenberg, Howard J.
Kessler, Ronald C.
Mann, J. John
Nurnberger, John I., Jr.
Pistis, Giorgio
Streit, Fabian
Ursano, Robert J.
Polimanti, Renato
Dennis, Michelle
Garrett, Melanie
Hair, Lauren
Harvey, Philip
Hauser, Elizabeth R.
Hauser, Michael A.
Huffman, Jennifer
Jacobson, Daniel
Madduri, Ravi
McMahon, Benjamin
Oslin, David W.
Trafton, Jodie
Awasthi, Swapnil
Berrettini, Wade H.
Bohus, Martin
Chang, Xiao
Chen, Hsi-Chung
Chen, Wei J.
Christensen, Erik D.
Crow, Scott
Duriez, Philibert
机构
关键词
LD SCORE REGRESSION; ASSOCIATION; HERITABILITY; NETWORK; SEX;
D O I
10.1176/appi.ajp.21121266
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Objective: Suicidal behavior is heritable and is a major causeof 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 < 5x10(-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=5.7x10(-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.
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收藏
页码:723 / 738
页数:16
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