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dc.contributor.authorDocherty, Anna R.
dc.contributor.authorMullins, Niamh
dc.contributor.authorAshley-Koch, Allison E.
dc.contributor.authorQin, Xuejun
dc.contributor.authorColeman, Jonathan R.I.
dc.contributor.authorShabalin, Andrey
dc.contributor.authorKang, JooEun
dc.contributor.authorMurnyak, Balasz
dc.contributor.authorWendt, Frank
dc.contributor.authorAdams, Mark
dc.contributor.authorCampos, Adrian I.
dc.contributor.authorDiBlasi, Emily
dc.contributor.authorFullerton, Janice M.
dc.contributor.authorKranzler, Henry R.
dc.contributor.authorBakian, Amanda V.
dc.contributor.authorMonson, Eric T.
dc.contributor.authorRentería, Miguel E.
dc.contributor.authorWalss-Bass, Consuelo
dc.contributor.authorAndreassen, Ole
dc.contributor.authorBehera, Chittaranjan
dc.contributor.authorBulik, Cynthia M.
dc.contributor.authorEdenberg, Howard J.
dc.contributor.authorAdolfsson, Rolf
dc.contributor.authorAgartz, Ingrid
dc.contributor.authorAlda, Martin
dc.contributor.authorAlfredsson, Lars
dc.contributor.authorAppadurai, Vivek
dc.contributor.authorArtigas, María Soler
dc.contributor.authorDjurovic, Srdjan
dc.contributor.authorFoo, Jerome C.
dc.contributor.authorForstner, Andreas J.
dc.contributor.authorFrye, Mark
dc.contributor.authorGatt, Justine
dc.contributor.authorMelle, Ingrid
dc.contributor.authorMitchell, Philip B.
dc.contributor.authorMolina, Esther
dc.contributor.authorMorken, Gunnar
dc.contributor.authorSmeland, Olav Bjerkehagen
dc.contributor.authorSmoller, Jordan W.
dc.contributor.authorSonuga-Barke, Edmund J.S.
dc.contributor.authorTrzaskowski, Maciej
dc.contributor.authorTsuang, Ming T.
dc.contributor.authorTurecki, Gustavo
dc.contributor.authorVilar-Ribó, Laura
dc.contributor.authorVincent, John B.
dc.contributor.authorVölzke, Henry
dc.contributor.authorWalters, James T.R.
dc.contributor.authorWeickert, Cynthia Shannon
dc.contributor.authorWeickert, Thomas W.
dc.contributor.authorWeissman, Myrna M.
dc.date.accessioned2024-02-22T10:21:47Z
dc.date.available2024-02-22T10:21:47Z
dc.date.created2024-02-20T14:18:15Z
dc.date.issued2023
dc.identifier.citationAmerican Journal of Psychiatry. 2023, 180 (10), 723-738.en_US
dc.identifier.issn0002-953X
dc.identifier.urihttps://hdl.handle.net/11250/3119266
dc.description.abstractObjective: Suicidal behavior is heritable and is a major cause of death worldwide. Two large-scale genome-wide association studies (GWASs) recently discovered and cross-validated genome-wide significant (GWS) loci for suicide attempt (SA). The present study leveraged the genetic cohorts from both studies to conduct the largest GWAS meta-analysis 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.en_US
dc.language.isoengen_US
dc.publisherAmerican Psychiatric Associationen_US
dc.titleGWAS Meta-Analysis of Suicide Attempt: Identification of 12 Genome-Wide Significant Loci and Implication of Genetic Risks for Specific Health Factorsen_US
dc.title.alternativeGWAS Meta-Analysis of Suicide Attempt: Identification of 12 Genome-Wide Significant Loci and Implication of Genetic Risks for Specific Health Factorsen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.rights.holder© 2024 American Psychiatric Associationen_US
dc.source.pagenumber723-738en_US
dc.source.volume180en_US
dc.source.journalAmerican Journal of Psychiatryen_US
dc.source.issue10en_US
dc.identifier.doi10.1176/appi.ajp.21121266
dc.identifier.cristin2248124
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2


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