Katalog Plus
Bibliothek der Frankfurt UAS
Bald neuer Katalog: sichern Sie sich schon vorab Ihre persönlichen Merklisten im Nutzerkonto: Anleitung.
Dieses Ergebnis aus BASE kann Gästen nicht angezeigt werden.  Login für vollen Zugriff.

Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors

Title: Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors
Authors: Mullins, N; Kang, JE; Campos, AI; Coleman, JRI; Edwards, AC; Galfalvy, H; Levey, DF; Lori, A; Shabalin, A; Starnawska, A; Su, MH; Watson, HJ; Adams, M; Awasthi, S; Gandal, M; Hafferty, JD; Hishimoto, A; Kim, M; Okazaki, S; Otsuka, I; Ripke, S; Ware, EB; Bergen, AW; Berrettini, WH; Bohus, M; Brandt, H; Chang, X; Chen, WJ; Chen, HC; Crawford, S; Crow, S; DiBlasi, E; Duriez, P; Fernández-Aranda, F; Fichter, MM; Gallinger, S; Glatt, SJ; Gorwood, P; Guo, Y; Hakonarson, H; Halmi, KA; Hwu, HG; Jain, S; Jamain, S; Jiménez-Murcia, S; Johnson, C; Kaplan, AS; Kaye, WH; Keel, PK; Kennedy, JL; Klump, KL; Li, D; Liao, SC; Lieb, K; Lilenfeld, L; Liu, CM; Magistretti, PJ; Marshall, CR; Mitchell, JE; Monson, ET; Myers, RM; Pinto, D; Powers, A; Ramoz, N; Roepke, S; Rozanov, V; Scherer, SW; Schmahl, C; Sokolowski, M; Strober, M; Thornton, LM; Treasure, J; Tsuang, MT; Witt, SH; Woodside, DB; Yilmaz, Z; Zillich, L; Adolfsson, R; Agartz, I; Air, TM; Alda, M; Alfredsson, L; Andreassen, OA; Anjorin, A; Appadurai, V; Soler Artigas, M; Van der Auwera, S; Azevedo, MH; Bass, N; Bau, CHD; Baune, BT; Bellivier, F; Berger, K; Biernacka, JM; Bigdeli, TB; Binder, EB; Boehnke, M; Boks, MP; Bosch, R; Braff, DL; Fullerton, Janice; Shannon Weickert, Cynthia; Gatt, Justine; Schofield, Peter; Mitchell, Philip; Green, Melissa; Roberts, Gloria; Carr, Vaughan; Smith, Daniel; Toma, Claudio
Source: urn:ISSN:0006-3223 ; urn:ISSN:1873-2402 ; Biological Psychiatry, 91, 3, 313-327
Publisher Information: Elsevier
Publication Year: 2022
Collection: UNSW Sydney (The University of New South Wales): UNSWorks
Subject Terms: 5202 Biological Psychology; 31 Biological Sciences; 3105 Genetics; 52 Psychology; Brain Disorders; Genetics; Human Genome; Mental Illness; Depression; Basic Behavioral and Social Science; Serious Mental Illness; Sleep Research; Behavioral and Social Science; Suicide; Mental Health; Prevention; 2.3 Psychological; social and economic factors; 3 Good Health and Well Being; Major Depressive Disorder; Genome-Wide Association Study; Humans; Mental Disorders; Polymorphism; Single Nucleotide; Risk Factors; Attempted; Genetic correlation; Pleiotropy; Polygenicity
Description: Background: Suicide is a leading cause of death worldwide, and nonfatal suicide attempts, which occur far more frequently, are a major source of disability and social and economic burden. Both have substantial genetic etiology, which is partially shared and partially distinct from that of related psychiatric disorders. Methods: We conducted a genome-wide association study (GWAS) of 29,782 suicide attempt (SA) cases and 519,961 controls in the International Suicide Genetics Consortium (ISGC). The GWAS of SA was conditioned on psychiatric disorders using GWAS summary statistics via multitrait-based conditional and joint analysis, to remove genetic effects on SA mediated by psychiatric disorders. We investigated the shared and divergent genetic architectures of SA, psychiatric disorders, and other known risk factors. Results: Two loci reached genome-wide significance for SA: the major histocompatibility complex and an intergenic locus on chromosome 7, the latter of which remained associated with SA after conditioning on psychiatric disorders and replicated in an independent cohort from the Million Veteran Program. This locus has been implicated in risk-taking behavior, smoking, and insomnia. SA showed strong genetic correlation with psychiatric disorders, particularly major depression, and also with smoking, pain, risk-taking behavior, sleep disturbances, lower educational attainment, reproductive traits, lower socioeconomic status, and poorer general health. After conditioning on psychiatric disorders, the genetic correlations between SA and psychiatric disorders decreased, whereas those with nonpsychiatric traits remained largely unchanged. Conclusions: Our results identify a risk locus that contributes more strongly to SA than other phenotypes and suggest a shared underlying biology between SA and known risk factors that is not mediated by psychiatric disorders.
Document Type: article in journal/newspaper
File Description: application/pdf
Language: unknown
Relation: https://hdl.handle.net/1959.4/unsworks_83420; https://doi.org/10.1016/j.biopsych.2021.05.029
DOI: 10.1016/j.biopsych.2021.05.029
Availability: https://hdl.handle.net/1959.4/unsworks_83420; https://unsworks.unsw.edu.au/bitstreams/306a4f2b-9ecb-4474-9791-84f8344241aa/download; https://doi.org/10.1016/j.biopsych.2021.05.029
Rights: open access ; https://purl.org/coar/access_right/c_abf2 ; CC BY-NC-ND ; https://creativecommons.org/licenses/by-nc-nd/4.0/ ; free_to_read ; This article is available under the Creative Commons CC-BY-NC-ND license and permits non-commercial use of the work as published, without adaptation or alteration provided the work is fully attributed.
Accession Number: edsbas.D172416D
Database: BASE