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Genetic contributions to suicidal thoughts and behaviors

期刊

PSYCHOLOGICAL MEDICINE
卷 51, 期 13, 页码 2148-2155

出版社

CAMBRIDGE UNIV PRESS
DOI: 10.1017/S0033291721001720

关键词

Suicide; suicide attempt; suicidal ideation; suicidal thoughts and behaviors; genetics; genetic epidemiology

资金

  1. American Foundation for Suicide Prevention [PDF-0-038-18]
  2. National Institute of Mental Health [R01 MH123619, R01 MH123498]

向作者/读者索取更多资源

Suicidal ideation, suicide attempt, and suicide are significantly heritable phenotypes, but the extent to which they share genetic architecture is unclear. Recent studies have shifted focus from suicide within the context of major psychopathology to suicide as an independent entity, identifying significant loci associated with suicide and examining them within and outside of major psychopathology. Additionally, polygenic risk scores have shown associations with case-control status and other risk phenotypes.
Suicidal ideation, suicide attempt (SA) and suicide are significantly heritable phenotypes. However, the extent to which these phenotypes share genetic architecture is unclear. This question is of great relevance to determining key risk factors for suicide, and to alleviate the societal burden of suicidal thoughts and behaviors (STBs). To help address the question of heterogeneity, consortia efforts have recently shifted from a focus on suicide within the context of major psychopathology (e.g. major depressive disorder, schizophrenia) to suicide as an independent entity. Recent molecular studies of suicide risk by members of the Psychiatric Genomics Consortium and the International Suicide Genetics Consortium have identified genome-wide significant loci associated with SA and with suicide death, and have examined these phenotypes within and outside of the context of major psychopathology. This review summarizes important insights from epidemiological and biometrical research on suicide, and discusses key empirical findings from molecular genetic examinations of STBs. Polygenic risk scores for these phenotypes have been observed to be associated with case-control status and other risk phenotypes. In addition, estimated shared genetic covariance with other phenotypes suggests specific medical and psychiatric risks beyond major depressive disorder. Broadly, molecular studies suggest a complexity of suicide etiology that cannot simply be accounted for by depression. Discussion of the state of suicide genetics, a growing field, also includes important ethical and clinical implications of studying the genetic risk of suicide.

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