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1.
Am J Med Genet B Neuropsychiatr Genet ; 180(8): 601-608, 2019 12.
Artigo em Inglês | MEDLINE | ID: mdl-30779308

RESUMO

This article provides a review of the ethical considerations that drive research policy and practice related to the genetic study of suicide. As the tenth cause of death worldwide, suicide constitutes a substantial public health concern. Biometrical studies and population-based molecular genetic studies provide compelling evidence of the utility of investigating genetic underpinnings of suicide. International, federal, and institutional policies regulating research are explored through the lenses of the ethical principles of autonomy, beneficence, non-maleficence, and justice. Trapped between the Common Rule's definition of human subjects, and the Health Insurance Portability and Accountability Act's protected information, suicide decedent data occupy an ethical gray area fraught with jurisdictional, legal, and social implications. Two avenues of research, biobanks and psychological autopsies, provide tangible application for the ethical principles examining the risks to participants and their families. Additionally, studies surveying public opinion about research methods, especially broad consent, are explored. Our approach of applying the four ethical principles to policy, sample collection, data storage, and secondary research applications can also be applied to genetic research with other populations. We conclude that broad consent for secondary research, as well as next-of-kin at the time of autopsy, serve to satisfy privacy and confidentiality under the ethical principle of autonomy. We recommend ongoing ethical evaluation of research policy and practice.


Assuntos
Bancos de Espécimes Biológicos/ética , Bases de Dados Genéticas/ética , Suicídio/ética , Confidencialidade , Pesquisa em Genética , Humanos , Autonomia Pessoal , Privacidade , Saúde Pública , Suicídio/psicologia , Estados Unidos , Prevenção do Suicídio
2.
Curr Opin Psychol ; 27: 77-81, 2019 06.
Artigo em Inglês | MEDLINE | ID: mdl-30339992

RESUMO

Psychiatric conditions are highly polygenic, meaning that genetic risk arises from many hundreds or thousands of genetic variants. Psychiatric genomics and psychological science are increasingly using polygenic risk scoring-the integration of all common genetic variant effects into a single risk metric-to model latent risk and to predict mental health outcomes. This review discusses the use of these scores in psychology and psychiatry to date, important methodological considerations, and potential of scoring methods for informing psychological science. Polygenic risk scores can easily be added to environmental and behavioral genetic models of latent risk, making them desirable metrics for use in psychological research.


Assuntos
Transtornos Mentais/genética , Biologia Molecular , Herança Multifatorial/genética , Avaliação de Resultados em Cuidados de Saúde , Humanos , Modelos Estatísticos , Psiquiatria , Fatores de Risco
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