Your browser doesn't support javascript.
loading
Family secrets: Experiences and outcomes of participating in direct-to-consumer genetic relative-finder services.
Guerrini, Christi J; Robinson, Jill O; Bloss, Cinnamon C; Bash Brooks, Whitney; Fullerton, Stephanie M; Kirkpatrick, Brianne; Lee, Sandra Soo-Jin; Majumder, Mary; Pereira, Stacey; Schuman, Olivia; McGuire, Amy L.
Afiliación
  • Guerrini CJ; Center for Medical Ethics and Health Policy, Baylor College of Medicine, 1 Baylor Plaza, Houston, TX 77030, USA. Electronic address: guerrini@bcm.edu.
  • Robinson JO; Center for Medical Ethics and Health Policy, Baylor College of Medicine, 1 Baylor Plaza, Houston, TX 77030, USA.
  • Bloss CC; University of California San Diego, La Jolla, CA, 92093, USA.
  • Bash Brooks W; Center for Medical Ethics and Health Policy, Baylor College of Medicine, 1 Baylor Plaza, Houston, TX 77030, USA.
  • Fullerton SM; Department of Bioethics and Humanities, University of Washington School of Medicine, 1959 NE Pacific St, Seattle, WA 98195, USA.
  • Kirkpatrick B; Watershed DNA, PO Box 126, Crozet, VA 22932, USA.
  • Lee SS; Division of Ethics, Department of Medical Humanities and Ethics, Columbia University, 630 West 168(th) Street, PH 1525, New York, NY 10032, USA.
  • Majumder M; Center for Medical Ethics and Health Policy, Baylor College of Medicine, 1 Baylor Plaza, Houston, TX 77030, USA.
  • Pereira S; Center for Medical Ethics and Health Policy, Baylor College of Medicine, 1 Baylor Plaza, Houston, TX 77030, USA.
  • Schuman O; Center for Medical Ethics and Health Policy, Baylor College of Medicine, 1 Baylor Plaza, Houston, TX 77030, USA.
  • McGuire AL; Center for Medical Ethics and Health Policy, Baylor College of Medicine, 1 Baylor Plaza, Houston, TX 77030, USA.
Am J Hum Genet ; 109(3): 486-497, 2022 03 03.
Article en En | MEDLINE | ID: mdl-35216680
ABSTRACT
In recent decades, genetic genealogy has become popular as a result of direct-to-consumer (DTC) genetic testing. Some DTC genetic testing companies offer genetic relative-finder (GRF) services that compare the DNA of consenting participants to identify genetic relatives among them and provide each participant a list of their relative matches. We surveyed a convenience sample of GRF service participants to understand the prevalence of discoveries and associated experiences. Almost half (46%) of the 23,196 respondents had participated in GRF services only for non-specific reasons that included interest in building family trees and general curiosity. However, most (82%) also learned the identity of at least one genetic relative. Separately, most respondents (61%) reported learning something new about themselves or their relatives, including potentially disruptive information such as that a person they believed to be their biological parent is in fact not or that they have a sibling they had not known about. Respondents generally reported that discovering this new information had a neutral or positive impact on their lives, and most had low regret regarding their decision to participate in GRF services. Yet some reported making life changes as a result of their discoveries. Compared to respondents making other types of discoveries, those who learned that they were donor conceived reported the highest decisional regret and represented the largest proportion reporting net-negative consequences for themselves. Our findings indicate that discoveries from GRF services may be common and that the consequences for individuals, while generally positive, can be far-reaching and complex.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Pruebas Genéticas / Pruebas Dirigidas al Consumidor Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Am J Hum Genet Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Pruebas Genéticas / Pruebas Dirigidas al Consumidor Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Am J Hum Genet Año: 2022 Tipo del documento: Article