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Choices, attitudes, and experiences of genetic screening in Latino/a and Ashkenazi Jewish individuals.
Reed-Weston, Anne E; Espinal, Aileen; Hasar, Bianca; Chiuzan, Codruta; Lazarin, Gabriel; Weng, Chunhua; Appelbaum, Paul S; Chung, Wendy K; Wynn, Julia.
Afiliação
  • Reed-Weston AE; Vagelos College of Physician & Surgeons, Columbia Irving University, New York, NY, USA.
  • Espinal A; Department of Pediatrics, Columbia University Irving Medical Center, New York, NY, USA.
  • Hasar B; Department of Pediatrics, Columbia University Irving Medical Center, New York, NY, USA.
  • Chiuzan C; Department of Biostatistics, Columbia University Irving Medical Center, New York, NY, USA.
  • Lazarin G; Department of Biomedical Informatics, Columbia University Irving Medical Center, New York, NY, USA.
  • Weng C; Myriad Women's Health (Formerly Counsyl), South San Francisco, CA, USA.
  • Appelbaum PS; Department of Psychiatry, Columbia University Irving Medical Center, New York, NY, USA.
  • Chung WK; Department of Pediatrics, Columbia University Irving Medical Center, New York, NY, USA.
  • Wynn J; Department of Medicine, Columbia University Medical Irving Center, New York, NY, USA.
J Community Genet ; 11(4): 391-403, 2020 Oct.
Article em En | MEDLINE | ID: mdl-32382939
Genetic screening to inform personal risk has only recently become an option as the cost of sequencing decreases, and our ability to interpret sequence variants improves. Studies have demonstrated that people want to learn about their genetic information and do well after learning it, but minorities are underrepresented in these studies. We surveyed Ashkenazi Jewish (AJ) and Latino/a participants in a genetic screening study to solicit choices about genetic results to return, as well as their experience with learning these results and attitudes about genetic information secrecy and security. Participants had the option to proceed through the study self-guided, and few elected to have traditional pre-test genetic education and counseling. Despite this, the majority were satisfied with the process of selecting and receiving genetic results and felt that they understood their results. Concerns about privacy and confidentiality of genetic data were minimal, though some participants expressed modest concerns about keeping any potential results secret or the confidentiality of their genetic information. Our results support the feasibility of the option of self-guided genetic screening. Additional care will need to be taken when designing population-based screening studies to meet the needs of participants who come from communities with different experiences with genetics.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Qualitative_research / Screening_studies Idioma: En Revista: J Community Genet Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Qualitative_research / Screening_studies Idioma: En Revista: J Community Genet Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos