Returning genetic research results: study type matters

Author:

McGuire Amy L1,Robinson Jill Oliver2,Ramoni Rachel B3,Morley Debra S4,Joffe Steven56,Plon Sharon E7

Affiliation:

1. Center for Medical Ethics & Health Policy, Baylor College of Medicine, Houston, TX 77030, USA.

2. Center for Medical Ethics & Health Policy, Baylor College of Medicine, Houston, TX 77030, USA

3. Center for Biomedical Informatics, Harvard Medical School, Boston, MA 02115, USA

4. Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA

5. Department of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA

6. Department of Medicine, Boston Children’s Hospital, Boston, MA 02115, USA

7. Texas Children’s Cancer Center, Department of Pediatrics, Baylor College of Medicine, Houston, TX 77030, USA

Abstract

Aim: The return of individual genetic research results has been identified as one of the most pressing ethical challenges warranting immediate policy attention. We explored the practices and perspectives of genome-wide association studies (GWAS) investigators on this topic. Materials & methods: Corresponding authors of published GWAS were invited to participate in a semistructured interview. Interviews (n = 35) were transcribed and analyzed using conventional content analysis. Results: Most investigators had not returned GWAS results. Several had experience returning results in the context of linkage/family studies, and many felt that it will become a larger issue in whole-genome/-exome sequencing. Conclusions: Research context and nature of the study are important considerations in the decision to return results. More nuanced ethical guidelines should take these contextual factors into account.

Publisher

Future Medicine Ltd

Subject

Pharmacology,Molecular Medicine,General Medicine

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