Abstract
Purpose:Whether and how to return individual genetic results to study participants is among the most contentious policy issues in contemporary genomic research.Methods:We surveyed corresponding authors of genome-wide association studies, identified through the National Human Genome Research Institute's Catalog of Published Genome-Wide Association Studies, to describe the experiences and attitudes of these stakeholders.Results:Of 357 corresponding authors, 200 (56%) responded. One hundred twenty-six (63%) had been responsible for primary data and sample collection, whereas 74 (37%) had performed secondary analyses. Only 7 (4%) had returned individual results within their index genome-wide association studies. Most (69%) believed that return of results to individual participants was warranted under at least some circumstances. Most respondents identified a desire to benefit participants' health (63%) and respect for participants' desire for information (57%) as major motivations for returning results. Most also identified uncertain clinical utility (76%), the possibility that participants will misunderstand results (74%), the potential for emotional harm (61%), the need to ensure access to trained clinicians (59%), and the potential for loss of confidentiality (51%) as major barriers to return of results.Conclusion:Investigators have limited experience returning individual results from genome-scale research, yet most are motivated to do so in at least some circumstances.
Original language | English (US) |
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Pages (from-to) | 882-887 |
Number of pages | 6 |
Journal | Genetics in Medicine |
Volume | 15 |
Issue number | 11 |
DOIs | |
State | Published - Nov 2013 |
Keywords
- incidental findings
- return of results
ASJC Scopus subject areas
- Genetics(clinical)