Psychiatric genetics researchers' views on offering return of results to individual participants
- 25 October 2018
- journal article
- research article
- Published by Wiley in American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
- Vol. 180 (8) , 589-600
Abstract
In the middle of growing consensus that genomics researchers should offer to return clinically valid, medically relevant, and medically actionable findings identified in the course of research, psychiatric genetics researchers face new challenges. As they uncover the genetic architecture of psychiatric disorders through genome‐wide association studies and integrate whole genome and whole exome sequencing to their research, there is a pressing need for examining these researchers' views regarding the return of results (RoR) and the unique challenges for offering RoR from psychiatric genetics research. Based on qualitative interviews with 39 psychiatric genetics researchers from different countries operating at the forefront of their field, we provide an insider's view of researchers' practices regarding RoR and the most contentious issues in psychiatry researchers' decision‐making around RoR, including what are the strongest ethical, scientific, and practical arguments for and against offering RoR from this research. Notably, findings suggest that psychiatric genetics researchers (85%) overwhelmingly favor offering RoR of at least some findings, but only 22% of researchers are returning results. Researchers identified a number of scientific and practical concerns about RoR, and about how to return results in a responsible way to patients diagnosed with a severe psychiatric disorder. Furthermore, findings help highlight areas for further discussion and resolution of conflicts in the practice of RoR in psychiatric genetics research. As the pace of discovery in psychiatric genetics continues to surge, resolution of these uncertainties gains greater urgency to avoid ethical pitfalls and to maximize the positive impact of RoR.Keywords
Funding Information
- National Human Genome Research Institute (R00HG008689)
- National Institutes of Health
- National Human Genome Research Institute
This publication has 54 references indexed in Scilit:
- Researchers’ views on return of incidental genomic research results: qualitative and quantitative findingsGenetics in Medicine, 2013
- Ethics and neuropsychiatric genetics: a review of major issuesInternational Journal of Neuropsychopharmacology, 2012
- Five Years of GWAS DiscoveryThe American Journal of Human Genetics, 2012
- Genome-wide association study identifies five new schizophrenia lociNature Genetics, 2011
- Ethical and Practical Guidelines for Reporting Genetic Research Results to Study ParticipantsCirculation: Cardiovascular Genetics, 2010
- Researcher Perspectives on Disclosure of Incidental Findings in Genetic ResearchJournal of Empirical Research on Human Research Ethics, 2010
- Reasons for participating in randomised controlled trials: conditional altruism and considerations for selfTrials, 2010
- Disclosure ofAPOEGenotype for Risk of Alzheimer's DiseaseNew England Journal of Medicine, 2009
- Emotional distress following genetic testing for hereditary breast and ovarian cancer: A meta-analytic review.Health Psychology, 2009
- Reporting genetic results in research studies: Summary and recommendations of an NHLBI working groupAmerican Journal of Medical Genetics Part A, 2006