Literature DB >> 23807616

Researchers' views on return of incidental genomic research results: qualitative and quantitative findings.

Robert Klitzman1, Paul S Appelbaum, Abby Fyer, Josue Martinez, Brigitte Buquez, Julia Wynn, Cameron R Waldman, Jo Phelan, Erik Parens, Wendy K Chung.   

Abstract

PURPOSE: Comprehensive genomic analysis including exome and genome sequencing is increasingly being utilized in research studies, leading to the generation of incidental genetic findings. It is unclear how researchers plan to deal with incidental genetic findings.
METHODS: We conducted a survey of the practices and attitudes of 234 members of the US genetic research community and performed qualitative semistructured interviews with 28 genomic researchers to understand their views and experiences with incidental genetic research findings.
RESULTS: We found that 12% of the researchers had returned incidental genetic findings, and an additional 28% planned to do so. A large majority of researchers (95%) believe that incidental findings for highly penetrant disorders with immediate medical implications should be offered to research participants. However, there was no consensus on returning incidental results for other conditions varying in penetrance and medical actionability. Researchers raised concerns that the return of incidental findings would impose significant burdens on research and could potentially have deleterious effects on research participants if not performed well. Researchers identified assistance needed to enable effective, accurate return of incidental findings.
CONCLUSION: The majority of the researchers believe that research participants should have the option to receive at least some incidental genetic research results.

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Mesh:

Year:  2013        PMID: 23807616      PMCID: PMC3823712          DOI: 10.1038/gim.2013.87

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  19 in total

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Review 2.  Research ethics and the challenge of whole-genome sequencing.

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3.  Genomic research and incidental findings.

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4.  Secondary variants in individuals undergoing exome sequencing: screening of 572 individuals identifies high-penetrance mutations in cancer-susceptibility genes.

Authors:  Jennifer J Johnston; Wendy S Rubinstein; Flavia M Facio; David Ng; Larry N Singh; Jamie K Teer; James C Mullikin; Leslie G Biesecker
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5.  Ethical and practical guidelines for reporting genetic research results to study participants: updated guidelines from a National Heart, Lung, and Blood Institute working group.

Authors:  Richard R Fabsitz; Amy McGuire; Richard R Sharp; Mona Puggal; Laura M Beskow; Leslie G Biesecker; Ebony Bookman; Wylie Burke; Esteban Gonzalez Burchard; George Church; Ellen Wright Clayton; John H Eckfeldt; Conrad V Fernandez; Rebecca Fisher; Stephanie M Fullerton; Stacey Gabriel; Francine Gachupin; Cynthia James; Gail P Jarvik; Rick Kittles; Jennifer R Leib; Christopher O'Donnell; P Pearl O'Rourke; Laura Lyman Rodriguez; Sheri D Schully; Alan R Shuldiner; Rebecca K F Sze; Joseph V Thakuria; Susan M Wolf; Gregory L Burke
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6.  Ethical issues with genetic testing in pediatrics.

Authors: 
Journal:  Pediatrics       Date:  2001-06       Impact factor: 7.124

7.  Points to consider: ethical, legal, and psychosocial implications of genetic testing in children and adolescents. American Society of Human Genetics Board of Directors, American College of Medical Genetics Board of Directors.

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8.  High prevalence of genetic variants previously associated with LQT syndrome in new exome data.

Authors:  Lena Refsgaard; Anders G Holst; Golnaz Sadjadieh; Stig Haunsø; Jonas B Nielsen; Morten S Olesen
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9.  An informatics approach to analyzing the incidentalome.

Authors:  Jonathan S Berg; Michael Adams; Nassib Nassar; Chris Bizon; Kristy Lee; Charles P Schmitt; Kirk C Wilhelmsen; James P Evans
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10.  Subjects matter: a survey of public opinions about a large genetic cohort study.

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  66 in total

1.  Automatic Placement of Genomic Research Results in Medical Records: Do Researchers Have a Duty? Should Participants Have a Choice?

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3.  Incidental or secondary findings: an integrative and patient-inclusive approach to the current debate.

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4.  Returning a Research Participant's Genomic Results to Relatives: Perspectives from Managers of Two Distinct Research Biobanks.

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5.  Return of individual results in epilepsy genomic research: A view from the field.

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6.  Return of individual genomic research results: what do consent forms tell participants?

Authors:  Stacey Pereira; Jill Oliver Robinson; Amy L McGuire
Journal:  Eur J Hum Genet       Date:  2016-06-22       Impact factor: 4.246

Review 7.  Management and return of incidental genomic findings in clinical trials.

Authors:  C Ayuso; J M Millan; R Dal-Re
Journal:  Pharmacogenomics J       Date:  2014-10-28       Impact factor: 3.550

8.  In Different Voices: The Views of People with Disabilities about Return of Results from Precision Medicine Research.

Authors:  Maya Sabatello; Yuan Zhang; Ying Chen; Paul S Appelbaum
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9.  Psychiatric genetics researchers' views on offering return of results to individual participants.

Authors:  Kristin M Kostick; Cody Brannan; Stacey Pereira; Gabriel Lázaro-Muñoz
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2018-10-25       Impact factor: 3.568

10.  Understanding What Information Is Valued By Research Participants, And Why.

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