Literature DB >> 22402755

Public preferences regarding the return of individual genetic research results: findings from a qualitative focus group study.

Juli Murphy Bollinger1, Joan Scott, Rachel Dvoskin, David Kaufman.   

Abstract

PURPOSE: People are interested in receiving their individual research results in exchange for participating in genetic research. However, it is unclear whether the public understands the nature and limitations of these results and whether they would want information with unknown clinical utility.
METHODS: We conducted 10 focus groups in three US cities to examine the types of results people would want and the perceived value of different types of individual research results.
RESULTS: Nearly all focus group participants said they would want at least some individual research results returned. Priority was placed on results that are well understood. Less important to participants were the magnitude of the risk conferred and actionability of the result. In addition to helping treat or prevent disease, participants identified several other potential health-related and personal reasons for wanting individual research results. Many believed that researchers have an obligation to return individual research results. Although most people would prefer to receive as much information as possible, many would accept the return of a limited set of results.
CONCLUSION: Participants understood the nuances and limitations of individual research results. Researchers deciding the value of returning a given result should consider using a broader definition of clinical utility as well as the possible personal utility of the information.

Entities:  

Mesh:

Year:  2012        PMID: 22402755      PMCID: PMC3927946          DOI: 10.1038/gim.2011.66

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


  25 in total

1.  The debate over research on stored biological samples: what do sources think?

Authors:  Dave Wendler; Ezekiel Emanuel
Journal:  Arch Intern Med       Date:  2002-07-08

2.  Disclosing individual results of clinical research: implications of respect for participants.

Authors:  David I Shalowitz; Franklin G Miller
Journal:  JAMA       Date:  2005-08-10       Impact factor: 56.272

3.  Implications of disclosing individual results of clinical research.

Authors:  Ellen Wright Clayton; Lainie Friedman Ross
Journal:  JAMA       Date:  2006-01-04       Impact factor: 56.272

4.  Taking our obligations to research participants seriously: disclosing individual results of genetic research.

Authors:  Teri A Manolio
Journal:  Am J Bioeth       Date:  2006 Nov-Dec       Impact factor: 11.229

5.  Questions, complexities, and limitations in disclosing individual genetic results.

Authors:  Robert Klitzman
Journal:  Am J Bioeth       Date:  2006 Nov-Dec       Impact factor: 11.229

6.  Clinical utility and full disclosure of genetic results to research participants.

Authors:  Richard R Sharp; Morris W Foster
Journal:  Am J Bioeth       Date:  2006 Nov-Dec       Impact factor: 11.229

Review 7.  Research ethics and the challenge of whole-genome sequencing.

Authors:  Amy L McGuire; Timothy Caulfield; Mildred K Cho
Journal:  Nat Rev Genet       Date:  2008-02       Impact factor: 53.242

Review 8.  Population biobanks and returning individual research results: mission impossible or new directions?

Authors:  Susan E Wallace; Alastair Kent
Journal:  Hum Genet       Date:  2011-06-05       Impact factor: 4.132

9.  Communication of biobanks' research results: what do (potential) participants want?

Authors:  Tineke M Meulenkamp; Sjef K Gevers; Jasper A Bovenberg; Gerard H Koppelman; Astrid van Hylckama Vlieg; Ellen M A Smets
Journal:  Am J Med Genet A       Date:  2010-10       Impact factor: 2.802

10.  Subjects matter: a survey of public opinions about a large genetic cohort study.

Authors:  David Kaufman; Juli Murphy; Joan Scott; Kathy Hudson
Journal:  Genet Med       Date:  2008-11       Impact factor: 8.822

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  112 in total

1.  Preferences Regarding Return of Genomic Results to Relatives of Research Participants, Including after Participant Death: Empirical Results from a Cancer Biobank.

Authors:  Carmen Radecki Breitkopf; Gloria M Petersen; Susan M Wolf; Kari G Chaffee; Marguerite E Robinson; Deborah R Gordon; Noralane M Lindor; Barbara A Koenig
Journal:  J Law Med Ethics       Date:  2015       Impact factor: 1.718

2.  Returning a Research Participant's Genomic Results to Relatives: Analysis and Recommendations.

Authors:  Susan M Wolf; Rebecca Branum; Barbara A Koenig; Gloria M Petersen; Susan A Berry; Laura M Beskow; Mary B Daly; Conrad V Fernandez; Robert C Green; Bonnie S LeRoy; Noralane M Lindor; P Pearl O'Rourke; Carmen Radecki Breitkopf; Mark A Rothstein; Brian Van Ness; Benjamin S Wilfond
Journal:  J Law Med Ethics       Date:  2015       Impact factor: 1.718

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

Authors:  Anya E R Prince; John M Conley; Arlene M Davis; Gabriel Lázaro-Muñoz; R Jean Cadigan
Journal:  J Law Med Ethics       Date:  2015       Impact factor: 1.718

Review 4.  Return of individual research results and incidental findings: facing the challenges of translational science.

Authors:  Susan M Wolf
Journal:  Annu Rev Genomics Hum Genet       Date:  2013-07-15       Impact factor: 8.929

Review 5.  Incidental findings from clinical genome-wide sequencing: a review.

Authors:  Z Lohn; S Adam; P H Birch; J M Friedman
Journal:  J Genet Couns       Date:  2013-05-26       Impact factor: 2.537

6.  Impact of behavioral genetic evidence on the perceptions and dispositions of child abuse victims.

Authors:  Raymond Raad; Paul S Appelbaum
Journal:  Public Health Genomics       Date:  2014-07-22       Impact factor: 2.000

7.  Perceptions regarding genetic testing in populations at risk for nephropathy.

Authors:  Barry I Freedman; Alison J Fletcher; Vivek R Sanghani; Mitzie Spainhour; Angelina W Graham; Gregory B Russell; Jessica N Cooke Bailey; Ana S Iltis; Nancy M P King
Journal:  Am J Nephrol       Date:  2013-11-21       Impact factor: 3.754

8.  Disclosure of genetic research results to members of a founder population.

Authors:  Rebecca L Anderson; Kathleen Murray; Jessica X Chong; Rebecca Ouwenga; Marina Antillon; Peixian Chen; Lorena Diaz de Leon; Kathryn J Swoboda; Lucille A Lester; Soma Das; Carole Ober; Darrel J Waggoner
Journal:  J Genet Couns       Date:  2014-04-29       Impact factor: 2.537

Review 9.  Evolving approaches to the ethical management of genomic data.

Authors:  Jean E McEwen; Joy T Boyer; Kathie Y Sun
Journal:  Trends Genet       Date:  2013-02-28       Impact factor: 11.639

10.  Genetics specialists' perspectives on disclosure of genomic incidental findings in the clinical setting.

Authors:  Nancy R Downing; Janet K Williams; Sandra Daack-Hirsch; Martha Driessnack; Christian M Simon
Journal:  Patient Educ Couns       Date:  2012-10-12
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