Literature DB >> 22241094

IRB perspectives on the return of individual results from genomic research.

Lynn G Dressler1, Sondra Smolek, Roselle Ponsaran, Janell M Markey, Helene Starks, Nancy Gerson, Susan Lewis, Nancy Press, Eric Juengst, Georgia L Wiesner.   

Abstract

PURPOSE: Return of individual research results from genomic studies is a hotly debated ethical issue in genomic research. However, the perspective of key stakeholders-institutional review board (IRB) professionals-has been missing from this dialogue. This study explores the positions and experiences of IRB members and staff regarding this issue.
METHODS: In-depth interviews with 31 IRB professionals at six sites across the United States.
RESULTS: IRB professionals agreed that research results should be returned to research participants when results are medically actionable but only if the participants want to know the results. Many respondents expected researchers to address the issue of return of results (ROR) in the IRB application and informed-consent document. Many respondents were not comfortable with their expertise in genomics research and only a few described actual experiences in addressing ROR. Although participants agreed that guidelines would be helpful, most were reticent to develop them in isolation. Even where IRB guidance exists (e.g., Clinical Laboratory Improvement Act (CLIA) lab certification required for return), in practice, the guidance has been overruled to allow ROR (e.g., no CLIA lab performs the assay).
CONCLUSION: An IRB-researcher partnership is needed to help inform responsible and feasible institutional approaches to returning research results.

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Mesh:

Year:  2012        PMID: 22241094      PMCID: PMC3493147          DOI: 10.1038/gim.2011.10

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


  28 in total

1.  Obligations in offering to disclose genetic research results.

Authors:  Conrad V Fernandez; Charles Weijer
Journal:  Am J Bioeth       Date:  2006 Nov-Dec       Impact factor: 11.229

2.  Thresholds and boundaries in the disclosure of individual genetic research results.

Authors:  Lynn G Dressler; Eric T Juengst
Journal:  Am J Bioeth       Date:  2006 Nov-Dec       Impact factor: 11.229

3.  Medicine. Reestablishing the researcher-patient compact.

Authors:  Isaac S Kohane; Kenneth D Mandl; Patrick L Taylor; Ingrid A Holm; Daniel J Nigrin; Louis M Kunkel
Journal:  Science       Date:  2007-05-11       Impact factor: 47.728

4.  Ethical issues arising from the participation of children in genetic research.

Authors:  Wylie Burke; Douglas S Diekema
Journal:  J Pediatr       Date:  2006-07       Impact factor: 4.406

5.  Attitudes toward genetic research review: results from a national survey of professionals involved in human subjects protection.

Authors:  Amy A Lemke; Susan B Trinidad; Karen L Edwards; Helene Starks; Georgia L Wiesner
Journal:  J Empir Res Hum Res Ethics       Date:  2010-03       Impact factor: 1.742

6.  The emergence of an ethical duty to disclose genetic research results: international perspectives.

Authors:  Bartha Maria Knoppers; Yann Joly; Jacques Simard; Francine Durocher
Journal:  Eur J Hum Genet       Date:  2006-07-26       Impact factor: 4.246

Review 7.  Human genome research and the public interest: progress notes from an American science policy experiment.

Authors:  E T Juengst
Journal:  Am J Hum Genet       Date:  1994-01       Impact factor: 11.025

8.  Professional integrity in clinical research.

Authors:  F G Miller; D L Rosenstein; E G DeRenzo
Journal:  JAMA       Date:  1998-10-28       Impact factor: 56.272

9.  Understanding incidental findings in the context of genetics and genomics.

Authors:  Mildred K Cho
Journal:  J Law Med Ethics       Date:  2008       Impact factor: 1.718

10.  Communicating the results of clinical research to participants: attitudes, practices, and future directions.

Authors:  David I Shalowitz; Franklin G Miller
Journal:  PLoS Med       Date:  2008-05-13       Impact factor: 11.069

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  43 in total

1.  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

2.  Pediatric Issues in Return of Results and Incidental Findings: Weighing Autonomy and Best Interests.

Authors:  Ingrid A Holm
Journal:  Genet Test Mol Biomarkers       Date:  2017-01-31

Review 3.  Disclosure of incidental findings from next-generation sequencing in pediatric genomic research.

Authors:  Ruqayyah Abdul-Karim; Benjamin E Berkman; David Wendler; Annette Rid; Javed Khan; Tom Badgett; Sara Chandros Hull
Journal:  Pediatrics       Date:  2013-02-11       Impact factor: 7.124

4.  A closer look at the recommended criteria for disclosing genetic results: perspectives of medical genetic specialists, genomic researchers, and institutional review board chairs.

Authors:  Debra S Brandt; Laura Shinkunas; Stephen L Hillis; Sandra E Daack-Hirsch; Martha Driessnack; Nancy R Downing; Megan F Liu; Lisa L Shah; Janet K Williams; Christian M Simon
Journal:  J Genet Couns       Date:  2013-04-02       Impact factor: 2.537

5.  Research participant-centered outcomes at NIH-supported clinical research centers.

Authors:  Rhonda G Kost; Laura N Lee; Jennifer L Yessis; Robert Wesley; Sandra Alfano; Steven R Alexander; Sylvia Baedorf Kassis; Philip Cola; Ann Dozier; Dan E Ford; Paul A Harris; Emmelyn Kim; Simon Craddock Lee; Gerri O'Riordan; Mary-Tara Roth; Kathryn Schuff; June Wasser; David K Henderson; Barry S Coller
Journal:  Clin Transl Sci       Date:  2014-05-19       Impact factor: 4.689

6.  Return of Genetic Research Results to Participants and Families: IRB Perspectives and Roles.

Authors:  Laura M Beskow; P Pearl O'Rourke
Journal:  J Law Med Ethics       Date:  2015       Impact factor: 1.718

7.  Genomics education for the public: perspectives of genomic researchers and ELSI advisors.

Authors:  Lynn G Dressler; Sondra Smolek Jones; Janell M Markey; Katherine W Byerly; Megan C Roberts
Journal:  Genet Test Mol Biomarkers       Date:  2014-02-04

8.  Reconceptualizing harms and benefits in the genomic age.

Authors:  Anya E R Prince; Benjamin E Berkman
Journal:  Per Med       Date:  2018-09-27       Impact factor: 2.512

Review 9.  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

10.  Merging Electronic Health Record Data and Genomics for Cardiovascular Research: A Science Advisory From the American Heart Association.

Authors:  Jennifer L Hall; John J Ryan; Bruce E Bray; Candice Brown; David Lanfear; L Kristin Newby; Mary V Relling; Neil J Risch; Dan M Roden; Stanley Y Shaw; James E Tcheng; Jessica Tenenbaum; Thomas N Wang; William S Weintraub
Journal:  Circ Cardiovasc Genet       Date:  2016-03-14
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