Literature DB >> 22241102

Genetics researchers' and IRB professionals' attitudes toward genetic research review: a comparative analysis.

Karen L Edwards1, Amy A Lemke, Susan B Trinidad, Susan M Lewis, Helene Starks, Katherine W Snapinn, Mary Quinn Griffin, Georgia L Wiesner, Wylie Burke.   

Abstract

PURPOSE: Genetic research involving human participants can pose challenging questions related to ethical and regulatory standards for research oversight. However, few empirical studies describe how genetic researchers and institutional review board (IRB) professionals conceptualize ethical issues in genetic research or where common ground might exist.
METHODS: Parallel online surveys collected information from human genetic researchers (n = 351) and IRB professionals (n = 208) regarding their views about human participant oversight for genetic protocols.
RESULTS: A range of opinions were observed within groups on most issues. In both groups, a minority thought it likely that people would be harmed by participation in genetic research or identified from coded genetic data. A majority of both groups agreed that reconsent should be required for four of the six scenarios presented. Statistically significant differences were observed between groups on some issues, with more genetic researcher respondents trusting the confidentiality of coded data, fewer expecting harms from reidentification, and fewer considering reconsent necessary in certain scenarios.
CONCLUSION: The range of views observed within and between IRB and genetic researcher groups highlights the complexity and unsettled nature of many ethical issues in genome research. Our findings also identify areas where researcher and IRB views diverge and areas of common ground.

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Year:  2012        PMID: 22241102      PMCID: PMC3448270          DOI: 10.1038/gim.2011.57

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


  20 in total

1.  Genetics. Genomic research and human subject privacy.

Authors:  Zhen Lin; Art B Owen; Russ B Altman
Journal:  Science       Date:  2004-07-09       Impact factor: 47.728

2.  Genetics. No longer de-identified.

Authors:  Amy L McGuire; Richard A Gibbs
Journal:  Science       Date:  2006-04-21       Impact factor: 47.728

3.  Development of a large-scale de-identified DNA biobank to enable personalized medicine.

Authors:  D M Roden; J M Pulley; M A Basford; G R Bernard; E W Clayton; J R Balser; D R Masys
Journal:  Clin Pharmacol Ther       Date:  2008-05-21       Impact factor: 6.875

4.  Attitudes toward genetic research review: results from a survey of human genetics researchers.

Authors:  K L Edwards; A A Lemke; S B Trinidad; S M Lewis; H Starks; M T Quinn Griffin; G L Wiesner
Journal:  Public Health Genomics       Date:  2011-04-11       Impact factor: 2.000

5.  Is deidentification sufficient to protect health privacy in research?

Authors:  Mark A Rothstein
Journal:  Am J Bioeth       Date:  2010-09       Impact factor: 11.229

6.  Glad you asked: participants' opinions of re-consent for dbGap data submission.

Authors:  Evette J Ludman; Stephanie M Fullerton; Leslie Spangler; Susan Brown Trinidad; Monica M Fujii; Gail P Jarvik; Eric B Larson; Wylie Burke
Journal:  J Empir Res Hum Res Ethics       Date:  2010-09       Impact factor: 1.742

7.  Public and biobank participant attitudes toward genetic research participation and data sharing.

Authors:  A A Lemke; W A Wolf; J Hebert-Beirne; M E Smith
Journal:  Public Health Genomics       Date:  2010-01-15       Impact factor: 2.000

8.  The Belmont Report. Ethical principles and guidelines for the protection of human subjects of research.

Authors: 
Journal:  J Am Coll Dent       Date:  2014

9.  Genomic research and wide data sharing: views of prospective participants.

Authors:  Susan Brown Trinidad; Stephanie M Fullerton; Julie M Bares; Gail P Jarvik; Eric B Larson; Wylie Burke
Journal:  Genet Med       Date:  2010-08       Impact factor: 8.822

Review 10.  The ethical use of existing samples for genome research.

Authors:  Oliver F Bathe; Amy L McGuire
Journal:  Genet Med       Date:  2009-10       Impact factor: 8.822

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  20 in total

1.  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

2.  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

3.  Return of results: ethical and legal distinctions between research and clinical care.

Authors:  Wylie Burke; Barbara J Evans; Gail P Jarvik
Journal:  Am J Med Genet C Semin Med Genet       Date:  2014-03-10       Impact factor: 3.908

4.  Perceptions of African-American health professionals and community members on the participation of children and pregnant women in genetic research.

Authors:  E M Ngui; T D Warner; L W Roberts
Journal:  Public Health Genomics       Date:  2013-11-06       Impact factor: 2.000

5.  Perspectives of psychiatric investigators and IRB chairs regarding benefits of psychiatric genetics research.

Authors:  Laura Weiss Roberts; Laura B Dunn; Jane Paik Kim; Maryam Rostami
Journal:  J Psychiatr Res       Date:  2018-09-15       Impact factor: 4.791

6.  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

Review 7.  Genetic research on biospecimens poses minimal risk.

Authors:  David S Wendler; Annette Rid
Journal:  Trends Genet       Date:  2014-12-16       Impact factor: 11.639

8.  Participant views on consent in cancer genetics research: preparing for the precision medicine era.

Authors:  Karen L Edwards; Diane M Korngiebel; Lesley Pfeifer; Deborah Goodman; Anne Renz; Lari Wenzel; Deborah J Bowen; Celeste M Condit
Journal:  J Community Genet       Date:  2016-01-22

9.  A comparison of views regarding the use of de-identified data.

Authors:  Deborah Goodman; Catherine O Johnson; Deborah Bowen; Megan Smith; Lari Wenzel; Karen L Edwards
Journal:  Transl Behav Med       Date:  2018-01-29       Impact factor: 3.046

10.  Consent Issues in Genetic Research: Views of Research Participants.

Authors:  Deborah Goodman; Catherine O Johnson; Lari Wenzel; Deborah Bowen; Celeste Condit; Karen L Edwards
Journal:  Public Health Genomics       Date:  2016-07-05       Impact factor: 2.000

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