Literature DB >> 22213783

Balancing the risks and benefits of genomic data sharing: genome research participants' perspectives.

J M Oliver1, M J Slashinski, T Wang, P A Kelly, S G Hilsenbeck, A L McGuire.   

Abstract

BACKGROUND: Technological advancements are rapidly propelling the field of genome research forward, while lawmakers attempt to keep apace with the risks these advances bear. Balancing normative concerns of maximizing data utility and protecting human subjects, whose privacy is at risk due to the identifiability of DNA data, are central to policy decisions. Research on genome research participants making real-time data sharing decisions is limited; yet, these perspectives could provide critical information to ongoing deliberations.
METHODS: We conducted a randomized trial of 3 consent types affording varying levels of control over data release decisions. After debriefing participants about the randomization process, we invited them to a follow-up interview to assess their attitudes toward genetic research, privacy and data sharing.
RESULTS: Participants were more restrictive in their reported data sharing preferences than in their actual data sharing decisions. They saw both benefits and risks associated with sharing their genomic data, but risks were seen as less concrete or happening in the future, and were largely outweighed by purported benefits.
CONCLUSION: Policymakers must respect that participants' assessment of the risks and benefits of data sharing and their privacy-utility determinations, which are associated with their final data release decisions, vary. In order to advance the ethical conduct of genome research, proposed policy changes should carefully consider these stakeholder perspectives.
Copyright © 2011 S. Karger AG, Basel.

Entities:  

Mesh:

Year:  2011        PMID: 22213783      PMCID: PMC3318928          DOI: 10.1159/000334718

Source DB:  PubMed          Journal:  Public Health Genomics        ISSN: 1662-4246            Impact factor:   2.000


  23 in total

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Authors: 
Journal:  Code Fed Regul Public Welfare       Date:  1995-10-01

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5.  Genetics. No longer de-identified.

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  48 in total

Review 1.  Privacy challenges and research opportunities for genomic data sharing.

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2.  EngageUC: Developing an Efficient and Ethical Approach to Biobanking Research at the University of California.

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3.  Authorization of tissues from deceased patients for genetic research.

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4.  One Size Doesn't Fit All: Measuring Individual Privacy in Aggregate Genomic Data.

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5.  Pediatric data sharing in genomic research: attitudes and preferences of parents.

Authors:  Matthew D Burstein; Jill Oliver Robinson; Susan G Hilsenbeck; Amy L McGuire; Ching C Lau
Journal:  Pediatrics       Date:  2014-03-10       Impact factor: 7.124

6.  Clinical Trial Participants' Views of the Risks and Benefits of Data Sharing.

Authors:  Michelle M Mello; Van Lieou; Steven N Goodman
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7.  Big Data Privacy in Biomedical Research.

Authors:  Shuang Wang; Luca Bonomi; Wenrui Dai; Feng Chen; Cynthia Cheung; Cinnamon S Bloss; Samuel Cheng; Xiaoqian Jiang
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Review 8.  Evolving approaches to the ethical management of genomic data.

Authors:  Jean E McEwen; Joy T Boyer; Kathie Y Sun
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10.  Practices and policies of clinical exome sequencing providers: analysis and implications.

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