Literature DB >> 18197056

DNA data sharing: research participants' perspectives.

Amy L McGuire1, Jennifer A Hamilton, Rebecca Lunstroth, Laurence B McCullough, Alica Goldman.   

Abstract

PURPOSE: Current genomic research policy calls for public data release with specific consent for data sharing. Because most clinical investigators are not responsible for and do not anticipate data broadcast few include information about data sharing in their informed consent process. Model language is therefore urgently needed and should be responsive to research participants' attitudes and judgments. The purpose of this study was to describe research participants' attitudes and judgments about data release and their preferences for varying levels of control over decision-making.
METHODS: Focus group sessions with patients and controls from a genetic study of epilepsy.
RESULTS: Despite wide variation in judgments, there was general interest in receiving information and making decisions about data sharing. Participants preferred multiple data sharing options, but were more likely to consent to public data release when given fewer options. For existing samples most participants felt that genomic information should not be publicly released without explicit consent from research participants.
CONCLUSIONS: Specific information about data sharing ought to be included in the consent process for all genetic research. These participants desire multiple data release options, but the effect, if any, on consent to public release deserves further investigation.

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Year:  2008        PMID: 18197056      PMCID: PMC2767246          DOI: 10.1097/GIM.0b013e31815f1e00

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


  9 in total

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Authors:  Zhen Lin; Art B Owen; Russ B Altman
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2.  Genetics. No longer de-identified.

Authors:  Amy L McGuire; Richard A Gibbs
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3.  Meeting the growing demands of genetic research.

Authors:  Amy L McGuire; Richard A Gibbs
Journal:  J Law Med Ethics       Date:  2006       Impact factor: 1.718

4.  Ethical and regulatory challenges associated with the exception from informed consent requirements for emergency research: from experimental design to institutional review board approval.

Authors:  Steven N Vaslef; Charles B Cairns; John M Falletta
Journal:  Arch Surg       Date:  2006-10

Review 5.  Public willingness to participate in and public opinions about genetic variation research: a review of the literature.

Authors:  Rene Sterling; Gail E Henderson; Giselle Corbie-Smith
Journal:  Am J Public Health       Date:  2006-10-03       Impact factor: 9.308

6.  Ethics. Identifiability in genomic research.

Authors:  William W Lowrance; Francis S Collins
Journal:  Science       Date:  2007-08-03       Impact factor: 47.728

7.  New models of collaboration in genome-wide association studies: the Genetic Association Information Network.

Authors:  Teri A Manolio; Laura Lyman Rodriguez; Lisa Brooks; Gonçalo Abecasis; Dennis Ballinger; Mark Daly; Peter Donnelly; Stephen V Faraone; Kelly Frazer; Stacey Gabriel; Pablo Gejman; Alan Guttmacher; Emily L Harris; Thomas Insel; John R Kelsoe; Eric Lander; Norma McCowin; Matthew D Mailman; Elizabeth Nabel; James Ostell; Elizabeth Pugh; Stephen Sherry; Patrick F Sullivan; John F Thompson; James Warram; David Wholley; Patrice M Milos; Francis S Collins
Journal:  Nat Genet       Date:  2007-09       Impact factor: 38.330

8.  What role do patients wish to play in treatment decision making?

Authors:  R B Deber; N Kraetschmer; J Irvine
Journal:  Arch Intern Med       Date:  1996-07-08

9.  A typology of preferences for participation in healthcare decision making.

Authors:  Kathryn E Flynn; Maureen A Smith; David Vanness
Journal:  Soc Sci Med       Date:  2006-05-11       Impact factor: 4.634

  9 in total
  50 in total

Review 1.  The tension between data sharing and the protection of privacy in genomics research.

Authors:  Jane Kaye
Journal:  Annu Rev Genomics Hum Genet       Date:  2012-03-09       Impact factor: 8.929

2.  Biobank Recruitment: Motivations for Nonparticipation.

Authors:  Katrina A B Goddard; K Sabina Smith; Chuhe Chen; Carmit McMullen; Cheryl Johnson
Journal:  Biopreserv Biobank       Date:  2009-06       Impact factor: 2.300

3.  Considerations in the construction of an instrument to assess attitudes regarding critical illness gene variation research.

Authors:  Bradley D Freeman; Carie R Kennedy; Dragana Bolcic-Jankovic; Alexander Eastman; Ellen Iverson; Erica Shehane; Aaron Celious; Jennifer Barillas; Brian Clarridge
Journal:  J Empir Res Hum Res Ethics       Date:  2012-02       Impact factor: 1.742

4.  Informed consent for whole genome sequencing: a qualitative analysis of participant expectations and perceptions of risks, benefits, and harms.

Authors:  Holly K Tabor; Jacquie Stock; Tracy Brazg; Margaret J McMillin; Karin M Dent; Joon-Ho Yu; Jay Shendure; Michael J Bamshad
Journal:  Am J Med Genet A       Date:  2012-04-24       Impact factor: 2.802

Review 5.  Informed consent in genomics and genetic research.

Authors:  Amy L McGuire; Laura M Beskow
Journal:  Annu Rev Genomics Hum Genet       Date:  2010       Impact factor: 8.929

6.  Public Attitudes toward Consent and Data Sharing in Biobank Research: A Large Multi-site Experimental Survey in the US.

Authors:  Saskia C Sanderson; Kyle B Brothers; Nathaniel D Mercaldo; Ellen Wright Clayton; Armand H Matheny Antommaria; Sharon A Aufox; Murray H Brilliant; Diego Campos; David S Carrell; John Connolly; Pat Conway; Stephanie M Fullerton; Nanibaa' A Garrison; Carol R Horowitz; Gail P Jarvik; David Kaufman; Terrie E Kitchner; Rongling Li; Evette J Ludman; Catherine A McCarty; Jennifer B McCormick; Valerie D McManus; Melanie F Myers; Aaron Scrol; Janet L Williams; Martha J Shrubsole; Jonathan S Schildcrout; Maureen E Smith; Ingrid A Holm
Journal:  Am J Hum Genet       Date:  2017-02-09       Impact factor: 11.025

7.  Demographic differences in willingness to provide broad and narrow consent for biobank research.

Authors:  Altovise T Ewing; Lori A H Erby; Juli Bollinger; Eva Tetteyfio; Luisel J Ricks-Santi; David Kaufman
Journal:  Biopreserv Biobank       Date:  2015-03-31       Impact factor: 2.300

Review 8.  Identifiability in biobanks: models, measures, and mitigation strategies.

Authors:  Bradley Malin; Grigorios Loukides; Kathleen Benitez; Ellen Wright Clayton
Journal:  Hum Genet       Date:  2011-07-08       Impact factor: 4.132

9.  Perspectives of Decisional Surrogates and Patients Regarding Critical Illness Genetic Research.

Authors:  Bradley D Freeman; Dragana Bolcic-Jankovic; Carie R Kennedy; Jessica LeBlanc; Alexander Eastman; Jennifer Barillas; Catherine M Wittgen; Kathryn Indsey; Rumel S Mahmood; Brian R Clarridge
Journal:  AJOB Empir Bioeth       Date:  2015-05-01

10.  Informed Consent in Genome-Scale Research: What Do Prospective Participants Think?

Authors:  Susan Brown Trinidad; Stephanie M Fullerton; Julie M Bares; Gail P Jarvik; Eric B Larson; Wylie Burke
Journal:  AJOB Prim Res       Date:  2012-06-19
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