4.0 Article

Motivations and Perceptions of Early Adopters of Personalized Genomics: Perspectives from Research Participants

Journal

PUBLIC HEALTH GENOMICS
Volume 15, Issue 1, Pages 22-30

Publisher

KARGER
DOI: 10.1159/000327296

Keywords

Commercialization; Consumer views; Genetic tests; Direct-to-consumer; Personalized medicine; Public expectations; Survey research

Funding

  1. National Human Genome Research Institute, National Institutes of Health [1RC1HG005369-01, 1-P50HG004487-01]
  2. William G. Rohrer Foundation
  3. RNR Foundation
  4. Robert Wood Johnson Foundation Health Society
  5. NATIONAL HUMAN GENOME RESEARCH INSTITUTE [RC1HG005369, P50HG004487] Funding Source: NIH RePORTER

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Background/Aims: To predict the potential public health impact of personal genomics, empirical research on public perceptions of these services is needed. In this study, 'early adopters' of personal genomics were surveyed to assess their motivations, perceptions and intentions. Methods: Participants were recruited from everyone who registered to attend an enrollment event for the Coriell Personalized Medicine Collaborative, a United States-based (Camden, N.J.) research study of the utility of personalized medicine, between March 31, 2009 and April 1, 2010 (n = 369). Participants completed an Internet-based survey about their motivations, awareness of personalized medicine, perceptions of study risks and benefits, and intentions to share results with health care providers. Results: Respondents were motivated to participate for their own curiosity and to find out their disease risk to improve their health. Fewer than 10% expressed deterministic perspectives about genetic risk, but 32% had misperceptions about the research study or personal genomic testing. Most respondents perceived the study to have health-related benefits. Nearly all (92%) intended to share their results with physicians, primarily to request specific medical recommendations. Conclusion: Early adopters of personal genomics are prospectively enthusiastic about using genomic profiling information to improve their health, in close consultation with their physicians. This suggests that early users (i.e. through direct-to-consumer companies or research) may follow up with the health care system. Further research should address whether intentions to seek care match actual behaviors. Copyright (C) 2011 S. Karger AG, Basel

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