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Intentions to receive individual results from whole-genome sequencing among participants in the ClinSeq study : European Journal of Human Genetics
Abstract
"Genome
sequencing has been rapidly integrated into clinical research and is
currently marketed to health-care practitioners and consumers alike. The
volume of sequencing data generated for a single individual and the
wide range of findings from whole-genome sequencing raise critical
questions about the return of results and their potential value for
end-users. We conducted a mixed-methods study of 311 sequential
participants in the NIH ClinSeq study to assess general preferences and
specific attitudes toward learning results. We tested how these
variables predicted intentions to receive results within four categories
of findings ranging from medically actionable to variants of unknown
significance. Two hundred and ninety-four participants indicated a
preference to learn their genome sequencing results. Most often,
participants cited disease prevention as their reason, including
intention to change their lifestyle behaviors. Participants held
positive attitudes, strongly perceived social norms and strong
intentions to learn results, although there were significant mean
differences among four categories of findings (P<0.01). Attitudes and
social norms for medically actionable and carrier results were most
similar and rated the highest. Participants distinguished among the
types and quality of information they may receive, despite strong
intentions to learn all results presented. These intentions were
motivated by confidence in their ability to use the information to
prevent future disease and a belief in the value of even uninterpretable
information. It behooves investigators to facilitate participants’
desire to learn a range of information from genomic sequencing while
promoting realistic expectations for its clinical and personal utility."
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