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A systematic literature review of individuals’ perspectives on privacy and genetic information in the United States

Concerns about genetic privacy affect individuals’ willingness to accept genetic testing in clinical care and to participate in genomics research. To learn what is already known about these views, we conducted a systematic review, which ultimately analyzed 53 studies involving the perspectives of 47...

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Detalles Bibliográficos
Autores principales: Clayton, Ellen W., Halverson, Colin M., Sathe, Nila A., Malin, Bradley A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6209148/
https://www.ncbi.nlm.nih.gov/pubmed/30379944
http://dx.doi.org/10.1371/journal.pone.0204417
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author Clayton, Ellen W.
Halverson, Colin M.
Sathe, Nila A.
Malin, Bradley A.
author_facet Clayton, Ellen W.
Halverson, Colin M.
Sathe, Nila A.
Malin, Bradley A.
author_sort Clayton, Ellen W.
collection PubMed
description Concerns about genetic privacy affect individuals’ willingness to accept genetic testing in clinical care and to participate in genomics research. To learn what is already known about these views, we conducted a systematic review, which ultimately analyzed 53 studies involving the perspectives of 47,974 participants on real or hypothetical privacy issues related to human genetic data. Bibliographic databases included MEDLINE, Web of Knowledge, and Sociological Abstracts. Three investigators independently screened studies against predetermined criteria and assessed risk of bias. The picture of genetic privacy that emerges from this systematic literature review is complex and riddled with gaps. When asked specifically “are you worried about genetic privacy,” the general public, patients, and professionals frequently said yes. In many cases, however, that question was posed poorly or only in the most general terms. While many participants expressed concern that genomic and medical information would be revealed to others, respondents frequently seemed to conflate privacy, confidentiality, control, and security. People varied widely in how much control they wanted over the use of data. They were more concerned about use by employers, insurers, and the government than they were about researchers and commercial entities. In addition, people are often willing to give up some privacy to obtain other goods. Importantly, little attention was paid to understanding the factors–sociocultural, relational, and media—that influence people’s opinions and decisions. Future investigations should explore in greater depth which concerns about genetic privacy are most salient to people and the social forces and contexts that influence those perceptions. It is also critical to identify the social practices that will make the collection and use of these data more trustworthy for participants as well as to identify the circumstances that lead people to set aside worries and decide to participate in research.
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spelling pubmed-62091482018-11-19 A systematic literature review of individuals’ perspectives on privacy and genetic information in the United States Clayton, Ellen W. Halverson, Colin M. Sathe, Nila A. Malin, Bradley A. PLoS One Research Article Concerns about genetic privacy affect individuals’ willingness to accept genetic testing in clinical care and to participate in genomics research. To learn what is already known about these views, we conducted a systematic review, which ultimately analyzed 53 studies involving the perspectives of 47,974 participants on real or hypothetical privacy issues related to human genetic data. Bibliographic databases included MEDLINE, Web of Knowledge, and Sociological Abstracts. Three investigators independently screened studies against predetermined criteria and assessed risk of bias. The picture of genetic privacy that emerges from this systematic literature review is complex and riddled with gaps. When asked specifically “are you worried about genetic privacy,” the general public, patients, and professionals frequently said yes. In many cases, however, that question was posed poorly or only in the most general terms. While many participants expressed concern that genomic and medical information would be revealed to others, respondents frequently seemed to conflate privacy, confidentiality, control, and security. People varied widely in how much control they wanted over the use of data. They were more concerned about use by employers, insurers, and the government than they were about researchers and commercial entities. In addition, people are often willing to give up some privacy to obtain other goods. Importantly, little attention was paid to understanding the factors–sociocultural, relational, and media—that influence people’s opinions and decisions. Future investigations should explore in greater depth which concerns about genetic privacy are most salient to people and the social forces and contexts that influence those perceptions. It is also critical to identify the social practices that will make the collection and use of these data more trustworthy for participants as well as to identify the circumstances that lead people to set aside worries and decide to participate in research. Public Library of Science 2018-10-31 /pmc/articles/PMC6209148/ /pubmed/30379944 http://dx.doi.org/10.1371/journal.pone.0204417 Text en © 2018 Clayton et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Clayton, Ellen W.
Halverson, Colin M.
Sathe, Nila A.
Malin, Bradley A.
A systematic literature review of individuals’ perspectives on privacy and genetic information in the United States
title A systematic literature review of individuals’ perspectives on privacy and genetic information in the United States
title_full A systematic literature review of individuals’ perspectives on privacy and genetic information in the United States
title_fullStr A systematic literature review of individuals’ perspectives on privacy and genetic information in the United States
title_full_unstemmed A systematic literature review of individuals’ perspectives on privacy and genetic information in the United States
title_short A systematic literature review of individuals’ perspectives on privacy and genetic information in the United States
title_sort systematic literature review of individuals’ perspectives on privacy and genetic information in the united states
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6209148/
https://www.ncbi.nlm.nih.gov/pubmed/30379944
http://dx.doi.org/10.1371/journal.pone.0204417
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