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Political economy, stakeholder voices, and saliency: lessons from international policies regulating insurer use of genetic information
A decade ago, Congress passed the Genetic Information Nondiscrimination Act (GINA), with the goals to address fear of genetic discrimination and prevent adverse health insurance and employment decisions on the basis of one's genetic information. Yet, fear of discrimination remains because other...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Oxford University Press
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6534773/ https://www.ncbi.nlm.nih.gov/pubmed/31143452 http://dx.doi.org/10.1093/jlb/lsz001 |
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author | Prince, Anya E R |
author_facet | Prince, Anya E R |
author_sort | Prince, Anya E R |
collection | PubMed |
description | A decade ago, Congress passed the Genetic Information Nondiscrimination Act (GINA), with the goals to address fear of genetic discrimination and prevent adverse health insurance and employment decisions on the basis of one's genetic information. Yet, fear of discrimination remains because other insurers, notably life, long-term care, and disability insurers, are not covered by the law. Therefore, there have been persistent murmurings for a ‘GINA 2.0’ to extend the protections of the original law. Although it is plausible to assume that the insurance industry has the political economy to control future regulation, given the saliency of genetic discrimination, other stakeholders and bureaucrats may have greater influence. This paper explores the history of policy in four countries—the United Kingdom, Sweden, Australia, and Canada. Each country provides examples of continued policy debate and change following an initial period of reliance on insurance industry self-regulation, with change generally occurring over the objection of the insurance industry. This article argues that US insurers, regulators, and stakeholders should negotiate a consensus solution for insurer use of genetic information that balances between social and economic considerations. Without compromise, continued saliency and a weakened political economy of insurers will foster continued entrenched debate on the issue. |
format | Online Article Text |
id | pubmed-6534773 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-65347732019-05-29 Political economy, stakeholder voices, and saliency: lessons from international policies regulating insurer use of genetic information Prince, Anya E R J Law Biosci Original Article A decade ago, Congress passed the Genetic Information Nondiscrimination Act (GINA), with the goals to address fear of genetic discrimination and prevent adverse health insurance and employment decisions on the basis of one's genetic information. Yet, fear of discrimination remains because other insurers, notably life, long-term care, and disability insurers, are not covered by the law. Therefore, there have been persistent murmurings for a ‘GINA 2.0’ to extend the protections of the original law. Although it is plausible to assume that the insurance industry has the political economy to control future regulation, given the saliency of genetic discrimination, other stakeholders and bureaucrats may have greater influence. This paper explores the history of policy in four countries—the United Kingdom, Sweden, Australia, and Canada. Each country provides examples of continued policy debate and change following an initial period of reliance on insurance industry self-regulation, with change generally occurring over the objection of the insurance industry. This article argues that US insurers, regulators, and stakeholders should negotiate a consensus solution for insurer use of genetic information that balances between social and economic considerations. Without compromise, continued saliency and a weakened political economy of insurers will foster continued entrenched debate on the issue. Oxford University Press 2019-05-25 /pmc/articles/PMC6534773/ /pubmed/31143452 http://dx.doi.org/10.1093/jlb/lsz001 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of Duke University School of Law, Harvard Law School, Oxford University Press, and Stanford Law School. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Original Article Prince, Anya E R Political economy, stakeholder voices, and saliency: lessons from international policies regulating insurer use of genetic information |
title | Political economy, stakeholder voices, and saliency: lessons from international policies regulating insurer use of genetic information |
title_full | Political economy, stakeholder voices, and saliency: lessons from international policies regulating insurer use of genetic information |
title_fullStr | Political economy, stakeholder voices, and saliency: lessons from international policies regulating insurer use of genetic information |
title_full_unstemmed | Political economy, stakeholder voices, and saliency: lessons from international policies regulating insurer use of genetic information |
title_short | Political economy, stakeholder voices, and saliency: lessons from international policies regulating insurer use of genetic information |
title_sort | political economy, stakeholder voices, and saliency: lessons from international policies regulating insurer use of genetic information |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6534773/ https://www.ncbi.nlm.nih.gov/pubmed/31143452 http://dx.doi.org/10.1093/jlb/lsz001 |
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