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Genomics and insurance in the United Kingdom: increasing complexity and emerging challenges.
Dixon, Padraig; Horton, Rachel H; Newman, William G; McDermott, John H; Lucassen, Anneke.
Afiliação
  • Dixon P; Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK.
  • Horton RH; Centre for Personalised Medicine, University of Oxford, Oxford, UK.
  • Newman WG; Centre for Personalised Medicine, University of Oxford, Oxford, UK.
  • McDermott JH; Clinical Ethics, Law and Society research group, Wellcome Centre for Human Genetics, University of Oxford, Oxford, UK.
  • Lucassen A; Evolution, Infection and Genomics, School of Biological Sciences, University of Manchester, Manchester, UK.
Health Econ Policy Law ; : 1-13, 2024 May 16.
Article em En | MEDLINE | ID: mdl-38752549
ABSTRACT
This article identifies issues relating to the use of genetics and genomics in risk-rated insurance that may challenge existing regulatory models in the UK and elsewhere. We discuss three core issues (1) As genomic testing advances, and results are increasingly relevant to guide healthcare across an individual's lifetime, the distinction between diagnostic and predictive testing that the current UK insurance code relies on becomes increasingly blurred. (2) The emerging category of pharmacogenetic tests that are predictive only in the context of a specific prescribing moment. (3) The increasing availability and affordability of polygenic scores that are neither clearly diagnostic nor highly predictive, but which nonetheless might have incremental value for risk-rated insurance underwriting beyond conventional factors. We suggest a deliberative approach is required to establish when and how genetic information can be used in risk-rated insurance.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article