Perspective: The Clinical Use of Polygenic Risk Scores: Race, Ethnicity, and Health Disparities.

Genome-Wide Association Studies Polygenic Risk Scores Precision Medicine

Journal

Ethnicity & disease
ISSN: 1945-0826
Titre abrégé: Ethn Dis
Pays: United States
ID NLM: 9109034

Informations de publication

Date de publication:
2019
Historique:
entrez: 2 8 2019
pubmed: 2 8 2019
medline: 2 8 2019
Statut: epublish

Résumé

Polygenic risk scores (PRS) are an emerging precision medicine tool based on multiple gene variants that, taken alone, have weak associations with disease risks, but collectively may enhance disease predictive value in the population. However, the benefit of PRS may not be equal among non-European populations, as they are under-represented in genome-wide association studies (GWAS) that serve as the basis for PRS development. In this perspective, we discuss a path forward, which includes: 1) inclusion of underrepresented populations in PRS research; 2) global efforts to build capacity for genomic research; 3) equitable implementation of these tools in clinical practice; and 4) traditional public health approaches to reduce risk of adverse health outcomes as an important component to precision health. As precision medicine is implemented in clinical care, researchers must ensure that advances from PRS research will benefit all.

Identifiants

pubmed: 31367172
doi: 10.18865/ed.29.3.513
pii: ed.29.3.513
pmc: PMC6645721
doi:

Types de publication

Editorial

Langues

eng

Sous-ensembles de citation

IM

Pagination

513-516

Déclaration de conflit d'intérêts

Competing Interests: None declared.

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Auteurs

Megan C Roberts (MC)

Eshelman School of Pharmacy at University of North Carolina, Chapel Hill, NC.

Muin J Khoury (MJ)

Office of Public Health Genomics, Centers for Disease Control and Prevention, Atlanta, GA.

George A Mensah (GA)

Center for Translation Research and Implementation Science, National Heart, Lung, and Blood Institute, Bethesda, MD.

Classifications MeSH