Polygenic risk scores for the prediction of cardiometabolic disease

Author:

O’Sullivan Jack W12ORCID,Ashley Euan A123ORCID,Elliott Perry M45ORCID

Affiliation:

1. Stanford Center for Inherited Cardiovascular Disease, Stanford University School of Medicine , Stanford, CA , USA

2. Division of Cardiology, Department of Medicine, Stanford University School of Medicine , Stanford, CA , USA

3. Department of Genetics, Stanford University School of Medicine , Stanford, CA , USA

4. UCL Institute of Cardiovascular Science , Gower Street, London WC1E 6BT , UK

5. St. Bartholomew's Hospital , W Smithfield, London EC1A 7BE , UK

Abstract

Abstract Cardiometabolic diseases contribute more to global morbidity and mortality than any other group of disorders. Polygenic risk scores (PRSs), the weighted summation of individually small-effect genetic variants, represent an advance in our ability to predict the development and complications of cardiometabolic diseases. This article reviews the evidence supporting the use of PRS in seven common cardiometabolic diseases: coronary artery disease (CAD), stroke, hypertension, heart failure and cardiomyopathies, obesity, atrial fibrillation (AF), and type 2 diabetes mellitus (T2DM). Data suggest that PRS for CAD, AF, and T2DM consistently improves prediction when incorporated into existing clinical risk tools. In other areas such as ischaemic stroke and hypertension, clinical application appears premature but emerging evidence suggests that the study of larger and more diverse populations coupled with more granular phenotyping will propel the translation of PRS into practical clinical prediction tools.

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine

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