Genetics of Atrial Fibrillation in 2020

Author:

Roselli Carolina12ORCID,Rienstra Michiel2ORCID,Ellinor Patrick T.13ORCID

Affiliation:

1. From the Cardiovascular Disease Initiative, Broad Institute of MIT and Harvard, Cambridge, MA (C.R., P.T.E.)

2. Department of Cardiology, University of Groningen, University Medical Center Groningen, the Netherlands (C.R., M.R.)

3. Cardiovascular Research Center and Cardiac Arrhythmia Service, Massachusetts General Hospital, Boston (P.T.E.).

Abstract

Atrial fibrillation is a common heart rhythm disorder that leads to an increased risk for stroke and heart failure. Atrial fibrillation is a complex disease with both environmental and genetic risk factors that contribute to the arrhythmia. Over the last decade, rapid progress has been made in identifying the genetic basis for this common condition. In this review, we provide an overview of the primary types of genetic analyses performed for atrial fibrillation, including linkage studies, genome-wide association studies, and studies of rare coding variation. With these results in mind, we aim to highlighting the existing knowledge gaps and future directions for atrial fibrillation genetics research.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine,Physiology

Reference88 articles.

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