Genetic Determinants of Peripheral Artery Disease

Author:

Klarin Derek1234ORCID,Tsao Philip S.56ORCID,Damrauer Scott M.78ORCID

Affiliation:

1. Malcolm Randall VA Medical Center, Gainesville, FL (D.K.).

2. Division of Vascular Surgery and Endovascular Therapy, University of Florida College of Medicine, Gainesville (D.K.).

3. Center for Genomic Medicine, Massachusetts General Hospital, Harvard Medical School, Boston (D.K.).

4. Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA (D.K.).

5. VA Palo Alto Health Care System, CA (P.S.T.).

6. Division of Cardiovascular Medicine, Department of Medicine, Stanford University School of Medicine, CA (P.S.T.).

7. Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PA (S.M.D.).

8. Department of Surgery, Perlman School of Medicine, University of Pennsylvania, Philadelphia (S.M.D.).

Abstract

Peripheral artery disease—atherosclerosis of the abdominal aorta and lower extremity vascular bed—is a complex disease with both environmental and genetic determinants. Unmitigated disease is associated with major functional decline and can lead to chronic limb-threatening ischemia, amputation, and increased mortality. Over the last 10 years, major advances have been made in identifying the genetic basis of this common, complex disease. In this review, we provide an overview of the primary types of genetic analyses performed for peripheral artery disease, including heritability and linkage studies, and more recently biobank-based genome-wide association studies. Looking forward, we highlight areas of future study including efforts to identify causal peripheral artery disease genes, rare variant and structural variant analyses using whole-exome and whole-genome sequencing data, and the need to include individuals of diverse genetic ancestries.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine,Physiology

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