Molecular Mechanisms of Vascular Health: Insights From Vascular Aging and Calcification

Author:

Sutton Nadia R.1ORCID,Malhotra Rajeev2ORCID,St. Hilaire Cynthia3ORCID,Aikawa Elena4ORCID,Blumenthal Roger S.5ORCID,Gackenbach Grace6,Goyal Parag7ORCID,Johnson Adam8ORCID,Nigwekar Sagar U.9,Shanahan Catherine M.10ORCID,Towler Dwight A.11ORCID,Wolford Brooke N.ORCID,Chen Yabing12ORCID

Affiliation:

1. Division of Cardiovascular Medicine (N.R.S.), Michigan Medicine, Ann Arbor.

2. Cardiology Division (R.M.), Massachusetts General Hospital and Harvard Medical School, Boston.

3. Division of Cardiology, Departments of Medicine and Bioengineering, Pittsburgh Heart, Lung, and Blood Vascular Medicine Institute, University of Pittsburgh, PA (C.S.H.).

4. Cardiovascular Medicine, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA (E.A.).

5. Johns Hopkins Ciccarone Center for the Prevention of Cardiovascular Disease. Baltimore, MD (R.S.B.).

6. Division of Cardiovascular Medicine (G.G.), Michigan Medicine, Ann Arbor.

7. Department of Medicine, Weill Cornell Medicine, New York (P.G.).

8. Cardiology Division (A.J.), Massachusetts General Hospital and Harvard Medical School, Boston.

9. Division of Nephrology (S.U.N.), Massachusetts General Hospital and Harvard Medical School, Boston.

10. School of Cardiovascular and Metabolic Medicine and Sciences, King’s College London, United Kingdom (C.M.S.).

11. Department of Medicine, Endocrine Division and Pak Center for Mineral Metabolism Research, UT Southwestern Medical Center, Dallas, TX (D.A.T.).

12. K.G. Jebsen Center for Genetic Epidemiology, Department of Public Health and Nursing, Norwegian University of Science and Technology, Trondheim. Department of Pathology, University of Alabama at Birmingham and Research Department, Veterans Affairs Birmingham Medical Center (Y.C.).

Abstract

Cardiovascular disease is the most common cause of death worldwide, especially beyond the age of 65 years, with the vast majority of morbidity and mortality due to myocardial infarction and stroke. Vascular pathology stems from a combination of genetic risk, environmental factors, and the biologic changes associated with aging. The pathogenesis underlying the development of vascular aging, and vascular calcification with aging, in particular, is still not fully understood. Accumulating data suggests that genetic risk, likely compounded by epigenetic modifications, environmental factors, including diabetes and chronic kidney disease, and the plasticity of vascular smooth muscle cells to acquire an osteogenic phenotype are major determinants of age-associated vascular calcification. Understanding the molecular mechanisms underlying genetic and modifiable risk factors in regulating age-associated vascular pathology may inspire strategies to promote healthy vascular aging. This article summarizes current knowledge of concepts and mechanisms of age-associated vascular disease, with an emphasis on vascular calcification.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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