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      Cardiovascular Disease, Aging, and Clonal Hematopoiesis

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          Abstract

          Traditional risk factors are incompletely predictive of cardiovascular disease development, a leading cause of death in the elderly. Recent epidemiological studies have shown that human aging is associated with an increased frequency of somatic mutations in the hematopoietic system, which provide a competitive advantage to a mutant cell, thus allowing for its clonal expansion, a phenomenon known as clonal hematopoiesis. Unexpectedly, these mutations have been associated with a higher incidence of cardiovascular disease, suggesting a previously unrecognized connection between somatic mutations in hematopoietic cells and cardiovascular disease. Here, we provide an up-to-date review of clonal hematopoiesis and its association with aging and cardiovascular disease. We also give a detailed report of the experimental studies that have been instrumental in understanding the relationship between clonal hematopoiesis and cardiovascular disease and have shed light on the mechanisms by which hematopoietic somatic mutations contribute to disease pathology.

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          Author and article information

          Journal
          101275111
          33888
          Annu Rev Pathol
          Annu Rev Pathol
          Annual review of pathology
          1553-4006
          1553-4014
          28 February 2020
          05 November 2019
          24 January 2020
          30 March 2020
          : 15
          : 419-438
          Affiliations
          Hematovascular Biology Center and the Robert M. Berne Cardiovascular Research Center, University of Virginia School of Medicine, Charlottesville, Virginia 22908, USA;
          Author notes
          Article
          PMC7104598 PMC7104598 7104598 nihpa1567015
          10.1146/annurev-pathmechdis-012419-032544
          7104598
          31689371
          a57b69dd-b399-406d-b11a-8d187593e702
          History
          Categories
          Article

          CHIP,age-related clonal hematopoiesis,ARCH,TET2,clonal hematopoiesis of indeterminate potential,DNMT3A,IL-1β,Somatic mutations

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