Cardiovascular Disease, Aging, and Clonal Hematopoiesis
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...
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Veröffentlicht in: | Annual review of pathology 2020-01, Vol.15 (1), p.419-438 |
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description | 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. |
doi_str_mv | 10.1146/annurev-pathmechdis-012419-032544 |
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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.</description><subject>age-related clonal hematopoiesis</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Aging - genetics</subject><subject>Aging - physiology</subject><subject>ARCH</subject><subject>Cardiovascular Diseases - epidemiology</subject><subject>Cardiovascular Diseases - etiology</subject><subject>Cells, Cultured</subject><subject>CHIP</subject><subject>Clonal Evolution - physiology</subject><subject>clonal hematopoiesis of indeterminate potential</subject><subject>DNMT3A</subject><subject>Hematopoiesis - genetics</subject><subject>Hematopoiesis - physiology</subject><subject>Humans</subject><subject>IL-1β</subject><subject>Incidence</subject><subject>Mutation - physiology</subject><subject>Risk Factors</subject><subject>somatic mutations</subject><subject>TET2</subject><issn>1553-4006</issn><issn>1553-4014</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqdkU1Lw0AQhhdRbK3-BclRodH9Sja5CCVaKxS86HmZbjbtSpKNu0nFf29KaqlXmcMO7MszwzwI3RJ8RwiP76GuO6e3YQPtptJqkxsfYkI5SUPMaMT5CRqTKGIhx4SfHnocj9CF9x8YcxYnyTkaMRInKRNkjEQGLjd2C151Jbjg0XgNXk-D2drU62kAdR5kpa2hDBa6gtY21mhv_CU6K6D0-mr_TtD7_OktW4TL1-eXbLYMIRJxG4pERDiNMaiC5ZFIlMgLQXc7M6YZjYERsYKC0STSChdUAC-KOFU5AZVSyNkEPQzcpltVOle6bh2UsnGmAvctLRj596c2G7m2WykI5lGa9ICbPcDZz077VlbGK12WUGvbeUkZof2ZaF8TNBuiylnvnS4OYwiWOwFyL0AeCZCDADkI6BnXx_seCL8X7wPzIbBjQdnTjP7y_5j0A_KKodQ</recordid><startdate>20200124</startdate><enddate>20200124</enddate><creator>Evans, Megan A</creator><creator>Sano, Soichi</creator><creator>Walsh, Kenneth</creator><general>Annual Reviews</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20200124</creationdate><title>Cardiovascular Disease, Aging, and Clonal Hematopoiesis</title><author>Evans, Megan A ; Sano, Soichi ; Walsh, Kenneth</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a576t-78750960acf3d578c7df72012433e326a317baf3285ec0f27a4ff69cd1ac92ad3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>age-related clonal hematopoiesis</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Aging - genetics</topic><topic>Aging - physiology</topic><topic>ARCH</topic><topic>Cardiovascular Diseases - epidemiology</topic><topic>Cardiovascular Diseases - etiology</topic><topic>Cells, Cultured</topic><topic>CHIP</topic><topic>Clonal Evolution - physiology</topic><topic>clonal hematopoiesis of indeterminate potential</topic><topic>DNMT3A</topic><topic>Hematopoiesis - genetics</topic><topic>Hematopoiesis - physiology</topic><topic>Humans</topic><topic>IL-1β</topic><topic>Incidence</topic><topic>Mutation - physiology</topic><topic>Risk Factors</topic><topic>somatic mutations</topic><topic>TET2</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Evans, Megan A</creatorcontrib><creatorcontrib>Sano, Soichi</creatorcontrib><creatorcontrib>Walsh, Kenneth</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Annual review of pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Evans, Megan A</au><au>Sano, Soichi</au><au>Walsh, Kenneth</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cardiovascular Disease, Aging, and Clonal Hematopoiesis</atitle><jtitle>Annual review of pathology</jtitle><addtitle>Annu Rev Pathol</addtitle><date>2020-01-24</date><risdate>2020</risdate><volume>15</volume><issue>1</issue><spage>419</spage><epage>438</epage><pages>419-438</pages><issn>1553-4006</issn><eissn>1553-4014</eissn><abstract>Traditional risk factors are incompletely predictive of cardiovascular disease development, a leading cause of death in the elderly. 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subjects | age-related clonal hematopoiesis Aged Aged, 80 and over Aging - genetics Aging - physiology ARCH Cardiovascular Diseases - epidemiology Cardiovascular Diseases - etiology Cells, Cultured CHIP Clonal Evolution - physiology clonal hematopoiesis of indeterminate potential DNMT3A Hematopoiesis - genetics Hematopoiesis - physiology Humans IL-1β Incidence Mutation - physiology Risk Factors somatic mutations TET2 |
title | Cardiovascular Disease, Aging, and Clonal Hematopoiesis |
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