Somatic Mutations and Clonal Hematopoiesis: Unexpected Potential New Drivers of Age-Related Cardiovascular Disease

被引:118
作者
Fuster, Jose J. [1 ]
Walsh, Kenneth [1 ]
机构
[1] Boston Univ, Sch Med, Whitaker Cardiovasc Inst, Mol Cardiol Unit, Boston, MA 02215 USA
基金
美国国家卫生研究院;
关键词
aging; atherosclerosis; cardiovascular disease; CHIP; inflammation; risk factors; JAK2 V617F MUTATION; INTERLEUKIN-1 INDUCES INTERLEUKIN-1; DNA METHYLTRANSFERASE 3A; CEREBRAL VENOUS THROMBOSIS; X-INACTIVATION PATTERNS; POLYCYTHEMIA-VERA; STEM-CELLS; SUBCLINICAL ATHEROSCLEROSIS; ESSENTIAL THROMBOCYTHEMIA; RISK-FACTORS;
D O I
10.1161/CIRCRESAHA.117.312115
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Increasing evidence shows that conventional cardiovascular risk factors are incompletely predictive of cardiovascular disease, particularly in elderly individuals, suggesting that there may still be unidentified causal risk factors. Although the accumulation of somatic DNA mutations is a hallmark of aging, its relevance in cardiovascular disease or other age-related conditions has been, with the exception of cancer, largely unexplored. Here, we review recent clinical and preclinical studies that have identified acquired mutations in hematopoietic stem cells and subsequent clonal hematopoiesis as a new cardiovascular risk factor and a potential major driver of atherosclerosis. Understanding the mechanisms underlying the connection between somatic mutation-driven clonal hematopoiesis and cardiovascular disease will be highly relevant in the context of personalized medicine, as it may provide key information for the design of diagnostic, preventive, or therapeutic strategies tailored to the effects of specific somatic mutations.
引用
收藏
页码:523 / 532
页数:10
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