Cardiovascular Disease, Aging, and Clonal Hematopoiesis.

IF 28.4 1区 医学 Q1 PATHOLOGY
M. A. Evans, S. Sano, K. Walsh
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引用次数: 83

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. Expected final online publication date for the Annual Review of Pathology: Mechanisms of Disease, Volume 15 is January 24, 2020. Please see http://www.annualreviews.org/page/journal/pubdates for revised estimates.
心血管疾病、衰老和克隆造血。
传统的危险因素不能完全预测心血管疾病的发展,这是老年人死亡的主要原因。最近的流行病学研究表明,人类衰老与造血系统中体细胞突变的频率增加有关,这为突变细胞提供了竞争优势,从而允许其克隆扩增,这种现象称为克隆造血。出乎意料的是,这些突变与心血管疾病的高发病率有关,这表明造血细胞体细胞突变与心血管疾病之间存在以前未被认识到的联系。在这里,我们提供克隆造血及其与衰老和心血管疾病的关系的最新综述。我们还提供了一份详细的实验研究报告,这些研究有助于理解克隆造血与心血管疾病之间的关系,并阐明了造血体细胞突变导致疾病病理的机制。《病理学年度评论:疾病机制》第15卷预计最终在线出版日期为2020年1月24日。修订后的估计数请参阅http://www.annualreviews.org/page/journal/pubdates。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
62.60
自引率
0.00%
发文量
40
期刊介绍: The Annual Review of Pathology: Mechanisms of Disease is a scholarly journal that has been published since 2006. Its primary focus is to provide a comprehensive overview of recent advancements in our knowledge of the causes and development of significant human diseases. The journal places particular emphasis on exploring the current and evolving concepts of disease pathogenesis, as well as the molecular genetic and morphological changes associated with various diseases. Additionally, the journal addresses the clinical significance of these findings. In order to increase accessibility and promote the broad dissemination of research, the current volume of the journal has transitioned from a gated subscription model to an open access format. This change has been made possible through the Annual Reviews' Subscribe to Open program, which allows all articles published in this volume to be freely accessible to readers. As part of this transition, all articles in the journal are published under a Creative Commons Attribution (CC BY) license, which encourages open sharing and use of the research.
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