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克隆性造血:血细胞中的体细胞突变与动脉粥样硬化。

Clonal Hematopoiesis: Somatic Mutations in Blood Cells and Atherosclerosis.

机构信息

Center for Genomic Medicine and Cardiovascular Research Center, Massachusetts General Hospital, Boston (P.N., S.K.).

Program in Medical and Population Genetics and Cardiovascular Disease Initiative, Broad Institute of Harvard and MIT, Cambridge, MA (P.N., S.K.).

出版信息

Circ Genom Precis Med. 2018 Jul;11(7):e001926. doi: 10.1161/CIRCGEN.118.001926.

DOI:10.1161/CIRCGEN.118.001926
PMID:29987111
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6082163/
Abstract

The most important prognostic factor for atherosclerotic cardiovascular disease is age, independent of all other recognized risk factors. Recently, exome sequence analyses showed that somatic mutations in blood cells, a process termed clonal hematopoiesis, are common and increase in prevalence with age, with at least 1 in 10 adults older than 70 years affected. Carriers of clonal hematopoiesis have been shown to be not only at heightened risk for hematologic malignancy but also at increased risk for atherosclerotic cardiovascular disease. Here, we review the prior literature of clonal selection and expansion of hematopoietic stem cells and the evidence supporting its causal association with atherosclerotic cardiovascular disease.

摘要

动脉粥样硬化性心血管疾病最重要的预后因素是年龄,独立于所有其他公认的危险因素。最近,外显子组序列分析表明,血细胞中的体细胞突变,即所谓的克隆性造血,很常见,且随着年龄的增长而增加,至少有 1/10 的 70 岁以上成年人受到影响。已经证明,克隆性造血的携带者不仅患血液恶性肿瘤的风险增加,而且患动脉粥样硬化性心血管疾病的风险也增加。在这里,我们回顾了造血干细胞克隆选择和扩增的既往文献,并提供了支持其与动脉粥样硬化性心血管疾病因果关系的证据。

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本文引用的文献

1
Hematopoietic lineage distribution and evolutionary dynamics of clonal hematopoiesis.克隆性造血的造血谱系分布和进化动态。
Leukemia. 2018 Sep;32(9):1908-1919. doi: 10.1038/s41375-018-0047-7. Epub 2018 Mar 1.
2
Somatic Mutations and Clonal Hematopoiesis: Unexpected Potential New Drivers of Age-Related Cardiovascular Disease.体细胞突变和克隆性造血:年龄相关性心血管疾病的潜在新驱动因素。
Circ Res. 2018 Feb 2;122(3):523-532. doi: 10.1161/CIRCRESAHA.117.312115.
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Clonal Hematopoiesis and Evolution to Hematopoietic Malignancies.克隆性造血与向造血系统恶性肿瘤的演变。
Cell Stem Cell. 2018 Feb 1;22(2):157-170. doi: 10.1016/j.stem.2018.01.011.
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Relationship of C-reactive protein reduction to cardiovascular event reduction following treatment with canakinumab: a secondary analysis from the CANTOS randomised controlled trial.卡那单抗治疗后 C 反应蛋白降低与心血管事件减少的关系:来自 CANTOS 随机对照试验的二次分析。
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Exome-wide association study of plasma lipids in >300,000 individuals.对超过30万人的血浆脂质进行全外显子组关联研究。
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MECOM, HBS1L-MYB, THRB-RARB, JAK2, and TERT polymorphisms defining the genetic predisposition to myeloproliferative neoplasms: A study on 939 patients.MECOM、HBS1L-MYB、THRB-RARB、JAK2 和 TERT 多态性定义了骨髓增生性肿瘤的遗传易感性:对 939 例患者的研究。
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Lancet. 2017 Sep 16;390(10100):1151-1210. doi: 10.1016/S0140-6736(17)32152-9.
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Effect of interleukin-1β inhibition with canakinumab on incident lung cancer in patients with atherosclerosis: exploratory results from a randomised, double-blind, placebo-controlled trial.卡那单抗抑制白细胞介素-1β对动脉粥样硬化患者肺癌发病的影响:一项随机、双盲、安慰剂对照试验的探索性结果。
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Antiinflammatory Therapy with Canakinumab for Atherosclerotic Disease.卡那奴单抗治疗动脉粥样硬化疾病的抗炎疗法。
N Engl J Med. 2017 Sep 21;377(12):1119-1131. doi: 10.1056/NEJMoa1707914. Epub 2017 Aug 27.
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