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艾滋病毒感染者中CHIP患病率增加。

Increased CHIP Prevalence Amongst People Living with HIV.

作者信息

Bick Alexander G, Popadin Konstantin, Thorball Christian W, Uddin Md Mesbah, Zanni Markella, Yu Bing, Cavassini Matthias, Rauch Andri, Tarr Philip, Schmid Patrick, Bernasconi Enos, Günthard Huldrych F, Libby Peter, Boerwinkle Eric, McLaren Paul J, Ballantyne Christie M, Grinspoon Steven, Natarajan Pradeep, Fellay Jacques

机构信息

Division of Genetic Medicine, Department of Medicine, Vanderbilt University School of Medicine, Nashville, TN, USA.

School of Life Sciences, École Polytechnique Fédérale de Lausanne, Lausanne, Switzerland.

出版信息

medRxiv. 2020 Nov 7:2020.11.06.20225607. doi: 10.1101/2020.11.06.20225607.

Abstract

People living with human immunodeficiency virus (PLWH) have significantly increased risk for cardiovascular disease in part due to inflammation and immune dysregulation. Clonal hematopoiesis of indeterminate potential (CHIP), the age-related acquisition and expansion of hematopoietic stem cells due to leukemogenic driver mutations, increases risk for both hematologic malignancy and coronary artery disease (CAD). Since increased inflammation is hypothesized to be both a cause and consequence of CHIP, we hypothesized that PLWH have a greater prevalence of CHIP. We searched for CHIP in multi-ethnic cases from the Swiss HIV Cohort Study (SHCS, n=600) and controls from the Atherosclerosis Risk in the Communities study (ARIC, n=8,111) from blood DNA-derived exome sequences. We observed that HIV is associated with increased CHIP prevalence, both in the whole study population and in a subset of 230 cases and 1002 matched controls selected by propensity matching to control for demographic imbalances (SHCS 7%, ARIC 3%, p=0.005). Additionally, unlike in ARIC, ASXL1 was the most commonly implicated mutated CHIP gene. We propose that CHIP may be one mechanism through which PLWH are at increased risk for CAD. Larger prospective studies should evaluate the hypothesis that CHIP contributes to the excess cardiovascular risk in PLWH.

摘要

感染人类免疫缺陷病毒(HIV)的人群患心血管疾病的风险显著增加,部分原因是炎症和免疫失调。不确定潜能的克隆性造血(CHIP)是由于致白血病驱动基因突变导致的与年龄相关的造血干细胞获得和扩增,它会增加血液系统恶性肿瘤和冠状动脉疾病(CAD)的风险。由于炎症增加被认为是CHIP的原因和结果,我们推测HIV感染者中CHIP的患病率更高。我们从瑞士HIV队列研究(SHCS,n = 600)的多民族病例以及社区动脉粥样硬化风险研究(ARIC,n = 8111)的对照中,通过血液DNA衍生的外显子组序列搜索CHIP。我们观察到,在整个研究人群中以及在通过倾向匹配选择的230例病例和1002例匹配对照的子集中(SHCS为7%,ARIC为3%,p = 0.005),HIV都与CHIP患病率增加相关。此外,与ARIC不同,ASXL1是最常涉及的CHIP突变基因。我们提出,CHIP可能是HIV感染者患CAD风险增加的一种机制。更大规模的前瞻性研究应评估CHIP导致HIV感染者心血管风险过高这一假说。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/832a/7654930/238825138341/nihpp-2020.11.06.20225607-f0001.jpg

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