Loss of Y Chromosome in Blood Is Associated With Major Cardiovascular Events During Follow-Up in Men After Carotid Endarterectomy.

Saskia Haitjema, Daniel Kofink, Jessica van Setten, Sander W van der Laan, Arjan H Schoneveld, James Eales, Maciej Tomaszewski, Saskia C A de Jager, Gerard Pasterkamp, Folkert W Asselbergs, Hester M den Ruijter
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引用次数: 58

Abstract

Background: Recent studies found an immune regulatory role for Y chromosome and a relationship between loss of Y chromosome (LOY) in blood cells and a higher risk of cancer and mortality. Given involvement of immune cells in atherosclerosis, we hypothesized that LOY is associated with the severity of atherosclerotic plaque characteristics and outcome in men undergoing carotid endarterectomy.

Methods and results: LOY was quantified in blood and plaque from raw intensity genotyping data in men within the Athero-Express biobank study. Plaques were dissected, and the culprit lesions used for histology and the measurement of inflammatory proteins. We tested LOY for association with (inflammatory) atherosclerotic plaque phenotypes and cytokines and assessed the association of LOY with secondary events during 3-year follow-up. Of 366 patients with carotid endarterectomy, 61 exhibited some degree of LOY in blood. LOY was also present in atherosclerotic plaque lesions (n=8/242, 3%). LOY in blood was negatively associated with age (β=-0.03/10 y; r2=0.07; P=1.6×10-7) but not with cardiovascular disease severity at baseline. LOY in blood was associated with a larger atheroma size (odds ratio, 2.15; 95% confidence interval, 1.06-4.76; P=0.04); however, this association was not significant after correction for multiple testing. LOY was independently associated with secondary major cardiovascular events (hazard ratio=2.28; 95% confidence interval, 1.11-4.67; P=0.02) in blood when corrected for confounders.

Conclusions: In this hypothesis-generating study, LOY in blood is independently associated with secondary major cardiovascular events in a severely atherosclerotic population. Our data could indicate that LOY affects secondary outcome via other mechanisms than inflammation in the atherosclerotic plaque.

男性颈动脉内膜切除术后随访期间血液中Y染色体缺失与主要心血管事件相关
背景:近年来的研究发现,Y染色体具有免疫调节作用,血细胞中Y染色体的缺失与癌症和死亡率的增加有关。鉴于免疫细胞参与动脉粥样硬化,我们假设LOY与接受颈动脉内膜切除术的男性动脉粥样硬化斑块特征的严重程度和结果有关。方法和结果:在Athero-Express生物银行研究中,通过原始强度基因分型数据对男性血液和斑块中的LOY进行量化。斑块被解剖,罪魁祸首病变用于组织学和炎症蛋白的测量。我们测试了LOY与(炎性)动脉粥样硬化斑块表型和细胞因子的关系,并在3年随访期间评估了LOY与继发性事件的关系。366例颈动脉内膜切除术患者中,61例出现不同程度的LOY血。动脉粥样硬化斑块病变中也存在LOY (n=8/ 242,3 %)。血LOY与年龄呈负相关(β=-0.03/10 y;r2 = 0.07;P=1.6×10-7),但与基线时心血管疾病严重程度无关。血液中的LOY与较大的动脉粥样硬化大小相关(优势比2.15;95%置信区间为1.06-4.76;P = 0.04);然而,在多重检验校正后,这种关联并不显著。LOY与继发性主要心血管事件独立相关(风险比=2.28;95%置信区间为1.11-4.67;P=0.02),校正混杂因素后。结论:在这项产生假设的研究中,在严重动脉粥样硬化人群中,血液中的LOY与继发性主要心血管事件独立相关。我们的数据可能表明,LOY通过其他机制影响次要结局,而不是动脉粥样硬化斑块中的炎症。
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来源期刊
Circulation: Cardiovascular Genetics
Circulation: Cardiovascular Genetics CARDIAC & CARDIOVASCULAR SYSTEMS-GENETICS & HEREDITY
自引率
0.00%
发文量
0
审稿时长
6-12 weeks
期刊介绍: Circulation: Genomic and Precision Medicine considers all types of original research articles, including studies conducted in human subjects, laboratory animals, in vitro, and in silico. Articles may include investigations of: clinical genetics as applied to the diagnosis and management of monogenic or oligogenic cardiovascular disorders; the molecular basis of complex cardiovascular disorders, including genome-wide association studies, exome and genome sequencing-based association studies, coding variant association studies, genetic linkage studies, epigenomics, transcriptomics, proteomics, metabolomics, and metagenomics; integration of electronic health record data or patient-generated data with any of the aforementioned approaches, including phenome-wide association studies, or with environmental or lifestyle factors; pharmacogenomics; regulation of gene expression; gene therapy and therapeutic genomic editing; systems biology approaches to the diagnosis and management of cardiovascular disorders; novel methods to perform any of the aforementioned studies; and novel applications of precision medicine. Above all, we seek studies with relevance to human cardiovascular biology and disease.
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