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首页> 外文期刊>Epigenetics: official journal of the DNA Methylation Society >Repetitive element dna methylation and circulating endothelial and inflammation markers in the VA normative aging study
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Repetitive element dna methylation and circulating endothelial and inflammation markers in the VA normative aging study

机译:VA规范性衰老研究中的重复元素dna甲基化和循环内皮和炎症标志物

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摘要

Background: Lower blood DNA methylation has been associated with atherosclerosis and high cardiovascular risk. Mechanisms linking DNA hypomethylation to increased cardiovascular risk are still largely unknown. In a population of community-dwelling elderly individuals, we evaluated whether DNA methylation in LINE-1 repeti- tive element, heavily methylated sequences dispersed throughout the human genome, was associated with circulating Vascular cell Adhesion Molecule-1 (VcAM-1), Inter-cellular Adhesion Molecule-1 (IcAM-1) and c-reactive protein (cRp). Methods and results: We measured LINE-1 methylation by bisulfite pcR-pyrosequencing on 742 blood DNA samples from male participants in the Boston area Normative Aging study (mean age = 74.8 years). Mean serum VcAM-1 in- creased progressively in association with LINE-1 hypomethylation (from 975.2 to 1063.4 ng/ml in the highest vs. lowest methylation quintiles; p trend = 0.004). The association between VcAM-1 and LINE-1 hypomethylation was significant in individuals without ischemic heart disease or stroke (n = 480; p = 0.001), but not in those with prevalent disease (n = 262; p = 0.57). serum IcAM-1 and cRp were not associated with LINE-1 methylation (p trend = >0.25). All results were con- firmed by multivariable analyses adjusting for age, BMI, smoking, pack-years and ischemic heart disease/stroke. conclusions: LINE-1 element hypomethylation is associated with higher serum VCAM-1. Our data provide new insights into epigenetic events that may accompany the development of cardiovascular disease.
机译:背景:较低的血液DNA甲基化与动脉粥样硬化和高心血管风险有关。将DNA低甲基化与心血管疾病风险增加联系起来的机制仍然未知。在一个社区居住的老年人群中,我们评估了LINE-1重复元件中的DNA甲基化(分布在整个人类基因组中的高度甲基化的序列)是否与循环中的血管细胞粘附分子1(VcAM-1),细胞粘附分子1(IcAM-1)和c反应蛋白(cRp)。方法和结果:我们在波士顿地区规范性衰老研究(平均年龄= 74.8岁)中,从742名来自男性参与者的血液DNA样品中,通过亚硫酸氢盐pcR-焦磷酸测序对LINE-1甲基化进行了测量。平均血清VcAM-1随LINE-1低甲基化而逐渐增加(最高甲基化组和最低甲基化组之间从975.2 ng / ml降至1063.4 ng / ml; p趋势= 0.004)。 VcAM-1和LINE-1低甲基化之间的关联在无缺血性心脏病或中风的个体中具有显着意义(n = 480; p = 0.001),而在那些患有流行性心脏病(n = 262; p = 0.57)的人群中则没有。血清IcAM-1和cRp与LINE-1甲基化无关(p趋势=> 0.25)。所有结果均通过针对年龄,BMI,吸烟,吸烟年数和缺血性心脏病/中风进行校正的多变量分析得到证实。结论:LINE-1元件的低甲基化与血清VCAM-1升高有关。我们的数据提供了对可能伴随心血管疾病发展的表观遗传事件的新见解。

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