DNA Methylation and High-Density Lipoprotein Functionality-Brief Report: The REGICOR Study (Registre Gironi del Cor).

S. Sayols-Baixeras, Á. Hernáez, I. Subirana, C. Lluís-Ganella, D. Muñoz, M. Fitó, J. Marrugat, R. Elosúa
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引用次数: 12

Abstract

OBJECTIVE The function of high-density lipoproteins (HDLs) may better reflect their atheroprotective role, compared with HDL-cholesterol levels. The association between DNA methylation and HDL function has not yet been established. APPROACH AND RESULTS We designed an epigenome-wide association study including 645 individuals from the REGICOR study (Registre Gironi del Cor). We determined DNA methylation from peripheral blood cells using the HumanMethylation450 array. We analyzed HDL functionality by determining HDL cholesterol efflux capacity and HDL inflammatory index. We discovered 3 methylation sites located in HOXA3, PEX5, and PER3 related to cholesterol efflux capacity and 1 located in GABRR1 related to HDL inflammatory index. Using a candidate gene approach, we also found 2 methylation sites located in CMIP related to cholesterol efflux capacity. CONCLUSIONS We identified 6 potential loci associated with HDL functionality in HOXA3, PEX5, PER3, CMIP, and GABRR1. Additional studies are warranted to validate these findings in other populations.
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DNA甲基化和高密度脂蛋白功能-简要报告:REGICOR研究(注册Gironi del Cor)。
目的与高密度脂蛋白(hdl -胆固醇)相比,高密度脂蛋白(hdl -胆固醇)的功能可能更好地反映其动脉粥样硬化的保护作用。DNA甲基化与HDL功能之间的关系尚未确定。方法和结果我们设计了一项全表观基因组关联研究,包括来自REGICOR研究的645名个体。我们使用HumanMethylation450阵列检测外周血细胞的DNA甲基化。我们通过测定HDL胆固醇外排能力和HDL炎症指数来分析HDL的功能。我们在HOXA3、PEX5和PER3中发现了3个与胆固醇外排能力相关的甲基化位点,在GABRR1中发现了1个与HDL炎症指数相关的甲基化位点。使用候选基因方法,我们还发现了位于CMIP中与胆固醇外排能力相关的2个甲基化位点。结论:我们在HOXA3、PEX5、PER3、CMIP和GABRR1中发现了6个与HDL功能相关的潜在位点。需要进一步的研究在其他人群中验证这些发现。
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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Editors and Editorial Board. Correction to: Role of LpL (Lipoprotein Lipase) in Macrophage Polarization In Vitro and In Vivo. Tribute to Paul M. Vanhoutte, MD, PhD (1940-2019). Correction to: 18F-Sodium Fluoride Imaging of Coronary Atherosclerosis in Ambulatory Patients With Diabetes Mellitus. Extracellular MicroRNA-92a Mediates Endothelial Cell-Macrophage Communication.
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