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在一项中国人群的同胞研究中,ABCG1 和 APOE 基因甲基化与缺血性卒中或其他动脉粥样硬化相关特征的总体及性别特异性关联。

Overall and sex-specific associations between methylation of the ABCG1 and APOE genes and ischemic stroke or other atherosclerosis-related traits in a sibling study of Chinese population.

机构信息

Department of Epidemiology and Biostatistics, School of Public Health, Peking University, Beijing, 100191, China.

Department of Endocrinology, The PLA Rocket Force Characteristic Medical Center, Beijing, 100085, China.

出版信息

Clin Epigenetics. 2019 Dec 10;11(1):189. doi: 10.1186/s13148-019-0784-0.

Abstract

BACKGROUND

Identifying subjects with a high risk of ischemic stroke is fundamental for prevention of the disease. Both genetic and environmental risk factors contribute to ischemic stroke, but the underlying epigenetic mechanisms which mediate genetic and environmental risk effects are not fully understood. The aim of this study was to explore whether DNA methylation loci located in the ATP-binding cassette G1 (ABCG1) and apolipoprotein E (APOE) genes, both involved in the metabolism of lipids in the body, are related to ischemic stroke, using the Fangshan/Family-based Ischemic Stroke Study in China. We also tested if these CpG sites were associated with early signs of cardiovascular atherosclerosis (carotid intima-media thickness (cIMT), ankle-brachial index (ABI), and brachial-ankle pulse wave velocity (baPWV)).

RESULTS

DNA methylation at the cg02494239 locus in ABCG1 was correlated with ischemic stroke after adjusting for gender, previous history of diabetes and hypertension, smoking, drinking, body mass index, and blood lipid levels (above vs below mean, OR = 2.416, 95% CI 1.024-5.700, P = 0.044; 75-100% percentile vs 0-25% percentile, OR = 4.461, 95% CI 1.226-16.225, P = 0.023). No statistically significant associations were observed for the cg06500161 site in ABCG1 and the cg14123992 site in APOE with ischemic stroke. The study detected that hypermethylation of the ABCG1 gene was significantly associated with cIMT, hypermethylation of the APOE gene was significantly related to ABI, and methylation of the APOE gene was statistically negatively correlated with baPWV. The above relationships demonstrated gender differences.

CONCLUSIONS

These findings suggest that epigenetic modification of ABCG1 and APOE may play a role in the pathway from disturbed blood lipid levels to the development of cardiovascular diseases. Future prospective validation of these findings is warranted.

摘要

背景

识别发生缺血性脑卒中风险较高的个体对于该疾病的预防至关重要。遗传和环境风险因素均可导致缺血性脑卒中,但介导遗传和环境风险效应的潜在表观遗传机制尚不完全清楚。本研究旨在通过中国房山/家系缺血性脑卒中研究探讨位于 ATP 结合盒转运蛋白 G1(ABCG1)和载脂蛋白 E(APOE)基因中的 DNA 甲基化位点是否与缺血性脑卒中相关,这两个基因均参与体内脂质代谢。我们还检验了这些 CpG 位点是否与心血管动脉粥样硬化的早期迹象(颈动脉内膜中层厚度(cIMT)、踝臂指数(ABI)和肱踝脉搏波速度(baPWV))相关。

结果

在调整性别、既往糖尿病和高血压病史、吸烟、饮酒、体重指数和血脂水平(高于或低于平均值)后,ABCG1 基因中的 cg02494239 位点的 DNA 甲基化与缺血性脑卒中相关(高于 vs 低于平均值,OR=2.416,95%CI1.024-5.700,P=0.044;75-100%分位 vs 0-25%分位,OR=4.461,95%CI1.226-16.225,P=0.023)。ABCG1 基因中的 cg06500161 位点和 APOE 基因中的 cg14123992 位点与缺血性脑卒中之间未观察到具有统计学意义的关联。本研究发现,ABCG1 基因的过度甲基化与 cIMT 显著相关,APOE 基因的过度甲基化与 ABI 显著相关,APOE 基因的甲基化与 baPWV 呈统计学负相关。上述关系表现出性别差异。

结论

这些发现表明,ABCG1 和 APOE 的表观遗传修饰可能在血脂紊乱导致心血管疾病发展的途径中发挥作用。有必要对这些发现进行前瞻性验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/640b/6902418/3f13af17b636/13148_2019_784_Fig1_HTML.jpg

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