Wei Li, Liu Shuchuan, Su Zhendong, Cheng Rongchao, Bai Xiuping, Li Xueqi
Department of Cardiology, The Fourth Affiliated Hospital, Harbin Medical University, Harbin, China.
Department of Hematology, The First Affiliated Hospital, Harbin Medical University, Harbin, China.
Arq Bras Cardiol. 2014 May;102(5):481-8. doi: 10.5935/abc.20140054. Epub 2014 May 9.
Global methylation level in blood leukocyte DNA has been associated with the risk of coronary heart disease (CHD), with inconsistent results in various populations. Similar data are lacking in Chinese population where different genetic, lifestyle and environmental factors may affect DNA methylation and its risk relationship with CHD.
To examine whether global methylation is associated with the risk of CHD in Chinese population.
A total of 334 cases with CHD and 788 healthy controls were included. Global methylation in blood leukocyte DNA was estimated by analyzing LINE-1 repeats using bisulfite pyrosequencing.
In an initial analysis restricted to control subjects, LINE-1 level reduced significantly with aging, elevated total cholesterol, and diagnosis of diabetes. In the case-control analysis, reduced LINE-1 methylation was associated with increased risk of CHD; analysis by quartile revealed odds ratios (95%CI) of 0.9 (0.6-1.4), 1.9 (1.3-2.9) and 2.3 (1.6-3.5) for the third, second and first (lowest) quartile (Ptrend < 0.001), respectively, compared to the fourth (highest) quartile. Lower (<median) LINE-1 methylation was associated with a 2.2-fold (95%CI = 1.7-3.0) increased risk of CHD. The lower LINE-1-related CHD risk estimates tended to be stronger among subjects with the highest tertile of homocysteine (Pinteraction = 0.042) and those with diagnosis of hypertension (Pinteraction = 0.012).
LINE-1 hypomethylation is associated with the risk of CHD in Chinese population. Potential CHD risk factors such as older age, elevated total cholesterol, and diagnosis of diabetes may have impact on global DNA methylation, whereby exerting their effect on CHD risk.
血液白细胞DNA的整体甲基化水平与冠心病(CHD)风险相关,但在不同人群中的结果并不一致。中国人群中缺乏类似数据,因为不同的遗传、生活方式和环境因素可能会影响DNA甲基化及其与冠心病的风险关系。
研究整体甲基化是否与中国人群的冠心病风险相关。
共纳入334例冠心病患者和788例健康对照。通过亚硫酸氢盐焦磷酸测序分析LINE-1重复序列,估计血液白细胞DNA的整体甲基化水平。
在最初仅限于对照受试者的分析中,LINE-1水平随着年龄增长、总胆固醇升高和糖尿病诊断而显著降低。在病例对照分析中,LINE-1甲基化降低与冠心病风险增加相关;按四分位数分析显示,与第四(最高)四分位数相比,第三、第二和第一(最低)四分位数的比值比(95%CI)分别为0.9(0.6-1.4)、1.9(1.3-2.9)和2.3(1.6-3.5)(Ptrend<0.001)。较低(<中位数)的LINE-1甲基化与冠心病风险增加2.2倍(95%CI=1.7-3.0)相关。在同型半胱氨酸最高三分位数的受试者(P交互作用=0.042)和诊断为高血压的受试者(P交互作用=0.012)中,较低的与LINE-1相关的冠心病风险估计往往更强。
LINE-1低甲基化与中国人群的冠心病风险相关。年龄较大、总胆固醇升高和糖尿病诊断等潜在的冠心病风险因素可能会影响整体DNA甲基化,从而对冠心病风险产生影响。