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基于孟德尔随机化的中度饮酒与心血管疾病。

Moderate alcohol use and cardiovascular disease from Mendelian randomization.

机构信息

Lifestyle and Lifecourse Epidemiology Group, School of Public Health, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China.

出版信息

PLoS One. 2013 Jul 16;8(7):e68054. doi: 10.1371/journal.pone.0068054. Print 2013.

Abstract

BACKGROUND

Observational studies show moderate alcohol use negatively associated with ischemic heart disease (IHD) and cardiovascular disease (CVD). However, healthier attributes among moderate users compared to never users may confound the apparent association. A potentially less biased way to examine the association is Mendelian randomization, using alcohol metabolizing genes which influence alcohol use.

METHODS

We used instrumental variable analysis with aldehyde dehydrogenase 2 (ALDH2) genotypes (AA/GA/GG) as instrumental variables for alcohol use to examine the association of alcohol use (10 g ethanol/day) with CVD risk factors (blood pressure, lipids and glucose) and morbidity (self-reported IHD and CVD) among men in the Guangzhou Biobank Cohort Study.

RESULTS

ALDH2 genotypes were a credible instrument for alcohol use (F-statistic 74.6). Alcohol was positively associated with HDL-cholesterol (0.05 mmol/L per alcohol unit, 95% confidence interval (CI) 0.02 to 0.08) and diastolic blood pressure (1.15 mmHg, 95% CI 0.23 to 2.07) but not with systolic blood pressure (1.00 mmHg, 95% CI -0.74 to 2.74), LDL-cholesterol (0.03 mmol/L, 95% CI -0.03 to 0.08), log transformed triglycerides (0.03 mmol/L, 95% CI -0.01 to 0.08) or log transformed fasting glucose (0.01 mmol/L, 95% CI -0.006 to 0.03), self-reported CVD (odds ratio (OR) 0.98, 95% CI 0.76 to 1.27) or self-reported IHD (OR 1.10, 95% CI 0.83 to 1.45).

CONCLUSION

Low to moderate alcohol use among men had the expected effects on most CVD risk factors but not fasting glucose. Larger studies are needed to confirm the null associations with IHD, CVD and fasting glucose.

摘要

背景

观察性研究表明,适量饮酒与缺血性心脏病(IHD)和心血管疾病(CVD)呈负相关。然而,与从不饮酒者相比,适度饮酒者的健康属性可能会混淆这种明显的关联。一种潜在的偏差较小的方法是孟德尔随机化,使用影响饮酒的酒精代谢基因作为工具变量。

方法

我们使用乙醛脱氢酶 2(ALDH2)基因型(AA/GA/GG)作为饮酒的工具变量进行工具变量分析,以检查饮酒(每天 10 克乙醇)与 CVD 危险因素(血压、血脂和血糖)以及广州生物库队列研究中男性的发病率(自述 IHD 和 CVD)之间的关联。

结果

ALDH2 基因型是饮酒的可信工具(F 统计量为 74.6)。饮酒与高密度脂蛋白胆固醇呈正相关(每单位酒精增加 0.05mmol/L,95%置信区间(CI)为 0.02 至 0.08)和舒张压(1.15mmHg,95%CI 为 0.23 至 2.07),但与收缩压(1.00mmHg,95%CI 为 -0.74 至 2.74)、LDL 胆固醇(0.03mmol/L,95%CI 为 -0.03 至 0.08)、对数转换甘油三酯(0.03mmol/L,95%CI 为 -0.01 至 0.08)或空腹血糖(0.01mmol/L,95%CI 为 -0.006 至 0.03)、自述 CVD(比值比(OR)为 0.98,95%CI 为 0.76 至 1.27)或自述 IHD(OR 为 1.10,95%CI 为 0.83 至 1.45)无关。

结论

男性低至中度饮酒对大多数 CVD 危险因素有预期的影响,但对空腹血糖没有影响。需要更大的研究来证实与 IHD、CVD 和空腹血糖的零关联。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb2b/3712994/798a76862a62/pone.0068054.g001.jpg

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