Christensen Anne I, Nordestgaard Børge G, Tolstrup Janne S
National Institute of Public Health, University of Southern Denmark, Copenhagen, Denmark.
Department of Clinical Biochemistry, Herlev and Gentofte Hospital, Copenhagen University Hospital, Herlev, Denmark.
J Stroke. 2018 May;20(2):218-227. doi: 10.5853/jos.2017.01466. Epub 2018 May 31.
To test whether alcohol intake, both observational and estimated by genetic instruments, is associated with risk of ischemic and haemorrhagic stroke.
We used data from the Copenhagen City Heart Study 1991 to 1994 and 2001 to 2003, and the Copenhagen General Population Study 2003 to 2012 (n=78,546). As measure of alcohol exposure, self-reported consumption and genetic variation in alcohol metabolizing genes (alcohol dehydrogenase and ) as instrumental variables were used. Stroke diagnoses were obtained from a validated hospital register.
During follow-up 2,535 cases of ischemic and haemorrhagic stroke occurred. Low and moderate alcohol intake (1 to 20 drinks/week) was associated with reduced risk of stroke. The hazard ratios associated with drinking 1 to 6, 7 to 13, and 14 to 20 drinks/week were 0.84 (95% confidence interval [CI], 0.76 to 0.92), 0.83 (95% CI, 0.73 to 0.94), and 0.84 (95% CI, 0.73 to 0.97), respectively, compared with drinking <1 drink/day. and genotypes were not associated with risk of stroke. Further analysis to test the included measures revealed that increasing alcohol intake (per 1 drink/day) was positively associated with risk of alcoholic liver cirrhosis, but not associated with risk of stroke, and that increasing blood pressure (per systolic 10 mm Hg) was not associated with risk of alcoholic liver cirrhosis, but positively associated with risk of stroke.
Low and moderate self-reported alcohol intake was associated with reduced risk of stroke. The result was not supported by the result from the causal genetic analysis.
通过观察性研究以及基因手段估计饮酒量,来检验其与缺血性和出血性中风风险之间的关联。
我们使用了哥本哈根城市心脏研究1991年至1994年以及2001年至2003年的数据,还有哥本哈根普通人群研究2003年至2012年的数据(n = 78,546)。作为酒精暴露的衡量指标,使用了自我报告的饮酒量以及酒精代谢基因(乙醇脱氢酶和)的基因变异作为工具变量。中风诊断来自经过验证的医院登记册。
在随访期间,共发生了2535例缺血性和出血性中风病例。低至中度饮酒量(每周1至20杯)与中风风险降低相关。与每天饮酒量<1杯相比,每周饮酒1至6杯、7至13杯以及14至20杯的风险比分别为0.84(95%置信区间[CI],0.76至0.92)、0.83(95%CI,0.73至0.94)以及0.84(95%CI,0.73至0.97)。[具体基因名称]基因型与中风风险无关。进一步分析所纳入的指标发现,饮酒量增加(每增加1杯/天)与酒精性肝硬化风险呈正相关,但与中风风险无关;而血压升高(收缩压每升高10 mmHg)与酒精性肝硬化风险无关,但与中风风险呈正相关。
自我报告的低至中度饮酒量与中风风险降低相关。因果基因分析结果不支持这一结果。