Division of Human Nutrition and Health, Wageningen University, Wageningen, The Netherlands.
Am J Clin Nutr. 2022 Mar 4;115(3):633-642. doi: 10.1093/ajcn/nqab366.
Population-based studies generally show J-shaped associations between alcohol intake and mortality from cardiovascular disease (CVD). Little is known about alcohol and long-term mortality risk after myocardial infarction (MI).
We examined alcohol intake in relation to all-cause, CVD, and ischemic heart disease (IHD) mortality in Dutch post-MI patients of the Alpha Omega Cohort.
The analysis comprised 4365 patients (60-80 years; 79% male) with an MI ≤ 10 years before study enrolment. We used a 203-item FFQ to assess alcohol (total ethanol) and dietary intakes over the past month. Patients were classified as nondrinkers (0 g/d; n = 956) or very light (>0 to 2 g/d; n = 385), light (M: >2 to 10 g/d; F: >2 to 5 g/d; n = 1125), moderate (M: >10 to 30 g/d; F: >5 to 15 g/d; n = 1207), or heavy drinkers (M: >30 g/d; F: >15 g/d; n = 692). HRs of mortality for alcohol intake were obtained from Cox models, adjusting for age, sex, education, smoking, BMI, physical activity, and dietary factors.
Alcohol was consumed by 83% of males and 61% of females. During ∼12 years of follow-up, 2035 deaths occurred, of which 903 were from CVD and 558 were from IHD. Compared to the (combined) reference group of nondrinkers and very light drinkers, HRs for all-cause mortality were 0.87 (95% CI, 0.78-0.98), 0.85 (95% CI, 0.75-0.96), and 0.91 (95% CI, 0.79-1.04) for light, moderate, and heavy drinkers, respectively. For CVD mortality, corresponding HRs were 0.80 (95% CI, 0.67-0.96), 0.82 (95% CI, 0.69-0.98), and 0.87 (95% CI, 0.70-1.08) for light, moderate, and heavy drinkers, respectively. Findings for IHD mortality were similar. HRs did not materially change when nondrinkers or very light drinkers were taken as the reference, or after exclusion of former drinkers or patients with diabetes or poor/moderate self-rated health.
Light and moderate alcohol intakes were inversely associated with mortality risk in stable post-MI patients. These observational findings should be cautiously interpreted in light of the total evidence on alcohol and health. The Alpha Omega Cohort is registered at clinicaltrials.gov as NCT03192410.
基于人群的研究普遍表明,酒精摄入量与心血管疾病(CVD)死亡率之间呈 J 型关联。关于心肌梗死后(MI)患者的酒精摄入量与长期死亡率之间的关系知之甚少。
我们研究了荷兰 MI 后 Alpha Omega 队列中患者的酒精摄入量与全因、CVD 和缺血性心脏病(IHD)死亡率之间的关系。
该分析包括 4365 名年龄在 60-80 岁(79%为男性)、MI 发生在研究入组前 10 年以内的患者。我们使用 203 项食物频率问卷(FFQ)来评估过去一个月内的酒精(总乙醇)和饮食摄入量。患者被分为不饮酒者(0 g/d;n=956)或极少量饮酒者(>0 至 2 g/d;n=385)、少量饮酒者(男性:>2 至 10 g/d;女性:>2 至 5 g/d;n=1125)、适量饮酒者(男性:>10 至 30 g/d;女性:>5 至 15 g/d;n=1207)或大量饮酒者(男性:>30 g/d;女性:>15 g/d;n=692)。使用 Cox 模型获得死亡率的 HR,该模型调整了年龄、性别、教育程度、吸烟、BMI、体力活动和饮食因素。
83%的男性和 61%的女性饮酒。在大约 12 年的随访期间,发生了 2035 例死亡,其中 903 例死于 CVD,558 例死于 IHD。与(合并)不饮酒和极少量饮酒者的参考组相比,全因死亡率的 HR 分别为 0.87(95%CI,0.78-0.98)、0.85(95%CI,0.75-0.96)和 0.91(95%CI,0.79-1.04),分别为轻、中、重度饮酒者。对于 CVD 死亡率,相应的 HR 分别为 0.80(95%CI,0.67-0.96)、0.82(95%CI,0.69-0.98)和 0.87(95%CI,0.70-1.08),分别为轻、中、重度饮酒者。IHD 死亡率的结果相似。当将不饮酒者或极少量饮酒者作为参考时,或在排除前饮酒者或患有糖尿病或自我报告健康状况较差/中等的患者后,HR 没有实质性变化。
稳定的 MI 后患者中,轻度和中度饮酒与死亡率风险呈负相关。鉴于关于酒精和健康的总体证据,应谨慎解释这些观察性发现。Alpha Omega 队列在 clinicaltrials.gov 上注册为 NCT03192410。