Clinical Trial Service Unit and Epidemiological Studies Unit, Nuffield Department of Population Health, University of Oxford, Oxford, England.
Medical Research Council Population Health Research Unit, Nuffield Department of Population Health, University of Oxford, Oxford, England.
JAMA Cardiol. 2018 Mar 1;3(3):225-234. doi: 10.1001/jamacardio.2017.5205.
Current guidelines advocate the use of marine-derived omega-3 fatty acids supplements for the prevention of coronary heart disease and major vascular events in people with prior coronary heart disease, but large trials of omega-3 fatty acids have produced conflicting results.
To conduct a meta-analysis of all large trials assessing the associations of omega-3 fatty acid supplements with the risk of fatal and nonfatal coronary heart disease and major vascular events in the full study population and prespecified subgroups.
This meta-analysis included randomized trials that involved at least 500 participants and a treatment duration of at least 1 year and that assessed associations of omega-3 fatty acids with the risk of vascular events.
Aggregated study-level data were obtained from 10 large randomized clinical trials. Rate ratios for each trial were synthesized using observed minus expected statistics and variances. Summary rate ratios were estimated by a fixed-effects meta-analysis using 95% confidence intervals for major diseases and 99% confidence intervals for all subgroups.
The main outcomes included fatal coronary heart disease, nonfatal myocardial infarction, stroke, major vascular events, and all-cause mortality, as well as major vascular events in study population subgroups.
Of the 77 917 high-risk individuals participating in the 10 trials, 47 803 (61.4%) were men, and the mean age at entry was 64.0 years; the trials lasted a mean of 4.4 years. The associations of treatment with outcomes were assessed on 6273 coronary heart disease events (2695 coronary heart disease deaths and 2276 nonfatal myocardial infarctions) and 12 001 major vascular events. Randomization to omega-3 fatty acid supplementation (eicosapentaenoic acid dose range, 226-1800 mg/d) had no significant associations with coronary heart disease death (rate ratio [RR], 0.93; 99% CI, 0.83-1.03; P = .05), nonfatal myocardial infarction (RR, 0.97; 99% CI, 0.87-1.08; P = .43) or any coronary heart disease events (RR, 0.96; 95% CI, 0.90-1.01; P = .12). Neither did randomization to omega-3 fatty acid supplementation have any significant associations with major vascular events (RR, 0.97; 95% CI, 0.93-1.01; P = .10), overall or in any subgroups, including subgroups composed of persons with prior coronary heart disease, diabetes, lipid levels greater than a given cutoff level, or statin use.
This meta-analysis demonstrated that omega-3 fatty acids had no significant association with fatal or nonfatal coronary heart disease or any major vascular events. It provides no support for current recommendations for the use of such supplements in people with a history of coronary heart disease.
目前的指南主张使用源自海洋的 omega-3 脂肪酸补充剂来预防有先前冠心病的人发生冠心病和主要血管事件,但大型 omega-3 脂肪酸试验的结果相互矛盾。
对所有大型试验进行荟萃分析,评估 omega-3 脂肪酸补充剂与全人群和预先指定亚组中致命和非致命冠心病及主要血管事件风险的相关性。
本荟萃分析包括至少有 500 名参与者且治疗时间至少 1 年的随机试验,评估了 omega-3 脂肪酸与血管事件风险的相关性。
从 10 项大型随机临床试验中获得汇总的研究水平数据。使用观察到的减去预期统计量和方差对每个试验的比率进行综合。使用主要疾病的 95%置信区间和所有亚组的 99%置信区间,通过固定效应荟萃分析估计汇总比率比。
主要结局包括致命性冠心病、非致死性心肌梗死、中风、主要血管事件和全因死亡率,以及研究人群亚组中的主要血管事件。
在参与 10 项试验的 77917 名高危个体中,47803 名(61.4%)为男性,入组时的平均年龄为 64.0 岁;试验平均持续时间为 4.4 年。在 6273 例冠心病事件(2695 例冠心病死亡和 2276 例非致死性心肌梗死)和 12001 例主要血管事件上评估了治疗与结局的相关性。随机分配接受 omega-3 脂肪酸补充剂(二十碳五烯酸剂量范围,226-1800mg/d)与冠心病死亡(比率比[RR],0.93;99%置信区间[CI],0.83-1.03;P=0.05)、非致死性心肌梗死(RR,0.97;99%CI,0.87-1.08;P=0.43)或任何冠心病事件(RR,0.96;95%CI,0.90-1.01;P=0.12)均无显著相关性。随机分配接受 omega-3 脂肪酸补充剂与主要血管事件(RR,0.97;95%CI,0.93-1.01;P=0.10)、总体或任何亚组(包括有先前冠心病、糖尿病、血脂水平高于特定截定点或使用他汀类药物的亚组)均无显著相关性。
本荟萃分析表明,omega-3 脂肪酸与致命或非致命性冠心病或任何主要血管事件均无显著相关性。这不能支持目前建议有冠心病史的人使用此类补充剂的建议。