Department of Medicine, University of Alberta, Edmonton, Alta.
CMAJ. 2011 Nov 8;183(16):E1189-202. doi: 10.1503/cmaj.101280. Epub 2011 Oct 11.
Statins were initially used to improve cardiovascular outcomes in people with established coronary artery disease, but recently their use has become more common in people at low cardiovascular risk. We did a systematic review of randomized trials to assess the efficacy and harms of statins in these individuals.
We searched MEDLINE and EMBASE (to Jan. 28, 2011), registries of health technology assessments and clinical trials, and reference lists of relevant reviews. We included trials that randomly assigned participants at low cardiovascular risk to receive a statin versus a placebo or no statin. We defined low risk as an observed 10-year risk of less than 20% for cardiovascular-related death or nonfatal myocardial infarction, but we explored other definitions in sensitivity analyses.
We identified 29 eligible trials involving a total of 80,711 participants. All-cause mortality was significantly lower among patients receiving a statin than among controls (relative risk [RR] 0.90, 95% confidence interval [CI] 0.84-0.97) for trials with a 10-year risk of cardiovascular disease < 20% [primary analysis] and 0.83, 95% CI 0.73-0.94, for trials with 10-year risk < 10% [sensitivity analysis]). Patients in the statin group were also significantly less likely than controls to have nonfatal myocardial infarction (RR 0.64, 95% CI 0.49-0.84) and nonfatal stroke (RR 0.81, 95% CI 0.68-0.96). Neither metaregression nor stratified analyses suggested statistically significant differences in efficacy between high-and low-potency statins, or larger reductions in cholesterol.
Statins were found to be efficacious in preventing death and cardiovascular morbidity in people at low cardiovascular risk. Reductions in relative risk were similar to those seen in patients with a history of coronary artery disease.
他汀类药物最初用于改善已确诊冠心病患者的心血管结局,但最近在低心血管风险人群中的使用更为普遍。我们对随机试验进行了系统评价,以评估这些人群中他汀类药物的疗效和危害。
我们检索了 MEDLINE 和 EMBASE(截至 2011 年 1 月 28 日)、卫生技术评估和临床试验登记处以及相关综述的参考文献列表。我们纳入了将低心血管风险的参与者随机分配接受他汀类药物与安慰剂或不接受他汀类药物的试验。我们将低风险定义为观察到的 10 年内心血管相关死亡或非致死性心肌梗死的风险低于 20%,但我们在敏感性分析中探索了其他定义。
我们确定了 29 项符合条件的试验,共涉及 80711 名参与者。接受他汀类药物治疗的患者全因死亡率明显低于对照组(RR 0.90,95%置信区间 [CI] 0.84-0.97),对于心血管疾病 10 年风险<20%的试验[主要分析]和 RR 0.83,95%CI 0.73-0.94,对于 10 年风险<10%的试验[敏感性分析])。他汀类药物组患者发生非致死性心肌梗死(RR 0.64,95%CI 0.49-0.84)和非致死性卒中(RR 0.81,95%CI 0.68-0.96)的可能性也明显低于对照组。荟萃回归和分层分析均未表明高、低效他汀类药物之间的疗效存在统计学差异,或胆固醇降低幅度更大。
他汀类药物在预防低心血管风险人群的死亡和心血管发病率方面是有效的。相对风险的降低与冠心病患者相似。