Saha Sandeep Ajoy, Kizhakepunnur Lenney G, Bahekar Amol, Arora Rohit R
Department of Medicine, Chicago Medical School, Chicago, IL 60064, USA.
Am Heart J. 2007 Nov;154(5):943-53. doi: 10.1016/j.ahj.2007.07.011. Epub 2007 Sep 12.
Fibrates are effective antilipidemic agents with peroxisome proliferator-activated receptor agonist activity, but clinical trial data on their role in cardiovascular prevention are conflicting. We conducted a systematic review and meta-analysis of randomized clinical trials to evaluate their role in prevention of cardiovascular events.
A total of 36,489 patients from 10 published randomized placebo-controlled trials were analyzed using the Mantel-Haenszel fixed-effects model. Odds ratios were computed for cardiovascular outcomes from data pooled from the selected trials, and statistical significance was tested using the z-test statistic (2-sided alpha error <.05).
Fibrates significantly reduced plasma total cholesterol and triglyceride levels by about 8% and 30%, respectively, and raised high-density lipoprotein cholesterol levels by about 9% compared with placebo. The odds of all-cause mortality tended to be higher (P = .08), and the odds of noncardiovascular mortality were significantly higher (P = .004) with the use of fibrates. However, these significant differences did not persist after exclusion of trials using clofibrate as the study drug. Fibrates did not significantly reduce the odds of cardiovascular mortality (P = .68), fatal myocardial infarction (MI) (P = .76), or stroke (P = .56). On the other hand, fibrates significantly reduced the odds of nonfatal MI by about 22% (P < .00001). The odds of developing cancer were not significantly higher with the use of fibrates (P = .98), nor were the odds of cancer-related death (P = .17).
In conclusion, our meta-analysis revealed that the long-term use of fibrates significantly reduces the occurrence of nonfatal MI but has no significant effect on other adverse cardiovascular outcomes.
贝特类药物是具有过氧化物酶体增殖物激活受体激动剂活性的有效抗血脂药物,但关于其在心血管疾病预防中作用的临床试验数据存在矛盾。我们进行了一项随机临床试验的系统评价和荟萃分析,以评估其在预防心血管事件中的作用。
使用Mantel-Haenszel固定效应模型对10项已发表的随机安慰剂对照试验中的36489例患者进行分析。从所选试验汇总的数据中计算心血管结局的比值比,并使用z检验统计量检验统计学显著性(双侧α错误<.05)。
与安慰剂相比,贝特类药物可使血浆总胆固醇和甘油三酯水平分别显著降低约8%和30%,高密度脂蛋白胆固醇水平升高约9%。使用贝特类药物时,全因死亡率的比值倾向于更高(P = .08),非心血管死亡率的比值显著更高(P = .004)。然而,在排除使用氯贝丁酯作为研究药物的试验后,这些显著差异不再存在。贝特类药物并未显著降低心血管死亡率(P = .68)、致命性心肌梗死(MI)(P = .76)或中风(P = .56)的比值。另一方面, 贝特类药物可使非致命性MI的比值显著降低约22%(P < .00001)。使用贝特类药物时,患癌的比值没有显著升高(P = .98),癌症相关死亡的比值也没有显著升高(P = .17)。
总之,我们的荟萃分析表明,长期使用贝特类药物可显著降低非致命性MI的发生率,但对其他不良心血管结局没有显著影响。