Nissen Steven E, Wolski Kathy
Department of Cardiovascular Medicine, Cleveland Clinic, Cleveland, OH 44195, USA.
N Engl J Med. 2007 Jun 14;356(24):2457-71. doi: 10.1056/NEJMoa072761. Epub 2007 May 21.
Rosiglitazone is widely used to treat patients with type 2 diabetes mellitus, but its effect on cardiovascular morbidity and mortality has not been determined.
We conducted searches of the published literature, the Web site of the Food and Drug Administration, and a clinical-trials registry maintained by the drug manufacturer (GlaxoSmithKline). Criteria for inclusion in our meta-analysis included a study duration of more than 24 weeks, the use of a randomized control group not receiving rosiglitazone, and the availability of outcome data for myocardial infarction and death from cardiovascular causes. Of 116 potentially relevant studies, 42 trials met the inclusion criteria. We tabulated all occurrences of myocardial infarction and death from cardiovascular causes.
Data were combined by means of a fixed-effects model. In the 42 trials, the mean age of the subjects was approximately 56 years, and the mean baseline glycated hemoglobin level was approximately 8.2%. In the rosiglitazone group, as compared with the control group, the odds ratio for myocardial infarction was 1.43 (95% confidence interval [CI], 1.03 to 1.98; P=0.03), and the odds ratio for death from cardiovascular causes was 1.64 (95% CI, 0.98 to 2.74; P=0.06).
Rosiglitazone was associated with a significant increase in the risk of myocardial infarction and with an increase in the risk of death from cardiovascular causes that had borderline significance. Our study was limited by a lack of access to original source data, which would have enabled time-to-event analysis. Despite these limitations, patients and providers should consider the potential for serious adverse cardiovascular effects of treatment with rosiglitazone for type 2 diabetes.
罗格列酮被广泛用于治疗2型糖尿病患者,但其对心血管疾病发病率和死亡率的影响尚未确定。
我们检索了已发表的文献、美国食品药品监督管理局的网站以及药品制造商(葛兰素史克)维护的临床试验注册库。纳入我们荟萃分析的标准包括研究持续时间超过24周、使用未接受罗格列酮的随机对照组以及有心肌梗死和心血管原因死亡的结局数据。在116项可能相关的研究中,42项试验符合纳入标准。我们将所有心肌梗死和心血管原因死亡的病例进行了列表统计。
采用固定效应模型合并数据。在42项试验中,受试者的平均年龄约为56岁,平均基线糖化血红蛋白水平约为8.2%。与对照组相比,罗格列酮组心肌梗死的比值比为1.43(95%置信区间[CI],1.03至1.98;P = 0.03),心血管原因死亡的比值比为1.64(95%CI,0.98至2.74;P = 0.06)。
罗格列酮与心肌梗死风险的显著增加以及心血管原因死亡风险的增加相关,后者具有临界显著性。我们的研究因无法获取原始数据而受限,否则本可进行事件发生时间分析。尽管有这些局限性,患者和医疗服务提供者应考虑罗格列酮治疗2型糖尿病可能产生的严重心血管不良影响。