Walker Alexander M, Koro Carol E, Landon Joan
World Health Information Science Consultants LLC, Wellesley, MA 02481, USA.
Pharmacoepidemiol Drug Saf. 2008 Aug;17(8):760-8. doi: 10.1002/pds.1598.
The risk of coronary heart disease (CHD) in users of antidiabetic agents must be quantified to permit reasoned therapeutic choices.
To assess the risk of myocardial infarction (MI) and coronary revascularization (CR), in diabetic patients who began rosiglitazone, pioglitazone, metformin, or sulfonylureas.
We conducted a retrospective cohort study of MI and CR in the PharMetrics database. We performed head-to-head comparisons using propensity-score-stratified Cox proportional hazards models, examining risks both on-treatment and during total follow-up before regimen switches.
For the combined outcome (MI and CR), the crude rates per 1000 person years were 9 on monotherapy, 13 on dual therapy, and 21 on therapies combined with insulin. In the absence of insulin, regimens containing thiazolidinediones (TZDs) tended toward lower risk than comparable regimens containing sulfonylureas and higher risk than those containing metformin. The summary hazard ratio for rosiglitazone versus pioglitazone was 1.04 (95%CI: 0.94-1.14) for total follow-up and 1.05 (0.92-1.19) for on-treatment time. For MI, the hazard ratios were 1.07 (0.89-1.27) for total follow-up and 1.21 (0.95-1.54) for on-treatment time.
The present data indicate that the risk of CHD in patients using TZDs appears to lie between the risks associated with sulfonylureas and metformin. Neither the risk of MI and CR together nor the risk of MI alone was significantly different between rosiglitazone and pioglitazone. A nonsignificant observed excess risk of 21% for MI during on-treatment time will require combination with the results of other studies to provide a reliable assessment.
必须对使用抗糖尿病药物的患者患冠心病(CHD)的风险进行量化,以便做出合理的治疗选择。
评估开始使用罗格列酮、吡格列酮、二甲双胍或磺脲类药物的糖尿病患者发生心肌梗死(MI)和冠状动脉血运重建(CR)的风险。
我们在PharMetrics数据库中对MI和CR进行了一项回顾性队列研究。我们使用倾向评分分层的Cox比例风险模型进行直接比较,检查治疗期间和治疗方案转换前的总随访期间的风险。
对于联合结局(MI和CR),每1000人年的粗发病率在单药治疗时为9,双联治疗时为13,与胰岛素联合治疗时为21。在不使用胰岛素的情况下,含噻唑烷二酮类(TZDs)的治疗方案的风险往往低于含磺脲类的可比治疗方案,高于含二甲双胍的治疗方案。罗格列酮与吡格列酮的总随访汇总风险比为1.04(95%CI:0.94 - 1.14),治疗期间为1.05(0.92 - 1.19)。对于MI,总随访的风险比为1.07(0.89 - 1.27),治疗期间为1.21(0.95 - 1.54)。
目前的数据表明,使用TZDs的患者患CHD的风险似乎介于与磺脲类和二甲双胍相关的风险之间。罗格列酮和吡格列酮在MI和CR联合风险或单独MI风险方面均无显著差异。治疗期间观察到的MI风险非显著额外增加21%,需要与其他研究结果相结合以提供可靠评估。