General Practice Research Database, Medicines and Healthcare products Regulatory Agency, London, United Kingdom.
PLoS One. 2011;6(12):e28157. doi: 10.1371/journal.pone.0028157. Epub 2011 Dec 2.
To describe the likely extent of confounding in evaluating the risks of cardiovascular (CV) events and mortality in patients using diabetes medication.
The General Practice Research Database was used to identify inception cohorts of insulin and different oral antidiabetics. An analysis of bias and incidence of mortality, acute coronary syndrome, stroke and heart failure were analysed in GPRD, Hospital Episode Statistics and death certificates.
206,940 patients were identified. The bias analysis showed that past thiazolidinedione users had a lower mortality risk compared to past metformin users. There were no differences between past users of rosiglitazone and pioglitazone (adjusted RR of 1.04; 95% CI 0.93-1.18). Current rosiglitazone users had an increased risk of death (adjusted RR 1.20; 95% CI 1.08-1.34) and of hospitalisation for heart failure (adjusted RR of 1.73; 95% CI 1.19-2.51) compared to current pioglitazone users. Risk of mortality was increased two-fold shortly after starting rosiglitazone. Excess risk of death over 3 years with rosiglitazone was 0.3 per 100 in those aged 50-64 years, 2.0 aged 65-74, 3.0 aged 75-84, and 7.0 aged 85+. The cause of death with rosiglitazone was more likely to be due to a disease of the circulatory system.
Higher risks for death (overall and due to cardiovascular disease) and heart failure were found for rosiglitazone compared to pioglitazone. These excess risks were largest in patients aged 65 years or older. The European regulatory decision to suspend rosiglitazone is supported by this study.
描述在评估使用糖尿病药物的患者发生心血管(CV)事件和死亡风险时可能存在的混杂程度。
使用一般实践研究数据库(GPRD)确定胰岛素和不同口服抗糖尿病药物的起始队列。在 GPRD、医院入院统计和死亡证明中分析了偏倚和死亡率、急性冠状动脉综合征、中风和心力衰竭的发生率。
共确定了 206940 名患者。偏倚分析显示,过去使用噻唑烷二酮的患者与过去使用二甲双胍的患者相比,死亡率风险较低。过去使用罗格列酮和吡格列酮的患者之间没有差异(调整后的 RR 为 1.04;95%CI 0.93-1.18)。与当前使用吡格列酮的患者相比,当前使用罗格列酮的患者死亡风险(调整后的 RR 1.20;95%CI 1.08-1.34)和心力衰竭住院风险(调整后的 RR 1.73;95%CI 1.19-2.51)增加。开始使用罗格列酮后不久,死亡率风险增加了两倍。在 50-64 岁年龄组中,罗格列酮使用 3 年内的超额死亡率为每 100 人 0.3,65-74 岁年龄组为 2.0,75-84 岁年龄组为 3.0,85 岁及以上年龄组为 7.0。与罗格列酮相关的死亡原因更可能是循环系统疾病。
与吡格列酮相比,罗格列酮的死亡(总体和心血管疾病导致的死亡)和心力衰竭风险更高。这些超额风险在 65 岁或以上的患者中最大。本研究支持欧洲监管机构暂停罗格列酮的决定。