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Hospitalised hip fracture risk with rosiglitazone and pioglitazone use compared with other glucose-lowering drugs

机译:与其他降糖药相比,使用罗格列酮和吡格列酮可导致住院的髋部骨折风险

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摘要

Aims/hypothesis Current drug labels for thiazolidinediones (TZDs) warn of increased fractures, predominantly for distal fractures in women. We examined whether exposure to TZDs affects hip fracture in women and men and compared the risk to that found with other drugs used in diabetes. Methods Using a nationwide database of prescriptions, hospital admissions and deaths in those with type 2 diabetes in Scotland we calculated TZD exposure among 206,672 individuals. Discrete-time failure analysis was used to model the effect of cumulative drug exposure on hip fracture during 1999-2008. Results There were 176 hip fractures among 37,479 exposed individuals. Hip fracture risk increased with cumulative exposure to TZD: OR per year of exposure 1.18 (95% CI 1.09, 1.28; p=3×10 ), adjusted for age, sex and calendar month. Hip fracture increased with cumulative exposure in both men (OR 1.20; 95% CI 1.03, 1.41) and women (OR 1.18; 95% CI 1.07, 1.29) and risks were similar for pioglitazone (OR 1.18) and rosiglitazone (OR 1.16). The association was similar when adjusted for exposure to other drugs for diabetes and for other potential confounders. There was no association of hip fracture with cumulative exposure to sulfonylureas, metformin or insulin in this analysis. The 90-day mortality associated with hip fractures was similar in ever-users of TZD (15%) and in never-users (13%). Conclusions/interpretation Hip fracture is a severe adverse effect with TZDs, affecting both sexes; labels should be changed to warn of this. The excess mortality is at least as much as expected from the reported association of pioglitazone with bladder cancer.
机译:目的/假设噻唑烷二酮类药物(TZDs)的当前药物标签警告增加的骨折,主要是女性远端骨折。我们检查了暴露于TZDs是否会影响男女的髋部骨折,并将其风险与糖尿病中使用的其他药物的风险进行了比较。方法使用全国性的处方药,住院治疗和苏格兰2型糖尿病患者死亡数据库,我们计算了206,672个人的TZD暴露。离散时间失效分析用于模拟1999-2008年间累积药物暴露对髋部骨折的影响。结果37479例暴露者中有176例髋部骨折。髋部骨折的风险随着TZD的累积暴露而增加:或每年暴露1.18(95%CI 1.09,1.28; p = 3×10),并根据年龄,性别和日历月进行了调整。髋部骨折随着男性(OR 1.20; 95%CI 1.03,1.41)和女性(OR 1.18; 95%CI 1.07,1.29)的累积暴露而增加,吡格列酮(OR 1.18)和罗格列酮(OR 1.16)的风险相似。调整为其他药物治疗糖尿病和其他潜在混杂因素后的关联性相似。在此分析中,髋部骨折与磺酰脲类,二甲双胍或胰岛素的累积暴露无关联。髋关节骨折相关的90天死亡率在长期使用TZD的患者中为15%,从未使用过的患者为13%。结论/解释髋部骨折是TZDs的严重不良反应,影响男女。标签应更改以发出警告。超额死亡率至少与吡格列酮与膀胱癌的相关报道所预期的死亡率相同。

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