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首页> 外文期刊>Pharmacoepidemiology and drug safety >Use of thiazolidinediones and risk of osteoporotic fracture: disease or drugs?
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Use of thiazolidinediones and risk of osteoporotic fracture: disease or drugs?

机译:使用噻唑烷反对剂和骨质疏松骨折的风险:疾病或毒品?

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Clinical and observational studies suggest that use of thiazolidinediones (TZDs) is associated with an increased fracture risk. In addition, type 2 diabetes mellitus (T2DM) is a risk factor for osteoporotic fracture. Our aim was to estimate fracture risks in TZD users and users of other antidiabetic drugs, classified according to proxies of disease severity.We conducted a population-based cohort study utilizing the Dutch PHARMO database (1998-2008). PHARMO links pharmacy-dispensing data to the National Hospital Registry. Oral antidiabetic users (n = 123,452) were matched 1:4 by year of birth and sex to non-users. Cox proportional hazards models were used to estimate hazard ratios (HRs) of fracture in TZD users. We created a proxy indicator for disease severity. The first stage was defined as current use of either a biguanide or a sulfonylureum, the second stage as current use of a biguanide and a sulfonylureum at the same time, the third stage was assigned to patients using TZDs and the fourth stage to patients using insulin.The risk of osteoporotic fracture was increased 1.5-fold (HR 1.49, 95%CI 1.28-1.73) in patients who currently used TZDs (stage 3), and for patients using insulin (stage 4), the risk was increased 1.2-fold (HR 1.24, 1.14-1.36), as compared with controls. In the first and second stages, risks were lower: HR 1.11 (1.06-1.17) for stage 1 and HR 1.03 (0.96-1.11) for stage 2.When observational studies assess risk of fracture in patients with TZDs, the severity of T2DM should be taken into account.
机译:临床和观察性研究表明,使用噻唑烷二酮(TZDS)与骨折风险增加有关。此外,2型糖尿病(T2DM)是骨质疏松骨折的危险因素。我们的宗旨是估算TZD用户和其他抗糖尿病药物的骨折风险,根据疾病严重性的代理进行分类。我们进行了利用荷兰药物数据库(1998-2008)的基于人口的队列研究。 Pharmo将药房分配数据链接到国家医院登记处。口腔反对药物(N = 123,452)与出生年份和性别与非用户匹配1:4。 Cox比例危险模型用于估算TZD用户中骨折的危险比(HRS)。我们为疾病严重创建了代理指标。第一阶段定义为目前使用双胍或磺酰化,第二阶段作为目前使用双胍和磺酰化的同时,将第三阶段分配给使用胰岛素的患者使用TZD和第四阶段的患者分配给患者。骨质疏松骨折的风险增加1.5倍(HR 1.49,95%CI 1.28-1.73),目前使用TZDS(第3阶段),以及使用胰岛素(第4阶段)的患者,风险增加1.2倍(HR 1.24,1.14-1.36),与对照相比。在第一阶段和第二个阶段,阶段1和HR 1.11(1.06-1.17)的风险降低(1.06-1.17),适用于阶段的2阶段和HR 1.03(0.96-1.11)。观察研究的观察研究评估患者患者骨折的风险时,T2DM的严重程度应该是被考虑在内。

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