Division of Endocrinology and Metabolism, Department of Internal Medicine, Ditmanson Medical Foundation Chiayi Christian Hospital, Chiayi City, Taiwan.
College of Chinese Medicine, China Medical University, Taichung, Taiwan.
Diabetologia. 2018 Mar;61(3):562-573. doi: 10.1007/s00125-017-4499-5. Epub 2017 Nov 14.
AIMS/HYPOTHESIS: The effect of pioglitazone was compared with that of other second-line glucose-lowering drugs on the risk of dementia among individuals with type 2 diabetes receiving metformin-based dual therapy.
A total of 204,323 individuals with type 2 diabetes aged ≥18 years who were stable metformin users and dementia-free before the initiation of second-line glucose-lowering medication were identified in the period 2000-2011 from Taiwan's National Health Insurance Research Database and followed to the end of 2013. Primary analyses included 51,415 individuals aged ≥65 years without dementia events in the first year of second-line glucose-lowering treatment. Study subjects were classified into mutually exclusive groups according to various second-line glucose-lowering drugs to metformin. Cox proportional hazards models were applied to assess the time-to-event between propensity score-matched glucose-lowering treatment groups.
Individuals aged ≥65 years on metformin + pioglitazone had a significantly lower risk of dementia compared with those on metformin + sulfonylurea (HR 0.56; 95% CI 0.34, 0.93), and a lower, but insignificant, risk of dementia compared with those on other metformin-based dual regimens (i.e. metformin + acarbose, metformin + meglitinide, metformin + insulin or metformin + dipeptidyl peptidase 4 inhibitors). Among individuals aged ≥18 years, there was also a decreased risk of dementia in those taking pioglitazone compared with those taking other second-line glucose-lowering drugs. A lower incidence of dementia was found in users of metformin + pioglitazone compared with users of metformin + rosiglitazone.
CONCLUSIONS/INTERPRETATION: Pioglitazone as a second-line treatment after metformin might provide a protective effect on dementia risk among individuals with type 2 diabetes.
目的/假设:本研究旨在比较吡格列酮与其他二线降糖药物在二甲双胍双联疗法基础上治疗 2 型糖尿病患者的痴呆风险。
本研究纳入了 204323 名年龄≥18 岁、接受二甲双胍双联疗法且在开始使用二线降糖药物前无痴呆的稳定二甲双胍使用者,这些患者均来自 2000 年至 2011 年台湾全民健康保险研究数据库,并随访至 2013 年底。主要分析纳入了 51415 名在二线降糖治疗的第一年无痴呆事件发生的年龄≥65 岁的患者。研究对象根据各种二线降糖药物与二甲双胍的相互排斥分组,采用 Cox 比例风险模型评估倾向评分匹配的降糖治疗组之间的时间事件。
与二甲双胍+磺酰脲类(HR 0.56;95%CI 0.34,0.93)相比,年龄≥65 岁的患者服用二甲双胍+吡格列酮治疗痴呆的风险显著降低,与其他基于二甲双胍的双联方案(即二甲双胍+阿卡波糖、二甲双胍+格列奈类、二甲双胍+胰岛素或二甲双胍+二肽基肽酶-4 抑制剂)相比,痴呆风险虽有所降低,但无统计学意义。在年龄≥18 岁的患者中,与服用其他二线降糖药物的患者相比,服用吡格列酮的患者痴呆风险也有所降低。与服用二甲双胍+罗格列酮的患者相比,服用二甲双胍+吡格列酮的患者痴呆发生率较低。
结论/解释:二甲双胍双联疗法后使用吡格列酮可能对 2 型糖尿病患者的痴呆风险有保护作用。