Shih Chia-Jen, Chen Hung-Ta, Kuo Shu-Chen, Ou Shuo-Ming, Chen Yung-Tai
School of Medicine, National Yang-Ming University, Taipei, Taiwan; Department of Medicine, Taipei Veterans General Hospital, Yuanshan Branch, Yilan, Taiwan.
School of Medicine, National Yang-Ming University, Taipei, Taiwan; Division of Endocrinology and Metabolism, Department of Medicine, Taipei City Hospital, Heping Fuyou Branch, Taipei, Taiwan.
J Am Med Dir Assoc. 2016 Jan;17(1):59-64. doi: 10.1016/j.jamda.2015.10.009. Epub 2015 Nov 21.
The elderly (aged ≥65 years) population with type 2 diabetes (T2D) is growing substantially, but evidence for associations between the use of dipeptidyl peptidase-4 inhibitors (DPP-4is), novel incretin-based antidiabetic drugs, and clinical hard endpoints in this group remains inconclusive. We aimed to assess the safety and cardiovascular effects of DPP-4i use in a nationally representative sample of elderly adults with T2D.
DESIGN, SETTING, AND PARTICIPANTS: We conducted a nationwide, observational, propensity score-matched study using Taiwan's National Health Insurance Research Database. Of a total of 414,213 patients aged ≥65 years with T2D, 58,485 patients receiving initial DPP-4i prescriptions between March 1, 2009, and June 31, 2013, were included. Each DPP-4i user was matched with a nonuser control using propensity scores. The endpoints were all-cause mortality and major adverse cardiovascular events (MACEs), including ischemic stroke and myocardial infarction. Potential adverse effects of hospitalization for heart failure and hypoglycemia were also evaluated.
Compared with the matched control cohort, the risks of all-cause mortality (hazard ratio [HR] 0.54, 95% confidence interval [CI] 0.52-0.56), MACEs (HR 0.79, 95% CI 0.75-0.83), myocardial infarction (HR 0.79, 95% CI 0.72-0.87), and ischemic stroke (HR 0.79, 95% CI 0.75-0.84) were lower in the DPP-4i cohort. DPP-4i use did not affect the risks of hospitalization for heart failure and hypoglycemia. Stratified analyses produced consistent results across age, sex, and comorbidity subgroups.
Prescription of DPP-4is was associated with reduced risks of all-cause mortality and MACEs in patients aged ≥65 years with T2D.
老年(年龄≥65岁)2型糖尿病(T2D)患者数量正在大幅增长,但二肽基肽酶-4抑制剂(DPP-4i)(新型基于肠促胰岛素的抗糖尿病药物)的使用与该组患者临床硬终点之间关联的证据仍不确凿。我们旨在评估在全国具有代表性的老年T2D成人样本中使用DPP-4i的安全性和心血管效应。
设计、背景和参与者:我们利用台湾地区国民健康保险研究数据库进行了一项全国性的观察性倾向评分匹配研究。在总共414213例年龄≥65岁的T2D患者中,纳入了2009年3月1日至2013年6月31日期间首次接受DPP-4i处方的58485例患者。使用倾向评分将每位DPP-4i使用者与未使用者对照进行匹配。终点为全因死亡率和主要不良心血管事件(MACE),包括缺血性卒中和心肌梗死。还评估了因心力衰竭和低血糖住院的潜在不良反应。
与匹配的对照队列相比,DPP-4i队列中的全因死亡率(风险比[HR]0.54,95%置信区间[CI]0.52 - 0.56)、MACE(HR 0.79,95%CI 0.75 - 0.83)、心肌梗死(HR 0.79,95%CI 0.72 - 0.87)和缺血性卒中(HR 0.79,95%CI 0.75 - 0.84)风险较低。使用DPP-4i不影响因心力衰竭和低血糖住院的风险。分层分析在年龄、性别和合并症亚组中产生了一致的结果。
在年龄≥65岁的T2D患者中,开具DPP-4i与降低全因死亡率和MACE风险相关。