Starke Paula, Thürmann Petra, Grobe Thomas, Friede Tim, Mathes Tim
Department of Medical Statistics, University Medical Center Göttingen, Göttingen, Germany.
Clinical Pharmacology, Faculty of Health, University of Witten/Herdecke, Witten, Germany.
Drugs Aging. 2025 Jun 10. doi: 10.1007/s40266-025-01218-0.
This study complements evidence from randomized controlled trials on the harms (e.g., hypoglycemia) of sulfonylureas compared with dipeptidyl peptidase-4 inhibitors (DPP4i) in the treatment of type 2 diabetes in older adults using real-world data. Existing evidence suggests an increased risk of hypoglycemia, falls, fractures, and cardiovascular events.
Using target trial emulation, we analyzed a retrospective cohort drawn from German routine claims data. We included patients older than 65 years who initiated DPP4i (sitagliptin, vildagliptin, or saxagliptin) or sulfonylureas (glibenclamid or glimepirid) as add on to metformin between 2011 and 2018. Confounding was adjusted for through overlap weighting, and the average treatment effects were estimated in the overlap population using generalized linear models.
Among 171,318 eligible patients, 111,865 (65%) received DPP4i and 59,453 (35%) sulfonylureas. Patients treated with DPP4i had a higher prevalence of all observed comorbidities. Applying overlap weights to adjust for confounding, patients treated with DPP4i had a higher rate of combined all-cause hospitalizations and outpatient visits compared with those treated with sulfonylureas (rate ratio = 1.03, 95% CI 1.02-1.03) in the total population. In contrast, we found a protective effect of DPP4i on the risk for severe hypoglycemia in the subgroups of new users (ratio rate (RR) = 0.51, 95% CI 0.33, 0.76) and patients with severe renal insufficiency (RR = 0.31, 95% CI 0.16, 0.61).
Deprescribing sulfonylureas and using DPP4i instead may slightly reduce harm in some subgroups of older adults, which supports recommendations of existing lists of potentially inappropriate medications.
本研究利用真实世界数据,补充了关于在老年2型糖尿病患者治疗中,磺脲类药物与二肽基肽酶-4抑制剂(DPP4i)相比的危害(如低血糖)的随机对照试验证据。现有证据表明低血糖、跌倒、骨折和心血管事件的风险增加。
使用目标试验模拟,我们分析了从德国常规索赔数据中提取的回顾性队列。我们纳入了2011年至2018年间开始使用DPP4i(西他列汀、维格列汀或沙格列汀)或磺脲类药物(格列本脲或格列美脲)作为二甲双胍附加治疗的65岁以上患者。通过重叠加权调整混杂因素,并使用广义线性模型在重叠人群中估计平均治疗效果。
在171,318名符合条件的患者中,111,865名(65%)接受了DPP4i治疗,59,453名(35%)接受了磺脲类药物治疗。接受DPP4i治疗的患者所有观察到的合并症患病率更高。应用重叠权重调整混杂因素后,在总体人群中,接受DPP4i治疗的患者与接受磺脲类药物治疗的患者相比,全因住院和门诊就诊的综合发生率更高(发生率比=1.03,95%CI 1.02-1.03)。相比之下,我们发现DPP4i对新使用者亚组(比率率(RR)=0.51,95%CI 0.33,0.76)和严重肾功能不全患者(RR=0.31,95%CI 0.16,0.61)的严重低血糖风险有保护作用。
停用磺脲类药物而改用DPP4i可能会在一些老年亚组中轻微减少危害,这支持了现有潜在不适当药物清单的建议。