Jeon Won Kyeong, Kang Jeehoon, Kim Hyo-Soo, Park Kyung Woo
Department of Internal Medicine and Cardiovascular Center, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea.
J Lipid Atheroscler. 2021 May;10(2):210-222. doi: 10.12997/jla.2021.10.2.210. Epub 2021 Jan 25.
Recent studies have raised concern about the cardiovascular safety of dipeptidyl peptidase-4 (DPP4) inhibitors. We performed a systematic review through meta-analysis to compare cardiovascular outcomes of sulfonylurea (SU) versus DPP4 inhibitors when used in combination with metformin.
After searching for trials using combination therapy of metformin with DPP4 inhibitor or SU in PubMed, Cochrane Library, and Embase, one prospective observation study and 15 randomized controlled studies were selected.
Regarding the primary analysis endpoint, there were no significant differences in the risk of all-cause mortality between SU and DPP4 inhibitors as an add-on therapy to metformin (random-effect relative risk [RR], 1.14; 95% confidence interval [CI], 0.98-1.33; =0.811; I=0%). Cardiovascular death was also similar between the two drug classes in the five studies which reported outcomes (random-effect RR, 1.03; 95% CI, 0.83-1.27; =0.517; I=0%). Furthermore, there were no significant differences in major adverse cardiac events (MACE), coronary heart disease, myocardial infarction, ischemic stroke and heart failure. However, there were less hypoglycemic events and weight gain in the DPP4 inhibitor group as compared with the SU group (random-effect RR, 3.79; 95% CI, 1.53-9.39; <0.001; I=98.2 and weighted mean difference, 1.68; 95% CI, 1.07-2.29; <0.001; I=94.7, respectively).
As add-on therapy to metformin, there were no significant differences in all-cause mortality and cardiovascular mortality between DPP4 inhibitors and SUs.
近期研究引发了对二肽基肽酶-4(DPP4)抑制剂心血管安全性的关注。我们通过荟萃分析进行了一项系统评价,以比较磺脲类药物(SU)与DPP4抑制剂联合二甲双胍使用时的心血管结局。
在PubMed、Cochrane图书馆和Embase中检索使用二甲双胍与DPP4抑制剂或SU联合治疗的试验后,选取了1项前瞻性观察研究和15项随机对照研究。
关于主要分析终点,作为二甲双胍的附加治疗,SU和DPP4抑制剂在全因死亡率风险方面无显著差异(随机效应相对风险[RR],1.14;95%置信区间[CI],0.98 - 1.33;P = 0.811;I² = 0%)。在报告了结局的5项研究中,这两类药物的心血管死亡情况也相似(随机效应RR,1.03;95% CI,0.83 - 1.27;P = 0.517;I² = 0%)。此外,在主要不良心脏事件(MACE)、冠心病、心肌梗死、缺血性卒中和心力衰竭方面无显著差异。然而,与SU组相比,DPP4抑制剂组的低血糖事件和体重增加较少(随机效应RR,3.79;95% CI,1.53 - 9.39;P < 0.001;I² = 98.2%,加权平均差,1.68;95% CI,1.07 - 2.29;P < 0.001;I² = 94.7%,分别)。
作为二甲双胍的附加治疗,DPP4抑制剂和SU在全因死亡率和心血管死亡率方面无显著差异。