Yang Jin, Tian Qing, Tang Yuexin, Shah Arvind K, Zhang Ruya, Chen Guojuan, Zhang Ye, Rajpathak Swapnil, Hong Tianpei
Department of Endocrinology and Metabolism, Peking University Third Hospital, Beijing, China.
MRL, Merck & Co., Inc., Kenilworth, NJ, USA.
Diabetes Ther. 2020 Oct;11(10):2371-2382. doi: 10.1007/s13300-020-00914-x. Epub 2020 Sep 2.
To evaluate the efficacy and safety of dipeptidyl peptidase 4 inhibitors (DPP4i) used in combination with insulin in patients with type 2 diabetes mellitus (T2DM).
We searched the MEDLINE, Embase, and Cochrane library databases for randomized controlled trials (RCTs) published through June 2018. Studies with at least a 12-week treatment period were included to compare the addition of DPP4i to insulin with insulin control therapy. Meanwhile, groups on a stable insulin dosage (insulin-stable subgroup) or titrating insulin dosage (insulin-flexible subgroup) were analyzed separately.
Twenty-one RCTs with 3697 patients randomized to a DPP4i/insulin treatment arm and 3538 to an insulin control arm were included. DPP4i, when added to insulin therapy, led to a significantly greater reduction in HbA1c (- 0.57%, 95% CI - 0.66, - 0.48) and provided significantly greater odds of achieving the HbA1c target < 7% (OR 3.45; 95% CI 2.58, 4.63). These effects were achieved in the context of a decrease in the daily insulin requirement, without increases in hypoglycemia risk and body weight, compared with the control treatment. Subgroup analysis showed control-adjusted reductions in HbA1c from baseline in the insulin-stable subgroup (- 0.64%; 95% CI - 0.74, - 0.53) and the insulin-flexible subgroup (- 0.43%; 95% CI - 0.56, - 0.30). Other results occurred similarly in both subgroups.
The addition of DPP4i to insulin is associated with a statistically significant reduction in glycemic control as measured by HbA1c, fasting plasma glucose, and 2-h postprandial glucose, without increasing the risk of hypoglycemia and weight gain. These conclusions were also observed in both stable-dose and flexible-dose insulin subgroups.
评估二肽基肽酶4抑制剂(DPP4i)与胰岛素联合应用于2型糖尿病(T2DM)患者的疗效和安全性。
检索MEDLINE、Embase和Cochrane图书馆数据库,查找截至2018年6月发表的随机对照试验(RCT)。纳入治疗期至少为12周的研究,以比较在胰岛素治疗基础上加用DPP4i与胰岛素对照治疗的效果。同时,分别分析胰岛素剂量稳定组(胰岛素稳定亚组)和胰岛素剂量滴定组(胰岛素灵活亚组)。
纳入21项RCT,共3697例患者随机分配至DPP4i/胰岛素治疗组,3538例患者分配至胰岛素对照组。在胰岛素治疗中加用DPP4i可使糖化血红蛋白(HbA1c)显著降低(-0.57%,95%可信区间-0.66,-0.48),并使达到HbA1c目标值<7%的几率显著增加(比值比3.45;95%可信区间2.58,4.63)。与对照治疗相比,在每日胰岛素需求量减少的情况下取得了这些效果,且低血糖风险和体重均未增加。亚组分析显示,胰岛素稳定亚组(-0.64%;95%可信区间-0.74,-0.53)和胰岛素灵活亚组(-0.43%;95%可信区间-0.56,-0.30)从基线开始经对照调整后的HbA1c均降低。两个亚组的其他结果相似。
在胰岛素治疗基础上加用DPP4i可使糖化血红蛋白、空腹血糖和餐后2小时血糖所衡量的血糖控制情况在统计学上显著改善,且不增加低血糖风险和体重增加风险。在胰岛素稳定剂量组和灵活剂量组中均观察到了这些结论。