Tan Xinrui, Pan Xiongfeng, Wu Xiaochuan, Zheng Songjia, Chen Yuyao, Liu Donghai, Zhang Xingxing
Department of Pediatrics, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Department of Epidemiology and Health Statistics, Xiangya School of Public Health, Central South University, Changsha, Hunan, China.
Front Pharmacol. 2023 Mar 16;14:975880. doi: 10.3389/fphar.2023.975880. eCollection 2023.
To assess the efficacy and safety of glucagon-like peptide-1 receptor agonists (GLP-1 RAs) used as an adjunct to insulin therapy in adults with type 1 diabetes. A search of electronic databases (Medline, Embase, and the Cochrane Central Register of Controlled Trials) from 1 January 1950 to 23 May 2021 was conducted to find randomized controlled trials. The primary outcome was the change in HbA1c. Eight efficacy and six safety secondary endpoints were evaluated meta-analysis. Weighted mean difference (WMD) and odds ratio (OR), alongside 95% confidence interval (CI), were calculated using the random effects model. Among 1,379 candidate studies, 11 trials comprising 2,856 participants satisfied the inclusion criteria. Overall, GLP-1 RA adjunctive therapy reduced HbA1c by -0.21% (95% CI, -0.33 to -0.10), weight by -4.04 kg (-4.8 to -3.27), systolic pressure by -2.57 mmHg (-4.11 to -1.03), and diastolic blood pressure by -1.02 mmHg (-1.99 to -0.06). In addition, there was a decrease in prandial insulin dose (WMD, -4.23 IU; 95% CI, -5.26 to -3.20), basal insulin dose (-2.40 IU; -3.93 to -0.87), and total insulin dose (-5.73 IU; -10.61 to -0.86). Moreover, GLP-1 RAs did not increase the incidence of severe hypoglycemia, diabetic ketoacidosis, or severe adverse events. However, GLP-1 RAs increased the incidence of gastrointestinal adverse events (OR, 2.96; 95% CI, 2.33-3.77). Our meta-analysis of randomized clinical trials suggests moderate beneficial effects of GLP-1 RAs on the metabolic profile in patients with type 1 diabetes, without an increased risk of serious adverse events. https://www.crd.york.ac.uk/PROSPERO; Identifier: CRD 42020199840.
评估胰高血糖素样肽-1受体激动剂(GLP-1 RAs)作为胰岛素治疗辅助药物用于1型糖尿病成人患者的疗效和安全性。检索了1950年1月1日至2021年5月23日的电子数据库(Medline、Embase和Cochrane对照试验中央注册库)以查找随机对照试验。主要结局是糖化血红蛋白(HbA1c)的变化。通过荟萃分析评估了8个疗效次要终点和6个安全性次要终点。使用随机效应模型计算加权平均差(WMD)和比值比(OR)以及95%置信区间(CI)。在1379项候选研究中,11项试验(共2856名参与者)符合纳入标准。总体而言,GLP-1 RA辅助治疗使HbA1c降低了-0.21%(95%CI,-0.33至-0.10),体重降低了-4.04千克(-4.8至-3.27),收缩压降低了-2.57毫米汞柱(-4.11至-1.03),舒张压降低了-1.02毫米汞柱(-1.99至-0.06)。此外,餐时胰岛素剂量(WMD,-4.23国际单位;95%CI,-5.26至-3.20)、基础胰岛素剂量(-2.40国际单位;-3.93至-0.87)和总胰岛素剂量(-5.73国际单位;-10.61至-0.86)均有所降低。此外,GLP-1 RAs并未增加严重低血糖、糖尿病酮症酸中毒或严重不良事件的发生率。然而,GLP-1 RAs增加了胃肠道不良事件的发生率(OR,2.96;95%CI,2.33 - 3.77)。我们对随机临床试验的荟萃分析表明,GLP-1 RAs对1型糖尿病患者的代谢状况有适度有益影响,且不会增加严重不良事件的风险。https://www.crd.york.ac.uk/PROSPERO;标识符:CRD 42020199840。