Dimitrios Patoulias, Michael Doumas, Vasilios Kotsis, Konstantinos Stavropoulos, Konstantinos Imprialos, Ioanna Zografou, Konstantinos Petidis, Spyridon Bakatselos, Asterios Karagiannis
Second Propedeutic Department of Internal Medicine, General Hospital "Hippokration", Aristotle University of Thessaloniki, Thessaloniki, Greece.
VAMC and George Washington University, Washington, DC, United States.
Curr Diabetes Rev. 2020;16(4):313-326. doi: 10.2174/1573399815666190614141918.
A few Randomized Controlled Trials (RCTs) have evaluated the use of liraglutide in Type 1 Diabetes (T1D). Through the present systematic review and meta-analysis, we aim at critically appraising and summarizing those RCTs, providing precise effect estimates.
We searched major databases and grey literature from their inception to October 2018, for RCTs with a duration ≥ 12 weeks, comparing liraglutide with placebo or any other comparator as adjunct to insulin in patients with T1D, investigating major efficacy and safety endpoints. This review is reported in accordance with the Preferred Reporting Items for Systematic reviews and Meta-Analyses (PRISMA) statement.
We included 5 trials with 2,445 randomized participants. Liraglutide provided modest reductions in HbA1c, with liraglutide 1.8 mg producing the greatest decrease (MD = -0.24%, 95% CI -0.32 to -0.16, I2=0%). Significant weight reduction, up to 4.87 kg with liraglutide 1.8 mg was also observed (95% CI -5.31 to -4.43, I2=0%). Decrease in total daily insulin dose, primarily driven by a decrease in bolus insulin requirements, was demonstrated. Liraglutide decreased non-significantly the odds for severe hypoglycemia (OR=0.80, 95% CI 0.57-1.14, I2=0%), while it increased significantly the odds for gastrointestinal adverse events (for nausea, OR=4.70, 95% CI 3.68-6.00, I2=37%, and for vomiting, OR=2.50, 95% CI 1.54-4.72, I2=27%). A significant increase in heart rate was also demonstrated. No association with diabetic ketoacidosis or malignancies was identified.
In patients with T1D, liraglutide might prove be an adjunct to insulin, improving glycemic control, inducing body weight loss and decreasing exogenous insulin requirements and severe hypoglycemia.
少数随机对照试验(RCT)评估了利拉鲁肽在1型糖尿病(T1D)中的应用。通过本系统评价和荟萃分析,我们旨在严格评估和总结这些RCT,提供精确的效应估计值。
我们检索了主要数据库和灰色文献,时间跨度从创建至2018年10月,查找持续时间≥12周的RCT,比较利拉鲁肽与安慰剂或任何其他对照物作为T1D患者胰岛素辅助治疗的效果,研究主要疗效和安全性终点。本评价按照系统评价和荟萃分析的首选报告项目(PRISMA)声明进行报告。
我们纳入了5项试验,共2445名随机参与者。利拉鲁肽可适度降低糖化血红蛋白(HbA1c),其中1.8mg利拉鲁肽降低幅度最大(MD=-0.24%,95%CI -0.32至-0.16,I2=0%)。还观察到显著的体重减轻,1.8mg利拉鲁肽减重可达4.87kg(95%CI -5.31至-4.43,I2=0%)。证实每日总胰岛素剂量减少,主要是由于推注胰岛素需求减少。利拉鲁肽使严重低血糖的几率非显著降低(OR=0.80,95%CI 0.57-1.14,I2=0%),而胃肠道不良事件的几率显著增加(恶心的OR=4.70,95%CI 3.68-6.00,I2=37%;呕吐的OR=2.50,95%CI 1.54-4.72,I2=27%)。还证实心率显著增加。未发现与糖尿病酮症酸中毒或恶性肿瘤有关联。
在T1D患者中,利拉鲁肽可能是胰岛素的辅助治疗药物,可改善血糖控制、减轻体重、减少外源性胰岛素需求及严重低血糖的发生。