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Efficacy and hypoglycemic risk of sitagliptin in obese/overweight patients with type 2 diabetes compared with GLP-1 receptor agonists: A meta-analysis

机译:与GLP-1受体激动剂相比,肥胖/超重患者SITAGLIPTIN在肥胖/超重患者中的疗效和低血糖风险:META分析

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Objective: The purpose of this study was to assess the efficacy and hypoglycemic risk of sitagliptin versus that of GLP-1 receptor agonists in the management of obese / overweight patients with T2DM . Methods: EMBASE, PubMed, Cochrane Library, and ClinicalTrials.gov were searched; randomized controlled trials comparing the efficacy of sitagliptin versus that of GLP-1 receptor agonists in obese / overweight patients with T2DM were included. The mean BMI of participants for each study was ≥30 kg/m 2 . We conducted a meta-analysis according to the methods specified in the Cochrane Handbook for Systematic Reviews of Interventions. RevMan 5.1 software was used to perform the meta-analysis . The Cochrane Q test and I 2 statistics were used to estimate the heterogeneity among studies. The results are expressed as the mean difference (MD) or risk ratio (RR) with 95% confidence intervals. Results: A total of 8 eligible studies were included in our meta-analysis . Compared with GLP-1 receptor agonists , sitagliptin was less effective at reducing HbA1c (0.42 [0.27, 0.56]), FPG (0.78 [0.36, 1.19]), PPG (2.61 [1.35, 3.87]), and body weight (1.42 [0.71, 2.14]). Conversely, there were no significant differences in SBP reduction (0.38 [?1.14, 1.89]), DBP reduction (?0.30 [?1.00, 0.39]), and hypoglycemic risk (1.09 [0.50, 2.35]). Conclusion: For obese / overweight patients, sitagliptin may exert a less potent effect on HbA 1C , FPG, PPG, and weight reduction than GLP-1 receptor agonists , but these drugs had a similar efficacy in reducing blood pressure; furthermore, there was no significant difference in hypoglycemic risk .
机译:目的:本研究的目的是评估SITAGLIPTIN与GLP-1受体激动剂在T2DM的肥胖/超重患者管理中的疗效和低血糖风险。方法:研讨,PubMed,Cochrane图书馆和ClinicalTrial.gov被搜查;随机对照试验比较SITAGLIPTIN与GLP-1受体激动剂在肥胖/超重患者中的疗效进行比较。每项研究的参与者的平均BMI≥30kg/ m 2。我们根据Cochrane手册中规定的方法进行了META分析,用于系统性审查的干预措施。 Revman 5.1软件用于执行元分析。 Cochrane Q测试和I 2统计用于估计研究中的异质性。结果表达为平均差异(MD)或风险比(RR),置信间隔95%。结果:我们的META分析中共有8项合格研究。与GLP-1受体激动剂相比,SITAGLIPTIN在还原HBA1C(0.42 [0.27,0.56]),FPG(0.78 [0.36,19]),PPG(2.61 [1.35,3.87])和体重(1.42 [ 0.71,2.14])。相反,SBP减少没有显着差异(0.38 [?1.14,1.89]),DBP减少(?0.30 [?1.00,0.39])和低血糖风险(1.09 [0.50,2.35])。结论:对于肥胖/超重患者,SITAGLIPTIN可能对HBA 1C,FPG,PPG和重量减少效果比GLP-1受体激动剂相似,但这些药物在降低血压方面具有相似的功效;此外,低血糖风险没有显着差异。

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