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Efficacy and safety of liraglutide monotherapy compared with metformin in Japanese overweight/obese patients with type 2 diabetes

机译:利拉鲁肽单药联合二甲双胍治疗日本超重/肥胖2型糖尿病的疗效和安全性

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References(41) Cited-By(5) There is little information on direct comparison between metformin and glucagon-like peptide-1 (GLP-1) receptor agonists in the Asian population. This study examined the efficacy and safety of liraglutide monotherapy compared with metformin monotherapy in overweight/obese Japanese patients with type 2 diabetes (T2DM). The study was a 24-week, open-labeled, randomized controlled study. Overweight or obese patients with T2DM aged 20-75 years with suboptimal glycemic control were randomized to liraglutide or metformin monotherapy. The primary endpoint was change in HbA1c at week 24. Secondary endpoints included changes in daily glycemic profile, body weight, incidence of hypoglycemia and other adverse events. The study, which was originally planned to enroll 50 subjects in each group, was ended with insufficient recruitment. A total of 46 subjects completed the study, and analysis was conducted in this cohort. Reduction in HbA1c at week 24 was comparable between the metformin (n = 24) and liraglutide (n = 22) groups (-0.95 ± 0.80% vs. -0.80 ± 0.88%, p = 0.77), while the liraglutide group reached maximal reduction more rapidly than did the metformin group. There was no significant difference in weight gain or incidence of hypoglycemia between the groups. Diarrhea was more frequent in the metformin group, while constipation was more frequent in the liraglutide group. There was no significant difference in treatment satisfaction between the groups. In conclusion, liraglutide and metformin monotherapy showed similar reduction in HbA1c during 24 weeks, with no difference in weight gain or incidence of hypoglycemia in overweight or obese Japanese patients with T2DM.
机译:参考文献(41)被引用的人(5)在亚洲人群中,关于二甲双胍和胰高血糖素样肽-1(GLP-1)受体激动剂之间直接比较的信息很少。这项研究检查了利拉鲁肽单药治疗与二甲双胍单药治疗在超重/肥胖日本2型糖尿病(T2DM)患者中的疗效和安全性。该研究是一项为期24周,开放标签的随机对照研究。年龄在20-75岁之间,血糖控制不佳的超重或肥胖T2DM患者被随机分为利拉鲁肽或二甲双胍单药治疗。主要终点为第24周时HbA1c的变化。次要终点为每日血糖曲线,体重,低血糖发生率和其他不良事件的变化。该研究原计划每组招募50名受试者,但由于招募不足而结束。共有46名受试者完成了研究,并在该队列中进行了分析。二甲双胍(n = 24)和利拉鲁肽(n = 22)组在第24周时HbA1c的减少相当(-0.95±0.80%对-0.80±0.88%,p = 0.77),而利拉鲁肽组达到最大减少比二甲双胍组更快。两组之间体重增加或低血糖发生率无显着差异。二甲双胍组的腹泻频率更高,而利拉鲁肽组的便秘频率更高。两组之间的治疗满意度无明显差异。总之,利拉鲁肽和二甲双胍单药治疗在24周内HbA1c的降低相似,在体重过重或肥胖的日本T2DM患者中,体重增加或低血糖发生率无差异。

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