首页> 美国卫生研究院文献>Journal of Drug Assessment >Vildagliptin efficacy in combination with metformin among Jordanian patients with type 2 diabetes mellitus inadequately controlled with metformin
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Vildagliptin efficacy in combination with metformin among Jordanian patients with type 2 diabetes mellitus inadequately controlled with metformin

机译:维达列汀与二甲双胍联合治疗对二甲双胍控制不足的约旦2型糖尿病患者的疗效

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摘要

>Objective >: To assess the efficacy and safety of vildagliptin added to metformin in patients with type 2 diabetes mellitus (T2DM) inadequately controlled with metformin monotherapy. >Methods: This was a 12-week prospective observational study where vildagliptin 50 mg twice daily was added to patients with T2DM inadequately controlled (glycosylated hemoglobin type A1c (Hba1c) 7–10%) by a daily dose of metformin ≥1700 mg between June 2012 and May 2013. Efficacy was assessed by change in Hba1c and fasting plasma glucose (FPG) levels, and safety was assessed by reported adverse events (AEs). >Results: A total of 58 patients were enrolled in this study. Their age ranged between 39.0 and 71.0 years, with a mean of 52.6 years, and a standard deviation (SD) of 7.8. The average duration of diabetes mellitus (DM) was 4.0 years (SD 3.0) and half of the patients have had DM for more than three years. The mean baseline levels of Hba1c and FPG were 8% and 10.8 mmol/L, respectively. Patients treated with vildagliptin achieved clinically significant reductions in Hba1c of 1.1% (p value <.005) and reduction in FPG of 1.8 mmol/L (p value <.005) from baseline. Overall, 62.1% had achieved the target of Hba1c of <7% after vildagliptin use. Greater reductions in Hba1c were linked to higher baseline levels as well as to the daily frequency of metformin use. Mild AEs were reported by 16 patients. There was no incidence of hypoglycemia and there were no significant changes in body weight after treatment. >Conclusions: Vildagliptin as add-on therapy to metformin improved glycemic control and was highly tolerable in T2DM patients who were inadequately controlled by metformin monotherapy.
机译:>目的 >::评估在二甲双胍单药治疗不能充分控制的2型糖尿病(T2DM)患者中,将维达列汀添加到二甲双胍中的疗效和安全性。 >方法:这是一项为期12周的前瞻性观察性研究,每天以2剂量的剂量将维达列汀50 mg每日两次加至控制不充分的2型糖化血红蛋白(A1c型糖化血红蛋白(Hba1c)7-10%)的T2DM患者中在2012年6月至2013年5月期间,二甲双胍≥1700μmg。通过Hba1c和空腹血糖(FPG)水平的变化评估疗效,并通过报告的不良事件(AE)评估安全性。 >结果:该研究共纳入58位患者。他们的年龄介于39.0至71.0岁之间,平均年龄为52.6岁,标准差(SD)为7.8。糖尿病(DM)的平均持续时间为4.0年(SD 3.0),一半的患者患有DM超过三年。 Hba1c和FPG的平均基线水平分别为8%和10.8 mmol / L。维格列汀治疗的患者与基线相比,Hba1c临床上显着降低了1.1%(p值<.005),FPG降低了1.8 mmol / L(p值<.005)。总体而言,使用维格列汀后,有62.1%的Hba1c达到了<7%的目标。 Hba1c的更大降低与更高的基线水平以及二甲双胍的每日使用频率有关。 16例患者报告有轻度不良事件。治疗后无低血糖发生,体重也无明显变化。 >结论:维达列汀作为二甲双胍的辅助治疗可改善血糖控制,并且在二甲双胍单药治疗不能充分控制的T2DM患者中高度耐受。

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