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Randomized controlled clinical trial of a combination therapy of vildagliptin plus an α-glucosidase inhibitor for patients with type II diabetes mellitus

机译:维格列汀联合α-葡萄糖苷酶抑制剂联合治疗II型糖尿病的随机对照临床试验

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摘要

The aim of this study was to assess the efficacy of a combination therapy of vildagliptin plus an α-glucosidase inhibitor for patients with type II diabetes mellitus. Type II diabetic patients exhibiting poor glycemic control following α-glucosidase inhibitor treatment for at least two months were selected and randomly distributed into vildagliptin and placebo groups. The body weight, fasting blood glucose (FBG), postprandial glucose (PPG), glycated hemoglobin (HBA1c) and blood lipid levels and hepatorenal functions of the patients were determined before and 12 weeks after the trial. Following the trial, the FBG, PPG, HbA1c, cholesterol (CHOL) and triglyceride (TG) levels in the vildagliptin group were significantly decreased compared with the pretreatment levels (P<0.05), whereas only the PPG level in the placebo group decreased (P<0.05). The FBG, PPG and HbA1c levels in the vildagliptin group were markedly lower than those in the placebo group 12 weeks after the trial. A comparison of the body weights and hepatorenal functions before and after the trial or between groups did not show statistically significant differences. The combination therapy of vildagliptin plus an α-glucosidase inhibitor effectively reduced the FBG, PPG and HbA1c levels in patients without inducing weight gain or hepatorenal dysfunction. However, the therapy may have caused a reduction in the blood lipid levels.
机译:这项研究的目的是评估维格列汀联合α-葡萄糖苷酶抑制剂对II型糖尿病患者的疗效。选择经α-葡萄糖苷酶抑制剂治疗至少两个月后血糖控制不佳的II型糖尿病患者,随机分为维格列汀和安慰剂组。在试验前和试验后12周确定患者的体重,空腹血糖(FBG),餐后血糖(PPG),糖化血红蛋白(HBA1c),血脂水平和肝肾功能。试验后,维格列汀组的FBG,PPG,HbA1c,胆固醇(CHOL)和甘油三酸酯(TG)水平与治疗前水平相比显着降低(P <0.05),而安慰剂组中只有PPG水平降低( P <0.05)。试验后12周,维达列汀组的FBG,PPG和HbA1c水平明显低于安慰剂组。试验前后或各组之间体重和肝肾功能的比较未显示统计学上的显着差异。维格列汀与α-葡萄糖苷酶抑制剂的联合治疗可有效降低患者的FBG,PPG和HbA1c水平,而不会引起体重增加或肝肾功能不全。但是,该疗法可能导致血脂水平降低。

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