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首页> 外文期刊>Endocrine journal >Comparative analysis of the effects of alogliptin and vildagliptin on glucose metabolism in type 2 diabetes mellitus
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Comparative analysis of the effects of alogliptin and vildagliptin on glucose metabolism in type 2 diabetes mellitus

机译:阿格列汀和维格列汀对2型糖尿病患者葡萄糖代谢影响的比较分析

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The aim of this 24-week, prospective randomized open-label study was to compare the effects of alogliptin and vildagliptin on glucose control, renal function, and lipid metabolism. In Study 1, DPP-4 inhibitor-naive type 2 diabetes (T2DM) were randomly assigned to alogliptin 25 mg/day or vildagliptin 50 mg twice daily. In Study 2, T2DM on treatment with 50 mg/day sitagliptin were switched to either 25 mg/day alogliptin or 50 mg twice daily vildagliptin. The primary endpoint was change in glycosylated hemoglobin (HbA1c) level at 24 weeks, while the secondary endpoints were changes in urinary albumin excretion and low-density lipoprotein cholesterol (LDL-C) levels at 24 weeks. In Study 1, HbA1c levels changed at 24-week by -0.5±0.7% in the alogliptin group (p=0.002, relative to baseline) and -0.7±0.9% in the vildagliptin group (p=0.001, relative to baseline), and the extent of these changes were comparable between the two groups (p=0.219). The decrease in log urinary albumin excretion was more significant in the vildagliptin group (p=0.008). In Study 2, HbA1c levels at 24-week changed by 0.2±0.7% in the switch-to-alogliptin group (p=0.007) and 0.0±0.6% in the switch-to-vildagliptin group (p=0.188), indicating a significant difference between the groups (p=0.003). In both studies, the changes in LDL-C levels were comparable between the two groups. The two drugs had comparable glucose-lowering effects in DPP-4 inhibitor-naive patients but the effect was more pronounced for vildagliptin in patients switched from sitagliptin. The results may point to subtle yet important differences between the two DPP-4 inhibitors. This trial was registered with UMIN (no. #000019022).
机译:这项为期24周的前瞻性随机开放标签研究旨在比较阿格列汀和维格列汀对血糖控制,肾功能和脂质代谢的影响。在研究1中,将DPP-4初治型2型糖尿病(T2DM)随机分配给阿格列汀25 mg /天或维达列汀50 mg每天两次。在研究2中,将使用50 mg /天西他列汀治疗的T2DM改为25 mg /天阿格列汀或50 mg每日两次维格列汀。主要终点是24周时糖基化血红蛋白(HbA1c)水平的变化,而次要终点是24周时尿白蛋白排泄和低密度脂蛋白胆固醇(LDL-C)水平的变化。在研究1中,阿格列汀组的HbA1c水平在24周时变化了-0.5±0.7%(相对于基线,p = 0.002)和维格列汀组的相对于基线(p = 0.001)的-0.7±0.9%,这些变化的程度在两组之间是可比的(p = 0.219)。维格列汀组对数尿白蛋白排泄的减少更为显着(p = 0.008)。在研究2中,转用阿格列汀组(p = 0.007)在24周时的HbA1c水平变化了0.2±0.7%,而转用维格列汀组(p = 0.188)则变化了0.0±0.6%。两组之间的差异显着(p = 0.003)。在两项研究中,两组之间的LDL-C水平变化均相当。两种药物在未使用DPP-4抑制剂的患者中具有相当的降糖效果,但对于维他列汀从西他列汀治疗的患者,这种作用更为明显。结果可能表明两种DPP-4抑制剂之间存在细微但重要的差异。该试验已在UMIN注册(编号#000019022)。

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