Garber A J, Foley J E, Banerji M A, Ebeling P, Gudbjörnsdottir S, Camisasca R-P, Couturier A, Baron M A
Baylor College of Medicine, Houston, TX, USA.
Diabetes Obes Metab. 2008 Nov;10(11):1047-56. doi: 10.1111/j.1463-1326.2008.00859.x. Epub 2008 Feb 18.
To compare the efficacy and tolerability of vildagliptin vs. placebo in patients with type 2 diabetes mellitus (T2DM) who are inadequately controlled [haemoglobin A(1c) (HbA(1c)) 7.5 to 11%] with prior sulphonylurea (SU) monotherapy.
This 24-week, multicentre, randomized, double-blind, placebo-controlled study assessed the effects of the dipeptidyl peptidase-4 inhibitor vildagliptin (50 mg given once or twice daily) vs. placebo added to glimepiride (4 mg once daily) in 515 patients with T2DM. Adjusted mean changes from baseline to end-point (AMDelta) in HbA(1c), fasting plasma glucose, fasting lipids and body weight were compared by analysis of covariance.
The between-group difference (vildagliptin - placebo) in AMDelta HbA(1c) was -0.6 +/- 0.1% in patients receiving vildagliptin 50 mg daily and -0.7 +/- 0.1% in those receiving 100 mg daily (p < 0.001 vs. placebo for both). Greater efficacy was seen in patients > or =65 years of age (-0.7 +/- 0.1% and -0.8 +/- 0.2% for 50 and 100 mg daily respectively) and in patients with baseline HbA(1c) > 9% (Delta = -1.0 +/- 0.2% and -0.9 +/- 0.2% for 50 and 100 mg daily respectively). Relative to placebo, patients receiving vildagliptin also had improvements in beta-cell function and postprandial glucose, with small changes in fasting lipids and body weight. The incidences of adverse events (AEs) (67.1, 66.3 and 64.2%) and serious AEs (2.9, 2.4 and 5.1%) were similar in patients receiving 50 mg vildagliptin, 100 mg vildagliptin or placebo respectively. The incidence of hypoglycaemic events was low but slightly higher in the group receiving vildagliptin 100 mg (3.6%) than in the group receiving vildagliptin 50 mg (1.2%) or placebo (0.6%).
In patients with T2DM inadequately controlled with prior SU monotherapy, addition of vildagliptin (50 or 100 mg daily) to glimepiride (4 mg once daily) improves glycaemic control and is well tolerated. Addition of vildagliptin 50 mg daily to SU monotherapy may be a particularly attractive therapy in elderly patients.
比较维格列汀与安慰剂对既往磺脲类药物(SU)单药治疗控制不佳(糖化血红蛋白[HbA(1c)] 7.5%至11%)的2型糖尿病(T2DM)患者的疗效和耐受性。
这项为期24周的多中心、随机、双盲、安慰剂对照研究评估了二肽基肽酶-4抑制剂维格列汀(50 mg每日一次或两次)与添加至格列美脲(4 mg每日一次)的安慰剂对515例T2DM患者的影响。通过协方差分析比较了从基线到终点的糖化血红蛋白、空腹血糖、空腹血脂和体重的调整后平均变化(AMDelta)。
接受每日50 mg维格列汀的患者中,AMDelta糖化血红蛋白的组间差异(维格列汀-安慰剂)为-0.6±0.1%,接受每日100 mg的患者中为-0.7±0.1%(两者与安慰剂相比,p<0.001)。65岁及以上患者(每日50 mg和100 mg分别为-0.7±0.1%和-0.8±0.2%)以及基线糖化血红蛋白>9%的患者(每日50 mg和100 mg分别为Delta=-1.0±0.2%和-0.9±0.2%)疗效更佳。与安慰剂相比,接受维格列汀的患者β细胞功能和餐后血糖也有改善,空腹血脂和体重有小的变化。接受50 mg维格列汀、100 mg维格列汀或安慰剂的患者不良事件(AE)发生率(分别为67.1%、66.3%和64.2%)和严重AE发生率(分别为2.9%、2.4%和5.1%)相似。低血糖事件发生率较低,但接受100 mg维格列汀的组(3.6%)略高于接受50 mg维格列汀的组(1.2%)或安慰剂组(0.6%)。
在既往SU单药治疗控制不佳的T2DM患者中,添加维格列汀(每日50或100 mg)至格列美脲(每日4 mg)可改善血糖控制且耐受性良好。每日添加50 mg维格列汀至SU单药治疗可能对老年患者是一种特别有吸引力的治疗方法。