Lukashevich Valentina, Schweizer Anja, Foley James E, Dickinson Sheila, Groop Per-Henrik, Kothny Wolfgang
Novartis Pharmaceuticals Corporation, East Hanover, NJ 07936-1080, USA.
Vasc Health Risk Manag. 2013;9:21-8. doi: 10.2147/VHRM.S39300. Epub 2013 Jan 23.
The purpose of this study was to evaluate the efficacy of vildagliptin 50 mg once daily in patients with severe renal impairment (estimated glomerular filtration rate < 30 mL/min/1.73 m(2)) and longstanding type 2 diabetes not adequately controlled with insulin therapy, which is a difficult-to-treat population, with limited therapeutic options and a high susceptibility to hypoglycemia.
This was a post hoc subanalysis of data obtained during a previously described randomized, double-blind, parallel-group, 24-week study comparing the efficacy and safety of vildagliptin 50 mg once daily versus placebo in patients with type 2 diabetes and moderate or severe renal impairment. The present data derive from 178 patients with severe renal impairment (baseline estimated glomerular filtration rate approximately 21 mL/min/1.73 m(2), 100 randomized to vildagliptin, 78 randomized to placebo), all of whom were receiving insulin therapy (alone or in combination with an oral antidiabetic agent) for longstanding type 2 diabetes (mean approximately 19 years).
With vildagliptin in combination with insulin, the adjusted mean change (AMΔ) in HbA(1c) from baseline (7.7% ± 0.1%) was -0.9% ± 0.4% and the between-treatment difference (vildagliptin - placebo) was -0.6% ± 0.2% (P < 0.001). The percentage of patients achieving endpoint HbA(1c) < 7.0% was significantly higher with vildagliptin than placebo (45.2% versus 22.8%, P = 0.008). When added to insulin, vildagliptin and placebo had comparable hypoglycemic profiles and did not cause weight gain. Both treatments were similarly well tolerated, with comparable incidences of adverse events, serious adverse events, and deaths.
When added to insulin therapy in patients with severe renal impairment and longstanding type 2 diabetes, vildagliptin 50 mg once daily was efficacious, eliciting HbA(1c) reductions consistent with those previously reported for a patient population with much more recent onset of type 2 diabetes and normal renal function, and had a hypoglycemic profile comparable with placebo. Accordingly, vildagliptin is a suitable treatment option for patients with advanced type 2 diabetes and impaired renal function who require insulin therapy and present a serious therapeutic challenge in clinical practice.
本研究旨在评估每日一次服用50mg维格列汀对严重肾功能损害(估计肾小球滤过率<30mL/min/1.73m²)且长期2型糖尿病患者胰岛素治疗控制不佳的疗效,这是一个治疗困难的群体,治疗选择有限且低血糖易感性高。
这是一项事后亚组分析,数据来自之前描述的一项随机、双盲、平行组、为期24周的研究,该研究比较了每日一次服用50mg维格列汀与安慰剂对2型糖尿病合并中度或重度肾功能损害患者的疗效和安全性。目前的数据来自178例严重肾功能损害患者(基线估计肾小球滤过率约为21mL/min/1.73m²,100例随机接受维格列汀治疗,78例随机接受安慰剂治疗),所有患者均因长期2型糖尿病(平均约19年)接受胰岛素治疗(单独或与口服抗糖尿病药物联合使用)。
维格列汀联合胰岛素治疗时,糖化血红蛋白(HbA1c)从基线(7.7%±0.1%)的调整后平均变化(AMΔ)为-0.9%±0.4%,治疗组间差异(维格列汀-安慰剂)为-0.6%±0.2%(P<0.001)。达到终点糖化血红蛋白<7.0%的患者百分比,维格列汀组显著高于安慰剂组(45.2%对22.8%,P=0.008)。添加到胰岛素治疗中时,维格列汀和安慰剂的低血糖情况相当,且不会导致体重增加。两种治疗的耐受性相似,不良事件、严重不良事件和死亡的发生率相当。
对于严重肾功能损害且长期2型糖尿病患者,在胰岛素治疗基础上加用每日一次50mg维格列汀是有效的,糖化血红蛋白降低程度与之前报道的2型糖尿病发病时间更近且肾功能正常的患者群体一致,并且低血糖情况与安慰剂相当。因此,对于需要胰岛素治疗且在临床实践中面临严重治疗挑战的晚期2型糖尿病和肾功能损害患者,维格列汀是一种合适的治疗选择。