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阿格列汀治疗日本 2 型糖尿病患者的疗效和安全性:一项随机、双盲、剂量范围比较安慰剂的研究,随后进行长期扩展研究。

Efficacy and safety of alogliptin in Japanese patients with type 2 diabetes mellitus: a randomized, double-blind, dose-ranging comparison with placebo, followed by a long-term extension study.

机构信息

Kansai Electric Power Hospital, Osaka, Japan.

出版信息

Curr Med Res Opin. 2011 Sep;27(9):1781-92. doi: 10.1185/03007995.2011.599371. Epub 2011 Aug 1.

Abstract

OBJECTIVE

To compare the efficacy and safety of different dosages of alogliptin with that of placebo and voglibose in drug-naïve Japanese patients with type 2 diabetes inadequately controlled by diet and exercise.

RESEARCH DESIGN AND METHODS

In the double-blind, placebo-controlled phase of this two-part study, 480 patients aged ≥20 years with type 2 diabetes mellitus (HbA1c ≥6.9% to <10.4%) were randomized to monotherapy with alogliptin 6.25, 12.5, 25 or 50 mg once daily, placebo, or voglibose 0.2 mg three times daily for a period of 12 weeks. In a subsequent open-label, long-term extension phase, patients continued on the same treatment for an additional 40 weeks (patients in the placebo group were reassigned equally to one of the four alogliptin dosages).

MAIN OUTCOME MEASURES

The primary efficacy endpoint was the change in HbA1c from the baseline value at week 12 of treatment. Safety endpoints were the occurrence of adverse events, vital sign measurements, physical examination and ECG findings, and laboratory test results recorded over the entire 52-week period.

RESULTS

HbA1c was dose-dependently reduced by alogliptin, and the changes versus baseline were statistically significant with all four dosages in comparison with both placebo and voglibose. In addition, changes in fasting plasma glucose and postprandial plasma glucose AUC(0-2h) values were significantly greater with all four dosages of alogliptin in comparison with placebo. The incidence of adverse events with alogliptin over 52 weeks was not dose-dependent and was lower than with voglibose. Hypoglycemia occurred infrequently and was generally rated as mild. Changes in body weight with alogliptin were minimal (<0.5 kg) and not clinically meaningful.

CONCLUSIONS

Alogliptin was well tolerated and dose-dependently improved glycemic parameters in patients with type 2 diabetes inadequately controlled on diet and exercise.

摘要

目的

比较不同剂量阿格列汀与安慰剂和伏格列波糖在饮食和运动控制不佳的日本 2 型糖尿病患者中的疗效和安全性。

方法

在这项两部分研究的双盲、安慰剂对照阶段,将 480 名年龄≥20 岁的 2 型糖尿病(HbA1c≥6.9%至<10.4%)患者随机分为阿格列汀 6.25、12.5、25 或 50mg 每日一次、安慰剂或伏格列波糖 0.2mg 每日三次单药治疗,治疗期为 12 周。在随后的开放标签、长期扩展阶段,患者继续接受相同的治疗,另外 40 周(安慰剂组的患者平均分配到阿格列汀的四个剂量组之一)。

主要疗效终点为治疗 12 周时与基线相比 HbA1c 的变化。安全性终点为整个 52 周期间记录的不良事件、生命体征测量、体检和心电图发现以及实验室检查结果。

结果

阿格列汀可剂量依赖性地降低 HbA1c,与安慰剂和伏格列波糖相比,所有四个剂量组与基线相比均有统计学意义。此外,与安慰剂相比,所有四个剂量的阿格列汀均能显著降低空腹血糖和餐后血糖 AUC(0-2h)值。阿格列汀在 52 周内的不良反应发生率与剂量无关,且低于伏格列波糖。低血糖发生频率低,一般为轻度。阿格列汀对体重的影响最小(<0.5kg),且无临床意义。

结论

阿格列汀耐受性良好,可剂量依赖性地改善饮食和运动控制不佳的 2 型糖尿病患者的血糖参数。

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