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在二甲双胍控制不佳的 2 型糖尿病患者中,西格列汀或格列吡嗪治疗的安全性和疗效:一项为期 2 年的研究。

Safety and efficacy of treatment with sitagliptin or glipizide in patients with type 2 diabetes inadequately controlled on metformin: a 2-year study.

机构信息

Merck Research Laboratories, Rahway, NJ, USA.

出版信息

Int J Clin Pract. 2010 Apr;64(5):562-76. doi: 10.1111/j.1742-1241.2010.02353.x.

Abstract

OBJECTIVES

To evaluate the 2-year safety and efficacy of adding sitagliptin or glipizide to ongoing metformin in patients with type 2 diabetes.

METHODS

Patients who were on a stable dose of metformin (> or = 1500 mg/day) for at least 8 weeks were randomised in a double-blind manner to receive either sitagliptin 100 mg q.d. (N = 588) or glipizide 5 mg/day (up-titrated up to 20 mg/day based upon prespecified glycaemic criteria) (N = 584). The efficacy analysis assessed the change in HbA(1c) from baseline using the per-protocol (PP) population.

RESULTS

For the PP cohort, mean baseline HbA(1c) was 7.3% in both groups. After 2 years, the least squares (LS) mean change in HbA(1c) from baseline [95% confidence interval (CI)] was -0.54% (-0.64, -0.45) with sitagliptin (n = 248) and -0.51% (-0.60, -0.42) with glipizide (n = 256). The rise in HbA(1c) from week 24 to week 104 [i.e. coefficient of durability (COD)] was smaller with sitagliptin [COD (95% CI) 0.16%/year (0.10, 0.21)] compared with glipizide [0.26%/year (0.21, 0.31)]. The proportion of patients with an HbA(1c)< 7% was 63% and 59% with sitagliptin and glipizide, respectively. The beta-cell responsiveness to a meal challenge was maintained with sitagliptin and decreased with glipizide. The proportion of patients who reported hypoglycaemia was 5% with sitagliptin and 34% with glipizide [difference in proportions (95% CI) = -29% (-33, -25)]. Relative to baseline, sitagliptin was associated with weight loss (-1.6 kg) compared with weight gain (+0.7 kg) with glipizide.

CONCLUSION

In patients with type 2 diabetes, adding sitagliptin to metformin monotherapy improved glycaemic control over 2 years, similar to the glucose-lowering efficacy observed with adding glipizide, but with greater durability and generally better maintenance of beta-cell function. Sitagliptin was generally well tolerated with a lower risk of hypoglycaemia and weight loss compared with weight gain observed with glipizide.

摘要

目的

评估在接受二甲双胍治疗的 2 型糖尿病患者中加用西他列汀或格列吡嗪的 2 年安全性和疗效。

方法

至少服用 8 周稳定剂量(≥1500mg/天)的二甲双胍的患者,以双盲方式随机接受西他列汀 100mg qd(N=588)或格列吡嗪 5mg/天(根据预先指定的血糖标准滴定至 20mg/天)(N=584)。疗效分析采用符合方案(PP)人群评估了从基线开始的 HbA1c 变化。

结果

对于 PP 队列,两组的平均基线 HbA1c 为 7.3%。2 年后,西他列汀(n=248)的 LS 均值 HbA1c 变化较基线下降-0.54%(-0.64,-0.45),格列吡嗪(n=256)为-0.51%(-0.60,-0.42)。与格列吡嗪相比,西他列汀的 HbA1c 升高幅度(即耐久性系数 COD)从第 24 周到第 104 周较小[0.16%/年(0.10,0.21)](COD(95%CI)0.26%/年(0.21,0.31))。HbA1c<7%的患者比例分别为西他列汀组 63%和格列吡嗪组 59%。餐挑战后β细胞的反应性在西他列汀治疗后保持,而在格列吡嗪治疗后下降。报告低血糖的患者比例分别为西他列汀组 5%和格列吡嗪组 34%(差异比例(95%CI)=-29%(-33,-25))。与基线相比,西他列汀与格列吡嗪相比,体重减轻(-1.6kg),而体重增加(+0.7kg)。

结论

在 2 型糖尿病患者中,加用西他列汀治疗二甲双胍单药治疗可改善 2 年血糖控制,疗效与加用格列吡嗪相似,但耐久性更好,β细胞功能通常更好地维持。与格列吡嗪相比,西他列汀耐受性较好,低血糖风险较低,体重减轻而不是体重增加。

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