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达格列净治疗格列美脲控制不佳的 2 型糖尿病患者的疗效:一项随机、24 周、双盲、安慰剂对照试验。

Effect of dapagliflozin in patients with type 2 diabetes who have inadequate glycaemic control with glimepiride: a randomized, 24-week, double-blind, placebo-controlled trial.

机构信息

Department of Internal Diseases, Diabetology and Nephrology, Silesian Medical University, Zabrze, Poland.

出版信息

Diabetes Obes Metab. 2011 Oct;13(10):928-38. doi: 10.1111/j.1463-1326.2011.01434.x.

Abstract

AIMS

Progressive deterioration of glycaemic control in type 2 diabetes mellitus (T2DM) often requires treatment intensification. Dapagliflozin increases urinary glucose excretion by selective inhibition of renal sodium-glucose cotransporter 2 (SGLT2). We assessed the efficacy, safety and tolerability of dapagliflozin added to glimepiride in patients with uncontrolled T2DM.

METHODS

This 24-week, randomized, double-blind, placebo-controlled, parallel-group, international, multicentre trial (ClinicalTrials.gov NCT00680745) enrolled patients with uncontrolled T2DM [haemoglobin A1c (HbA1c) 7-10%] receiving sulphonylurea monotherapy. Adult patients (n = 597) were randomly assigned to placebo or dapagliflozin (2.5, 5 or 10 mg/day) added to open-label glimepiride 4 mg/day for 24 weeks. Primary endpoint was HbA1c mean change from baseline at 24 weeks. Secondary endpoints included change in body weight and other glycaemic parameters.

RESULTS

At 24 weeks, HbA1c adjusted mean changes from baseline for placebo versus dapagliflozin 2.5/5/10 mg groups were -0.13 versus -0.58, -0.63, -0.82%, respectively (all p < 0.0001 vs. placebo by Dunnett's procedure). Corresponding body weight and fasting plasma glucose values were -0.72, -1.18, -1.56, -2.26 kg and -0.11, -0.93, -1.18, -1.58 mmol/l, respectively. In placebo versus dapagliflozin groups, serious adverse events were 4.8 versus 6.0-7.1%; hypoglycaemic events 4.8 versus 7.1-7.9%; events suggestive of genital infection 0.7 versus 3.9-6.6%; and events suggestive of urinary tract infection 6.2 versus 3.9-6.9%. No kidney infections were reported.

CONCLUSIONS

Dapagliflozin added to glimepiride in patients with T2DM uncontrolled on sulphonylurea monotherapy significantly improved HbA1c, reduced weight and was generally well tolerated, although events suggestive of genital infections were reported more often in patients receiving dapagliflozin.

摘要

目的

2 型糖尿病(T2DM)患者的血糖控制逐渐恶化通常需要强化治疗。达格列净通过选择性抑制肾脏钠-葡萄糖共转运蛋白 2(SGLT2)来增加尿糖排泄。我们评估了达格列净联合格列美脲治疗血糖控制不佳的 T2DM 患者的疗效、安全性和耐受性。

方法

这是一项为期 24 周、随机、双盲、安慰剂对照、平行分组、国际性、多中心试验(ClinicalTrials.gov NCT00680745),纳入了正在接受磺酰脲类单药治疗且血糖控制不佳(糖化血红蛋白 [HbA1c] 7-10%)的 T2DM 患者。成年患者(n=597)按 1:1:1:1 的比例随机分为安慰剂组或达格列净 2.5、5 或 10 mg/天组,联合开放标签格列美脲 4 mg/天治疗 24 周。主要终点为 24 周时 HbA1c 自基线的平均变化。次要终点包括体重和其他血糖参数的变化。

结果

24 周时,安慰剂组与达格列净 2.5/5/10 mg 组的 HbA1c 自基线的调整均值变化分别为-0.13%与-0.58%、-0.63%、-0.82%(所有 P<0.0001 与安慰剂相比,Dunnett 检验)。相应的体重和空腹血糖值分别为-0.72、-1.18、-1.56、-2.26kg 和-0.11、-0.93、-1.18、-1.58mmol/L。安慰剂组与达格列净组的严重不良事件发生率分别为 4.8%与 6.0%-7.1%;低血糖事件发生率分别为 4.8%与 7.1%-7.9%;疑似生殖器感染的事件发生率分别为 0.7%与 3.9%-6.6%;疑似尿路感染的事件发生率分别为 6.2%与 3.9%-6.9%。未报告肾脏感染。

结论

在接受磺酰脲类单药治疗血糖控制不佳的 T2DM 患者中,达格列净联合格列美脲治疗可显著改善 HbA1c,减轻体重,且通常具有良好的耐受性,尽管接受达格列净治疗的患者报告了更多疑似生殖器感染的事件。

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