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首页> 外文期刊>DMW: Deutsche Medizinische Wochenschrift >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 [Effekt von Dapagliflozin bei Typ-2-Diabetikern mit unzureichender Blutzuckereinstellung unter Glimepirid: Eine randomisierte, 24-w?chige, placebokontrollierte Doppelblindstudie]
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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 [Effekt von Dapagliflozin bei Typ-2-Diabetikern mit unzureichender Blutzuckereinstellung unter Glimepirid: Eine randomisierte, 24-w?chige, placebokontrollierte Doppelblindstudie]

机译:达格列净对格列美脲的血糖控制不足的2型糖尿病患者的影响:一项随机,24周,双盲,安慰剂对照的研究,24周,安慰剂对照的双盲研究]

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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 (HbA 1c) 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.
机译:目的:2型糖尿病(T2DM)中血糖控制的进行性恶化通常需要加强治疗。达格列净通过选择性抑制肾钠-葡萄糖共转运蛋白2(SGLT2)来增加尿葡萄糖排泄。我们评估了格列吡脲加用格列吡嗪对达不到控制的T2DM患者的疗效,安全性和耐受性。方法:这项为期24周,随机,双盲,安慰剂对照,平行组,国际,多中心试验(ClinicalTrials.gov NCT00680745)纳入了接受磺脲类药物治疗的不受控制的T2DM [血红蛋白A1c(HbA 1c)7-10%]的患者单一疗法。成年患者(n = 597)被随机分配给安慰剂或达格列净(2.5、5或10 mg /天),加用开放标签格列美脲4 mg / day,持续24周。主要终点是24周时HbA1c相对于基线的平均变化。次要终点包括体重变化和其他血糖参数。结果:在24周时,安慰剂组与dapagliflozin 2.5 / 5/10 mg组相比于基线的HbA1c调整后平均变化分别为-0.13对-0.58,-0.63,-0.82%(根据Dunnett程序,所有p <0.0001对安慰剂) 。相应的体重和空腹血浆葡萄糖值分别为-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比较,严重不良事件分别为4.8%和6.0-7.1%。低血糖事件4.8对7.1-7.9%;提示生殖器感染的事件为0.7对3.9-6.6%;和提示尿路感染的事件分别为6.2%和3.9-6.9%。没有肾脏感染的报道。结论:在磺脲类单药治疗无法控制的T2DM患者中,将达格列净添加到格列美脲中可显着改善HbA1c,减轻体重,并且通常耐受性好,尽管接受达格列净治疗的患者中生殖器官感染的报道更为频繁。

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