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首页> 外文期刊>Diabetes care >Low-Volume Insulin Degludec 200 Units/mL Once Daily Improves Glycemic Control Similarly to Insulin Glargine With a Low Risk of Hypoglycemia in Insulin-Naive Patients With Type 2 Diabetes: A 26-week, randomized, controlled, multinational, treat-to-target trial: The BEGIN LOW VOLUME trial.
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Low-Volume Insulin Degludec 200 Units/mL Once Daily Improves Glycemic Control Similarly to Insulin Glargine With a Low Risk of Hypoglycemia in Insulin-Naive Patients With Type 2 Diabetes: A 26-week, randomized, controlled, multinational, treat-to-target trial: The BEGIN LOW VOLUME trial.

机译:低体积胰岛素Degludec 200单位/ ml每天一次改善血糖控制,与胰岛素 - 野患者2型糖尿病患者的低血糖风险低,有26周,随机,控制,跨国,治疗到目标 试用:开始低卷试验。

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OBJECTIVE The 200 units/mL formulation of insulin degludec (IDeg 200 units/mL) contains equal units of insulin in half the volume compared with the 100 units/mL formulation. We compared the efficacy and safety of IDeg 200 units/mL once daily with 100 units/mL insulin glargine (IGlar) in insulin-na?ve subjects with type 2 diabetes (T2DM) inadequately controlled with oral antidiabetic drugs. RESEARCH DESIGN AND METHODS In this 26-week, open-label, treat-to-target trial, subjects (n = 457; mean HbA1c 8.3% [67 mmol/mol], BMI 32.4 kg/m(2), and fasting plasma glucose [FPG] 9.6 mmol/L [173.2 mg/dL]) were randomized to IDeg 200 units/mL or IGlar, both given once daily in combination with metformin with or without a dipeptidyl peptidase-4 inhibitor. Basal insulin was initiated at 10 units/day and titrated weekly to an FPG target of <5 mmol/L (<90 mg/dL) according to mean prebreakfast self-measured blood glucose values from the preceding 3 days. RESULTS By 26 weeks, IDeg reduced HbA1c by 1.30% and was not inferior to IGlar. Mean observed FPG reductions were significantly greater with IDeg than IGlar (-3.7 vs. -3.4 mmol/L [-67 vs. -61 mg/dL]; estimated treatment difference: -0.42 [95% CI -0.78 to -0.06], P = 0.02). Despite this difference, rates of overall confirmed hypoglycemia were not higher with IDeg than with IGlar (1.22 and 1.42 episodes/patient-year, respectively), as were rates of nocturnal confirmed hypoglycemia (0.18 and 0.28 episodes/patient-year, respectively). Mean daily basal insulin dose was significantly lower by 11% with IDeg 200 units/mL compared with IGlar. IDeg was well-tolerated, and the rate of treatment-emergent adverse events was similar across groups. CONCLUSIONS In this treat-to-target trial in insulin-na?ve patients with T2DM, IDeg 200 units/mL improved glycemic control similarly to IGlar with a low risk of hypoglycemia.
机译:目的200单位/ mL胰岛素DELLUDEC(IDEG 200单位/ mL)的制剂含有相同单位的胰岛素,其体积的一半与100个单位/ mL配方相比。将IDEG 200单位/ mL每日一次的疗效和安全性与100单位/ mL胰岛素晶粒(Iglar)进行了胰岛素-NAβve,与口腔抗糖尿病药物的2型糖尿病(T2DM)进行了胰岛素-NAαve胰岛素(Iglar)。在本26周,开放标签,治疗到目标试验中的研究设计和方法(n = 457;平均HBA1C 8.3%[67mmol / mol],BMI 32.4kg / m(2),以及空腹等离子体葡萄糖[FPG] 9.6mmol / L [173.2mg / dl]被随机化为IDEG 200单位/ mL或IGLAR,两种与二甲双胍组合给予一次,与二肽基肽酶-4抑制剂组合。基础胰岛素在10个单位/天中引发,并根据前面3天的平均预发育自测自测定血糖值,每周滴定到<5mmol / L(<90mg / dl)的FPG靶标。结果达到26周,IDEG降低了HBA1C的1.30%,不逊色于Iglar。平均观察到的FPG与IDEG的FPG减少比IDEG(-3.7 vs. -3.4mmol / L [-67 vs. -61mm / dl];估计治疗差异:-0.42 [95%CI -0.78至-0.06], p = 0.02)。尽管存在这种差异,但总格的总证实的低恶血症的速率与IDEG不高于IDEG(分别为1.22和1.42集/患者年),夜间确诊的低血糖率(分别为0.18和0.28集/患者年份)。与IGLAR相比,平均每日基础胰岛素剂量与IDEG 200单位/ mL显着降低11%。 IDEG耐受良好,群体局部不良事件的速度相似。结论在胰岛素-NAα患者T2DM患者的这种治疗试验中,IDEG 200单位/ mL改善血糖调查与IGLAR相似,低血糖风险低。

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