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:低剂量地高胰岛素Degludec 200单位/ mL每日一次可改善血糖控制,与初治2型糖尿病患者低血糖风险低的胰岛素甘精胰岛素相似:为期26周,随机,对照,多国,针对性治疗试用:BEGIN LOW VOLUME试用。

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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 mg / mL地格列酮胰岛素制剂(IDeg 200单位/ mL)与100单位/ mL制剂相比,胰岛素的等体积单位为一半。我们比较了每天口服200毫克/毫升IDeg与100毫升/ mL甘精胰岛素(IGlar)的有效性和安全性,这些研究对象是未经口服抗糖尿病药控制不充分的未接受胰岛素治疗的2型糖尿病(T2DM)受试者。研究设计和方法在这个为期26周的开放性,靶向治疗试验中,受试者(n = 457;平均HbA1c 8.3%[67 mmol / mol],BMI 32.4 kg / m(2)和空腹血浆葡萄糖(FPG)9.6 mmol / L [173.2 mg / dL])随机分配至IDeg 200单位/ mL或IGlar,均与二甲双胍联合使用,每天加或不加二肽基肽酶-4抑制剂。基础胰岛素以每天10单位的剂量开始,并根据前3天的早餐前自行测量的平均血糖值,每周滴定至<5 mmol / L(<90 mg / dL)的FPG目标。结果到26周时,IDeg可使HbA1c降低1.30%,且不低于IGlar。 IDeg的平均观察到的FPG降低明显高于IGlar(-3.7对-3.4 mmol / L [-67对-61 mg / 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IDeg的总体确诊低血糖发生率并不比IGlar高(分别为1.22和1.42次/患者/年),以及夜间确诊的低血糖发生率(分别为0.18和0.28 /患者/年)。与IGlar相比,IDeg 200单位/ mL的平均每日基础胰岛素剂量显着降低11%。 IDeg具有良好的耐受性,各组之间的治疗紧急不良事件发生率相似。结论在这项针对初治T2DM的胰岛素初治患者的治疗目标试验中,IDeg 200单位/ mL与低血糖风险低的IGlar相似,改善了血糖控制。

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