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胰岛素德谷胰岛素/门冬胰岛素与门冬胰岛素 30 治疗未经控制的、胰岛素治疗的 2 型糖尿病的比较:一项 3a 期、随机、靶向治疗的试验。

Comparison of insulin degludec/insulin aspart and biphasic insulin aspart 30 in uncontrolled, insulin-treated type 2 diabetes: a phase 3a, randomized, treat-to-target trial.

机构信息

University of Sydney, Royal North Shore Hospital, Australia

Aarhus University Hospital, Aarhus, Denmark.

出版信息

Diabetes Care. 2014 Aug;37(8):2084-90. doi: 10.2337/dc13-2908. Epub 2014 May 8.

Abstract

OBJECTIVE

Insulin degludec/insulin aspart (IDegAsp) is the first combination of a basal insulin with an ultralong duration of action, and a rapid-acting insulin in a single injection. This trial compared IDegAsp with biphasic insulin aspart 30 (BIAsp 30) in adults with type 2 diabetes inadequately controlled with once- or twice-daily (OD or BID) pre- or self-mixed insulin with or without oral antidiabetic drugs.

RESEARCH DESIGN AND METHODS

In this 26-week, randomized, open-label, multinational, treat-to-target trial, participants (mean age 58.7 years, duration of diabetes 13 years, BMI 29.3 kg/m(2), and HbA1c 8.4% [68 mmol/mol]) were exposed (1:1) to BID injections of IDegAsp (n = 224) or BIAsp 30 (n = 222), administered with breakfast and the main evening meal and dose titrated to a self-measured premeal plasma glucose (PG) target of 4.0-5.0 mmol/L.

RESULTS

After 26 weeks, mean HbA1c was 7.1% (54 mmol/mol) for both groups, with IDegAsp achieving the prespecified noninferiority margin for mean change in HbA1c (estimated treatment difference [ETD] -0.03% points [95% CI -0.18 to 0.13]). Treatment with IDegAsp was superior in lowering fasting PG (ETD -1.14 mmol/L [95% CI -1.53 to -0.76], P < 0.001) and had a significantly lower final mean daily insulin dose (estimated rate ratio 0.89 [95% CI 0.83-0.96], P = 0.002). Fewer confirmed, nocturnal confirmed, and severe hypoglycemia episodes were reported for IDegAsp compared with BIAsp 30.

CONCLUSIONS

IDegAsp BID effectively improves HbA1c and fasting PG levels with fewer hypoglycemia episodes versus BIAsp 30 in patients with uncontrolled type 2 diabetes previously treated with once- or twice-daily pre- or self-mixed insulin.

摘要

目的

德谷胰岛素/门冬胰岛素(IDegAsp)是首个将基础胰岛素与超长效作用时间、速效胰岛素结合在单支注射笔中的药物。本试验旨在比较德谷胰岛素和预混胰岛素类似物 30(BIAsp 30)在接受一次或两次/每日(OD 或 BID)预混或自我混合胰岛素治疗、或联合使用口服降糖药治疗后血糖仍控制不佳的 2 型糖尿病患者中的疗效。

研究设计和方法

这是一项为期 26 周、随机、开放标签、多国、以目标为导向的试验,参与者(平均年龄 58.7 岁,糖尿病病程 13 年,BMI 29.3kg/m2,HbA1c 8.4%[68mmol/mol])按 1:1 比例分别接受德谷胰岛素 BID(n=224)或 BIAsp 30 BID(n=222)治疗,早餐和主餐时注射,根据自我监测的餐前血浆葡萄糖(PG)目标(4.0-5.0mmol/L)调整剂量。

结果

26 周后,两组的平均 HbA1c 均为 7.1%(54mmol/mol),德谷胰岛素达到了 HbA1c 平均变化的预设非劣效性边界(估计治疗差异[ETD]-0.03%,95%CI-0.18 至 0.13)。德谷胰岛素在降低空腹 PG 方面表现更优(ETD-1.14mmol/L,95%CI-1.53 至-0.76,P<0.001),且最终平均日胰岛素剂量显著降低(估计率比 0.89,95%CI0.83-0.96,P=0.002)。与 BIAsp 30 相比,德谷胰岛素治疗组报告的确诊、夜间确诊和严重低血糖事件更少。

结论

与 BIAsp 30 相比,德谷胰岛素 BID 可有效改善血糖控制,降低 HbA1c 和空腹 PG 水平,且低血糖事件更少,适用于接受一次或两次/每日预混或自我混合胰岛素治疗后血糖控制仍不佳的 2 型糖尿病患者。

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