Department of Diabetology, University Hospital Sainte-Marguerite, 270, boulevard de Sainte-Marguerite, 13009 Marseille, France.
Diabetes Metab. 2012 Dec;38(6):507-14. doi: 10.1016/j.diabet.2012.08.010. Epub 2012 Oct 30.
The metabolic efficacy of adding prandial insulin in a stepwise manner to a straightforward basal-bolus regimen was compared in patients with type 2 diabetes mellitus (T2DM), suboptimally controlled by oral antidiabetic drugs (OADs) and once-daily basal insulin.
In this international randomized, parallel-group, non-inferiority study, 811 patients with poorly controlled type 2 diabetes using basal insulin were switched to insulin glargine (GLAR) for 6 months while continuing OADs. Patients with HbA(1c) > 7% and FPG < 120 mg/dL (n=476) were then randomized to either group 1, GLAR+metformin (MET)+3×insulin glulisine (GLU), group 2, GLAR+MET+1-3×GLU, or group 3, GLAR+MET+insulin secretagogue (IS)+1-3×GLU, for 12 months. Objectives were to show the non-inferiority of efficacy of group 2 vs group 1 and vs group 3. Non-inferiority of group 2 vs group 1 was concluded if the upper limit of the 95% confidence interval (CI) for the HbA(1c) difference was ≤ to 0.4%.
The adjusted HbA(1c) difference of group 2 vs 1 for the per-protocol population crossed the non-inferiority margin (0.228, 95% CI: -0.018-0.473). There was significantly less weight gain in group 2 compared with group 1, but adverse events were otherwise similar between the two groups. In patients with HbA(1c) < 8% at baseline, non-inferiority was achieved in group 2 vs group 1.
Although non-inferiority was not achieved, stepwise intensification of GLU added to GLAR showed efficacy close to that of the basal-bolus approach and with significantly less weight gain.
本研究旨在比较在口服降糖药(OADs)和每日一次基础胰岛素治疗血糖控制不佳的 2 型糖尿病(T2DM)患者中,逐步添加餐时胰岛素与直接基础-餐时胰岛素方案相比的代谢疗效。
在这项国际性、随机、平行分组、非劣效性研究中,811 例使用基础胰岛素血糖控制仍不佳的 2 型糖尿病患者换用甘精胰岛素(GLAR)治疗 6 个月,同时继续使用 OADs。HbA1c>7%且 FPG<120mg/dL(n=476)的患者随后随机分为 3 组:第 1 组 GLAR+二甲双胍(MET)+3 次门冬胰岛素(GLU);第 2 组 GLAR+MET+1-3 次 GLU;第 3 组 GLAR+MET+胰岛素促泌剂(IS)+1-3 次 GLU,治疗 12 个月。研究目的是证明第 2 组与第 1 组和第 3 组的疗效非劣效性。如果第 2 组与第 1 组的 HbA1c 差值的 95%置信区间(CI)上限≤0.4%,则可推断第 2 组与第 1 组的非劣效性。
在符合方案人群中,第 2 组与第 1 组的调整后 HbA1c 差值超出了非劣效性边界(0.228,95%CI:-0.018-0.473)。与第 1 组相比,第 2 组体重增加显著较少,但两组间其他不良反应相似。在基线 HbA1c<8%的患者中,第 2 组与第 1 组达到了非劣效性。
尽管未达到非劣效性,但逐步强化 GLU 联合 GLAR 的治疗方案显示出与基础-餐时胰岛素方案相似的疗效,且体重增加显著较少。