Malone J K, Woodworth J R, Arora V, Yang H, Campaigne B N, Hallé J P, Yale J F, Grossman L D
Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, Indiana 46285, USA.
Clin Ther. 2000 Feb;22(2):222-30. doi: 10.1016/s0149-2918(00)88480-5.
This double-blind study was designed to compare the postprandial glucodynamic profile of Humalog Mix75/25, a new premixed insulin analogue containing 75% neutral protamine lispro and 25% insulin lispro with that of human insulin 70/30 (70% neutral protamine Hagedorn insulin and 30% regular human insulin) in patients with type 2 diabetes mellitus.
Insulin lispro Mix75/25 (Mix75/25) is the first available insulin formulation in which both the rapid-acting and basal components are insulin analogues.
This randomized, multicenter, double-blind, crossover study monitored patients' postprandial glucodynamic response to Mix75/25 and human insulin 70/30 (70/30) after a standard test meal. Eighty-four patients with type 2 diabetes participated in this study and were randomly assigned to 1 of 2 treatment sequence groups. Patients received an identical test meal on 4 occasions, completing 2 test meals for each treatment. Equal doses of Mix75/25 or 70/30 were administered 5 minutes before each of the 2 test meals, with doses individualized for each patient. Blood samples were collected for 4 hours after the meal for measurement of plasma glucose. From these plasma glucose measurements, fasting plasma glucose, 2-hour postprandial glucose (2pp), 2-hour postprandial glucose excursion (2pp(ex)), maximum glucose excursion (Gex(max)), the area under the glucose concentration versus time curve from 0 to 4 hours (AUC4), and the area under the glucose excursion versus time curve from 0 to 4 hours (AUCex4) were calculated.
Because of significant differences in the baseline fasting plasma glucose levels between Mix75/25 and 70/30 (Mix75/25: 8.9+/-2.2 mmol/L [160.2+/-39.6 mg/dL]; 70/30: 8.6+/-1.9 mmol/L [154+/-34 mg/dL), analyses of the excursion parameters provide a truer comparison of the glucodynamic response between insulin formulations. Mix75/25 resulted in significantly lower values for 2pp(ex) (3.35+/-2.28 vs 4.13+/-2.26 mmol/L), Gex(max) (4.51+/-1.88 vs 5.19+/-1.98 mmol/L), and AUCex4 (8.01+/-7.02 vs 10.6+/-6.47 mmol x h/L) compared with 70/30.
In patients with type 2 diabetes mellitus, premeal injection of Mix75/25 resulted in better postprandial glycemic control than did premeal injection of 70/30 in the 4 hours after a standard meal. Mix75/25 is a valuable option for managing postprandial blood glucose in patients with type 2 diabetes mellitus who require insulin.
本双盲研究旨在比较一种新型预混胰岛素类似物Humalog Mix75/25(含75%中性精蛋白赖脯胰岛素和25%赖脯胰岛素)与人类胰岛素70/30(70%中性精蛋白锌胰岛素和30%普通人类胰岛素)在2型糖尿病患者中的餐后血糖动态变化情况。
赖脯胰岛素Mix75/25(Mix75/25)是首个速效和基础成分均为胰岛素类似物的胰岛素制剂。
本随机、多中心、双盲、交叉研究监测了患者在标准试验餐后对Mix75/25和人类胰岛素70/30(70/30)的餐后血糖动态反应。84例2型糖尿病患者参与了本研究,并被随机分配到2个治疗顺序组中的1组。患者在4个不同时间接受相同的试验餐,每种治疗完成2次试验餐。在2次试验餐每次餐前5分钟给予等量的Mix75/25或70/30,剂量根据每位患者个体化。餐后4小时采集血样以测定血浆葡萄糖。根据这些血浆葡萄糖测量值,计算空腹血浆葡萄糖、餐后2小时血糖(2pp)、餐后2小时血糖波动幅度(2pp(ex))、最大血糖波动幅度(Gex(max))、0至4小时葡萄糖浓度-时间曲线下面积(AUC4)以及0至4小时血糖波动-时间曲线下面积(AUCex4)。
由于Mix75/25和70/30之间基线空腹血浆葡萄糖水平存在显著差异(Mix75/25:8.9±2.2 mmol/L [160.2±39.6 mg/dL];70/30:8.6±1.9 mmol/L [154±]),对波动参数的分析能更真实地比较胰岛素制剂之间的血糖动态反应。与70/30相比,Mix75/25导致2pp(ex)(3.35±2.28对4.十三±2.26 mmol/L)、Gex(max)(4.51±1.88对5.19±1.98 mmol/L)和AUCex4(8.01±7.02对10.6±6.47 mmol·h/L)的值显著更低。
在2型糖尿病患者中,餐前注射Mix75/25在标准餐后4小时内比餐前注射70/30能更好地控制餐后血糖。Mix75/25是需要胰岛素治疗的2型糖尿病患者控制餐后血糖的一个有价值的选择。