Malone J K, Bai S, Campaigne B N, Reviriego J, Augendre-Ferrante B
Lilly Research Laboratories, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA.
Diabet Med. 2005 Apr;22(4):374-81. doi: 10.1111/j.1464-5491.2005.01511.x.
To compare the glycaemic control of an insulin lispro mixture (25% insulin lispro and 75% NPL) twice daily in combination with metformin to that of once-daily insulin glargine plus metformin in patients with Type 2 diabetes inadequately controlled with intermediate insulin, or insulin plus oral agent(s) combination therapy.
Ninety-seven patients were randomized in a multicentre, open-label, 32-week crossover study. Primary variables evaluated: haemoglobin A1c (A1c), 2-h post-prandial blood glucose (BG), hypoglycaemia rate (episodes/patient/30 days), incidence (% patients experiencing > or = 1 episode) of overall and nocturnal hypoglycaemia.
At endpoint, A1c was lower with the insulin lispro mixture plus metformin compared with glargine plus metformin (7.54% +/- 0.87% vs. 8.14% +/- 1.03%, P < 0.001). Change in A1c from baseline to endpoint was greater with the insulin lispro mixture plus metformin (-1.00% vs. -0.42%; P < 0.001). Two-hour post-prandial BG was lower after morning, midday, and evening meals (P < 0.001) during treatment with the insulin lispro mixture plus metformin. The fasting BG values were lower with glargine plus metformin (P = 0.007). Despite lower BG at 03.00 hours (P < 0.01), patients treated with the insulin lispro mixture plus metformin had a lower rate of nocturnal hypoglycaemia (0.14 +/- 0.49 vs. 0.34 +/- 0.85 episodes/patient/30 days; P = 0.002), although the overall hypoglycaemia rate was not different between treatments (0.61 +/- 1.41 vs. 0.44 +/- 1.07 episodes/patient/30 days; P = 0.477).
In patients with Type 2 diabetes and inadequate glucose control while on insulin or insulin and oral agent(s) combination therapy, treatment with a twice-daily insulin lispro mixture plus metformin, which targets both post-prandial and pre-meal BG, provided clinically significant improvements in A1c, significantly reduced post-prandial BG after each meal, and reduced nocturnal hypoglycaemia as compared with once-daily glargine plus metformin, a treatment that targets fasting BG.
比较每日两次注射赖脯胰岛素混合制剂(25%赖脯胰岛素和75%NPL)联合二甲双胍与每日一次注射甘精胰岛素联合二甲双胍,在接受中效胰岛素或胰岛素加口服降糖药联合治疗血糖控制不佳的2型糖尿病患者中的血糖控制情况。
97例患者参与了一项多中心、开放标签、为期32周的交叉研究并被随机分组。评估的主要变量包括:糖化血红蛋白(A1c)、餐后2小时血糖(BG)、低血糖发生率(事件数/患者/30天)、总体及夜间低血糖的发生率(经历≥1次低血糖事件的患者百分比)。
在研究终点,与甘精胰岛素联合二甲双胍相比,赖脯胰岛素混合制剂联合二甲双胍组的A1c更低(7.54%±0.87% vs. 8.14%±1.03%,P<0.001)。从基线到终点,赖脯胰岛素混合制剂联合二甲双胍组A1c的变化更大(-1.00% vs. -0.42%;P<0.001)。在用赖脯胰岛素混合制剂联合二甲双胍治疗期间,早餐、午餐和晚餐后2小时的BG更低(P<0.001)。甘精胰岛素联合二甲双胍组的空腹BG值更低(P = 0.007)。尽管在凌晨3点时BG较低(P<0.01),但赖脯胰岛素混合制剂联合二甲双胍治疗的患者夜间低血糖发生率更低(0.14±0.49 vs. 0.34±0.85事件数/患者/30天;P = 0.002),尽管两种治疗的总体低血糖发生率并无差异(0.61±1.41 vs. 0.44±1.07事件数/患者/30天;P = 0.477)。
在接受胰岛素或胰岛素与口服降糖药联合治疗但血糖控制不佳的2型糖尿病患者中,每日两次注射赖脯胰岛素混合制剂联合二甲双胍,这种针对餐后和餐前BG的治疗方案,与每日一次注射甘精胰岛素联合二甲双胍(一种针对空腹BG的治疗方案)相比,在A1c方面有显著临床改善,显著降低每餐餐后BG,并减少夜间低血糖。