Galic Eduard, Vrtovec Matjaz, Bozikov Velimir, Schwarzenhofer Maria, Milicevic Zvonko
Clinic for Internal Medicine, Department of Endocrinology and Diabetes, General Hospital Sveti Duh, Zagreb, Croatia.
Med Sci Monit. 2005 Dec;11(12):PI87-92. Epub 2005 Nov 24.
Postprandial hyperglycemia contributes to glycation of hemoglobin A1c and has been associated with cardiovascular risk in people with diabetes. We investigated the impact of injection timing of Humalog Mix25 (Mix25, known as Humalog Mix75/25 in the U.S.: 25% insulin lispro and 75% neutral protamine lispro) on glycemia and postprandial blood glucose (BG) excursions in elderly individuals
MATERIAL/METHODS: Seventy-three patients aged 60 to 80 years were randomized to Mix25 (Mix25 group, 37 participants) or a continuation with maximum dose glibenclamide (control group, 36 participants). The Mix25 group was subdivided into a group of 18 patients who were injecting insulin after meals and 19 who were injecting before.
At baseline, the absolute postprandial BG concentrations and postprandial BG excursions after breakfast were high (Mix25 group: 15.3+/-4.8 mmol/l and 3.5+/-2.7 mmol/l, respectively; controls: 15.4+/-3.9 mmol/l and 4.7+/-2.7 mmol/l, respectively). In both groups improvement was observed at the endpoint, but it was greater with Mix25 (Mix25 group: 10.3+/-3.6 mmol/l, p<0.0001 vs. baseline, p<0.003 vs. controls, and 2.0+/-2.5 mmol/l, p<0.008 vs. baseline, p=ns vs. controls; control group: 13.3+/-2.9 mmol/l, p<0.006 vs. baseline, and 4.7+/-2.7 mmol/l, p<0.006 vs. baseline). The two Mix25 subgroups had similar postprandial BG levels and BG excursions after breakfast.
Mix25 improves postprandial BG and yields a greater effect on BG excursions compared with monotherapy with glibenclamide. The timing of Mix25 did not impact the level of BG or BG fluctuations after meals, which may be important for individuals with changing dietary pattern.
餐后高血糖会导致糖化血红蛋白A1c升高,并与糖尿病患者的心血管风险相关。我们研究了优泌林75/25(在美国称为优泌乐75/25:25%赖脯胰岛素和75%精蛋白锌赖脯胰岛素)注射时间对老年个体血糖及餐后血糖(BG)波动的影响。
材料/方法:73例年龄在60至80岁的患者被随机分为优泌林75/25组(优泌林75/25组,37名参与者)或继续使用最大剂量格列本脲组(对照组,36名参与者)。优泌林75/25组又分为18例餐后注射胰岛素的患者和19例餐前注射胰岛素的患者。
基线时,早餐后绝对餐后BG浓度和餐后BG波动较高(优泌林75/25组:分别为15.3±4.8 mmol/l和3.5±2.7 mmol/l;对照组:分别为15.4±3.9 mmol/l和4.7±2.7 mmol/l)。两组在终点时均有改善,但优泌林75/25组改善更大(优泌林75/25组:10.3±3.6 mmol/l,与基线相比p<0.0001,与对照组相比p<0.003;2.0±2.5 mmol/l,与基线相比p<0.008,与对照组相比p=无显著性差异;对照组:13.3±2.9 mmol/l,与基线相比p<0.006;4.7±2.7 mmol/l,与基线相比p<0.006)。两个优泌林75/25亚组早餐后餐后BG水平和BG波动相似。
与格列本脲单药治疗相比,优泌林75/25可改善餐后BG,并对BG波动产生更大影响。优泌林75/2�的注射时间不影响餐后BG水平或BG波动,这对饮食模式多变的个体可能很重要。