Ahmed A B, Mallias J, Home P D
Human Metabolism and Diabetes Research Centre, University of Newcastle-upon-Tyne, U.K.
Diabetes Care. 1998 Jul;21(7):1162-6. doi: 10.2337/diacare.21.7.1162.
A three-way, crossover, open-label, randomized study was designed to compare the evening and night (1800-0800) glycemic control when the evening premeal lispro dose was reduced by 20% and the bedtime basal NPH dose increased by 25%, or when the basal NPH dose was moved to before dinner at 1800, compared with the control arm on standard premeal human regular insulin and pre-bedtime NPH insulin.
A total of 13 type 1 diabetic patients who use a premeal plus basal insulin regimen were studied on three separate days, with identical meals and snacks at the same times on each study day. On the control study day, patients received human regular insulin before dinner and NPH at bedtime in their usual doses. On another day, lispro was given before dinner with a dose reduction of 20%, and NPH at bedtime at 125% of usual dose. In the third regimen, the lispro and NPH were administered together in their usual dose before the evening meal by separate injections. The three regimens were tested in random order.
Postprandial (1800-2200) blood glucose concentrations were lower after reduced-dose lispro compared with human regular insulin (6.0 +/- 0.3 [SEM] vs. 7.4 +/- 0.3 mmol/l, P < 0.05). Nighttime (2400-0400) blood glucose concentrations were not different (8.6 +/- 0.3 vs. 9.2 +/- 0.3 mmol/l, NS), and prebreakfast concentrations were also unchanged (7.7 +/- 0.9 vs. 8.7 +/- 0.8 mmol/l) after lispro with increased-dose NPH compared with standard insulin. By contrast, both nighttime (10.0 +/- 0.3 mmol/l, P < 0.05) and fasting glucose concentrations (10.8 +/- 0.6 mmol/l, P < 0.05) were significantly higher with dinnertime usual-dose lispro plus dinnertime usual-dose NPH compared with standard human insulin. Hypoglycemia at night (blood glucose < 3.0 mmol/l) did not differ between study days, but it was more frequent postprandially after dinner usual-dose lispro plus early NPH (2 vs. 7 patients, P = 0.062).
With lower mealtime and higher basal bedtime insulin doses, patients using insulin lispro may be able to gain an overall improvement in evening blood glucose control without deteriorated nighttime glucose levels. Earlier basal NPH dosage alone does not ameliorate the nighttime hyperglycemia of short-acting insulin analog regimens.
设计一项三臂、交叉、开放标签的随机研究,以比较当晚餐前赖脯胰岛素剂量减少20%且睡前中效胰岛素(NPH)剂量增加25%时,以及当将基础NPH剂量移至18:00晚餐前时,与使用标准餐前人常规胰岛素和睡前NPH胰岛素的对照组相比,傍晚和夜间(18:00至08:00)的血糖控制情况。
共13例使用餐时加基础胰岛素方案的1型糖尿病患者在三个不同日期接受研究,每个研究日的相同时间提供相同的餐食和零食。在对照研究日,患者按常规剂量在晚餐前接受人常规胰岛素,睡前接受NPH。在另一天,晚餐前给予赖脯胰岛素,剂量减少20%,睡前给予NPH,剂量为常规剂量的125%。在第三种方案中,赖脯胰岛素和NPH在晚餐前按常规剂量分别注射。三种方案按随机顺序进行测试。
与使用人常规胰岛素相比,减少剂量的赖脯胰岛素治疗后餐后(18:00至22:00)血糖浓度较低(6.0±0.3[标准误]对7.4±0.3 mmol/L,P<0.05)。与标准胰岛素相比,增加剂量NPH的赖脯胰岛素治疗后夜间(24:00至04:00)血糖浓度无差异(8.6±0.3对9.2±0.3 mmol/L,无统计学意义),早餐前血糖浓度也未改变(7.7±0.9对8.