胰岛素利斯普罗改善糖尿病患者餐后血糖控制。

Sbornik lekarsky Pub Date : 2002-01-01
J Skrha, A Smahelová, M Andĕl, M Vrtovec, J Subić, A Kreze, J Vozar, M Korecová, V de Verga, J Wyatt, S Metcalfe, S Ristić
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引用次数: 0

摘要

比较利斯普罗胰岛素与常规人胰岛素对强化胰岛素治疗的糖尿病患者血糖控制的影响。62例患者(1型55例;来自捷克共和国、斯洛文尼亚和斯洛伐克共和国八个研究中心的7例2型患者参加了为期4个月的开放标签、随机、交叉研究。患者在饭前立即使用胰岛素利斯普罗或在饭前30分钟使用常规人胰岛素。试验餐(220-400千卡),基于当地和个人饮食习惯,并在整个研究过程中为每个患者提供一致的基线和每次治疗结束时。在每次测试餐时,测量HbA1c、空腹血糖、餐后1小时和2小时血糖水平。HbA1c水平(7.6% +/- 1.5%对7.4% +/- 1.5%)、低血糖发生率(41-66%对39-63%)和每日胰岛素剂量(0.67 +/- 0.11 U/kg对0.65 +/- 0.11 U/kg)在治疗组之间无差异(分别为胰岛素lispro和常规人胰岛素)。与常规胰岛素组(1.3 +/- 3.7 mmol/L)相比,胰岛素lispro组餐后2小时平均血糖漂移(0.0 +/- 3.7 mmol/L)显著降低(p = 0.035)。因此,与常规人胰岛素相比,胰岛素利斯普罗治疗与餐后血糖漂移控制的显著改善相关,而低血糖发生率没有增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Insulin lispro improves postprandial glucose control in patients with diabetes mellitus.

Insulin lispro was compared with regular human insulin with respect to glycaemic control in patients with diabetes mellitus on intensive insulin treatment. Sixty-two patients (55 type 1; 7 type 2) from eight study centres in the Czech Republic, Slovenia and the Slovak Republic participated in a 4-month, open-label, randomized, crossover study. Patients administered insulin lispro immediately before meals or regular human insulin 30 min before meals. A test meal (220-400 kcal), based on local and individual dietary habits and consistent for each patient throughout the study was given at baseline and at the end of each treatment. At each test meal visit HbA1c, fasting blood glucose, 1-hour and 2-hour postprandial blood glucose levels were measured. The level of HbA1c (7.6% +/- 1.5% versus 7.4% +/- 1.5%), incidence of hypoglycaemia (41-66% of patients--versus 39-63%) and daily insulin dose (0.67 +/- 0.11 U/kg versus 0.65 +/- 0.11 U/kg) did not differ between treatment groups at endpoint (insulin lispro versus regular human insulin, respectively). Mean 2-hour postprandial blood glucose excursion for the insulin lispro group (0.0 +/- 3.7 mmol/L) was significantly lower (p = 0.035) when compared with the regular human insulin group (1.3 +/- 3.7 mmol/L) at endpoint. Therapy with insulin lispro was therefore associated with a significant improvement in postprandial blood glucose excursion control when compared with regular human insulin, without an increase in rate of hypoglycaemia.

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