药理学
门冬氨酸胰岛素
胰岛素类似物
加药
曲线下面积
耐受性
作者
Johannes Plank,Manfred Bodenlenz,Frank Sinner,Christoph Magnes,Evelyn Görzer,Werner Regittnig,Lars Endahl,Eberhard Draeger,Milan Zdravkovic,Thomas R. Pieber
出处
期刊:Diabetes Care
[American Diabetes Association]
日期:2005-05-01
卷期号:28 (5): 1107-1112
被引量:251
标识
DOI:10.2337/diacare.28.5.1107
摘要
Objective To investigate the pharmacodynamic profile and duration of action for five subcutaneous doses of insulin detemir (0.1, 0.2, 0.4, 0.8, and 1.6 units/kg; 1 unit = 24 nmol) and one subcutaneous dose of NPH insulin (0.3 IU/kg; 1 IU = 6 nmol). Research design and methods This single-center, randomized, double-blind, six-period, crossover study was carried out as a 24-h isoglycemic clamp (7.2 mmol/l) in 12 type 1 diabetic patients. Results Duration of action for insulin detemir was dose dependent and varied from 5.7, to 12.1, to 19.9, to 22.7, to 23.2 h for 0.1, 0.2, 0.4, 0.8, and 1.6 units/kg, respectively. Interpolation of the dose-response relationships for AUC(GIR) (area under the glucose infusion rate curve) revealed that a detemir dose of 0.29 units/kg would provide the same effect as 0.3 IU/kg NPH but has a longer duration of action (16.9 vs. 12.7 h, respectively). Lower between-subject variability was observed for insulin detemir on duration of action (0.4 units/kg insulin detemir vs. 0.3 IU/kg NPH, P Conclusions This study shows that insulin detemir provides a flat and protracted pharmacodynamic profile.
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