Authors
Daniel C Howey, Ronald R Bowsher, Rocco L Brunelle, Howard M Rowe, Paula F Santa, Joyce Downing‐Shelton, James R Woodworth
Publication date
1995/10
Journal
Clinical Pharmacology & Therapeutics
Volume
58
Issue
4
Pages
459-469
Description
Background
[Lys(B28), Pro(B29)]‐human insulin (lispro) is an insulin analogue with a reduced capacity for self‐association and faster absorption from subcutaneous injection sites. We hypothesized that administration of lispro closer to a meal would result in better glucose control than that achieved with regular insulin.
Methods
This trial used a randomized crossover design that consisted of a period of metabolic stabilization lasting 9 days followed by an evaluation period lasting 5 days. The patients received weight‐maintenance diets, and insulin doses were adjusted as needed. Calorie intake, insulin dose, and activities were kept constant once the evaluation period began. During the evaluation period, we varied the time between insulin injection and mealtime and assessed glucose control.
Results
During the evaluation period, the lowest mean glucose concentrations were 117.9 mg/dl for lispro and 119.8 mg …
Total citations
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Scholar articles
DC Howey, RR Bowsher, RL Brunelle, HM Rowe… - Clinical Pharmacology & Therapeutics, 1995