DOI: 10.2337/dc07-1378
A Randomized Trial Comparing Continuous Subcutaneous Insulin Infusion of Insulin Aspart versus Insulin Lispro in Children and Adolescents with Type 1 Diabetes
1Yale University School of Medicine, New Haven, Connecticut stuart.weinzimer{at}yale.edu ABSTRACT Objective: The safety and efficacy of insulin aspart in continuous subcutaneous insulin infusion (CSII) was compared to that of insulin lispro CSII in children and adolescents with type 1 diabetes.
Research Design and Methods: Children and adolescents 4-18 years of age with diagnosed type 1 diabetes Results: Baseline demographics, subject characteristics, and diabetes history were similar between treatment groups. After 16 weeks of treatment, insulin aspart CSII was non-inferior to insulin lispro CSII as measured by change in HbA1c from baseline (aspart, –0.15±0.05%; lispro, –0.05±0.07%; 95% CI of the treatment difference, [-0.27, 0.07]; p=0.241). No significant differences between treatment groups were observed in fasting plasma glucose (FPG), hyperglycemia, and rates of hypoglycemic episodes. At Week 16, 59.7% of subjects in the aspart group and 43.8% of subjects in the lispro groups achieved age-specific ADA HbA1c goals (<8.5% for subjects < 6 years; <8% for subjects 6-18 years) (p=0.040, corrected for baseline). Daily insulin dose (U/kg) was significantly lower at Week 16 for subjects treated with aspart, as compared to those treated with lispro (0.86±0.237 vs. 0.94±0.233, p=0.018). Conclusions: Insulin aspart was as safe and effective as insulin lispro for use in CSII in children and adolescents with type 1 diabetes.
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