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Diabetes Care Publish Ahead of Print published online ahead of print November 5, 2007
DOI: 10.2337/dc07-1378

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Original Research

A Randomized Trial Comparing Continuous Subcutaneous Insulin Infusion of Insulin Aspart versus Insulin Lispro in Children and Adolescents with Type 1 Diabetes

Stuart A. Weinzimer, MD1, Christine Ternand, MD2, Campbell Howard, MD3, Cheng-Tao Chang, PhD3, Dorothy J. Becker, MB, BCh4, Lori M.B. Laffel, MD, MPH For the Insulin Aspart Pediatric Pump Study Group5

1Yale University School of Medicine, New Haven, Connecticut
2University of Minnesota Physicians, Minneapolis, Minnesota
3Novo Nordisk Inc., Princeton, New Jersey
4Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania
5Joslin Diabetes Center, Boston, Massachusetts

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 ≥1 year previously treated with insulin analog CSII ≥3 months were randomized 2:1 to 16 weeks of insulin aspart CSII (n=198) or insulin lispro CSII (n=100) in this open-label, parallel-group, multicenter study. Standard diabetes safety and efficacy parameters were assessed.

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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