Cited by 153Diabetes Management and ResearchDiabetes Treatment and ManagementDiabetes and associated disorders

Insulin Detemir Is Characterized by a Consistent Pharmacokinetic Profile Across Age-Groups in Children, Adolescents, and Adults With Type 1 Diabetes

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Danne, Thomas, Lüpke, Kerstin, Walte, Kerstin, von Schuetz, Wolfgang, Gall, Mari-Anne·2003·Diabetes Care

Abstract

OBJECTIVE—This trial aimed to characterize for the first time the pharmacokinetic profile of insulin detemir, the novel soluble basal insulin analog, in children and adolescents compared with adults. Comparisons were also made with NPH insulin to determine any between-treatment difference in the effect of age on pharmacokinetic profile. RESEARCH DESIGN AND METHODS—This single-center, open-label, randomized, crossover trial included children (aged 6–12 years, n = 13), adolescents (aged 13–17 years, n = 10), and adults (aged 18–65 years, n = 11) of both sexes. Subjects were given single doses of 0.5 units/kg s.c. insulin detemir or 0.5 IU/kg NPH insulin on 2 separate days. Serial blood sampling was performed for 24 h for analysis of serum insulin detemir, human insulin, and glucose concentrations. RESULTS—The mean pharmacokinetic profile of insulin detemir was similar across all three age-groups. This was determined by statistical analyses of the data, which showed no overall age effect or between-group differences when pairwise comparisons were made between children (or adolescents) and adults on the parameters of the area under the curve (AUC), AUC from zero to infinity, AUC from 0 to 24 h [AUC(0–24 h)], and the maximum concentration measured during the 24 h after closing. No overall age effect for AUC(0–24 h) and Cmax was detected for NPH insulin, but data were only analyzable from seven adults and pairwise comparisons did indicate that children and adults had different pharmacokinetic profiles. Less total variability in the pharmacokinetics of insulin detemir than NPH insulin was indicated by lower coefficients of variation in AUC, Cmax, and time to maximum concentration in all three age-groups. CONCLUSIONS—The data suggest that insulin detemir can be used in children and adolescents with type 1 diabetes using titration guidelines similar to those used in adults. Moreover, insulin detemir may offer the advantage of greater predictability of response in comparison to NPH insulin due to lower total variability and a lesser degree of kinetic disparity across age-groups.

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Crossref · 10.2337/diacare.26.11.3087

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  • Previous investigations with another basal analogue have shown that pharmacological exposure can be higher in children and adolescents than in adults.

    “Previous investigations with another basal analogue have shown that the pharmacological exposure can be higher in children and adolescents than in adults [39].”

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Authors
Danne, T., Lüpke, K., Walte, K., von Schuetz, W., & Gall, M.-A.
Affiliations
  • Kinderkrankenhaus auf der Bult (DE)
  • Kinderkrankenhaus auf der Bult, Hannover, Germany
  • Novo Nordisk (Denmark) (DK)
Venue
Diabetes Care
Published
2003-11-01
Volume
26
Issue
11
Pages
3087-3092
ISSN
  • 0149-5992 (ISSN-L)
  • 1935-5548
OpenAlex
W2063822715
Cited by
153
References
4
Citations by year
2026: 2 · 2025: 5 · 2024: 1 · 2023: 1 · 2022: 6 · 2021: 5 · 2020: 5 · 2019: 5 · 2018: 4 · 2017: 3 · 2015: 4 · 2014: 12 · 2013: 3 · 2012: 5
FWCI
6.10
Type
journal article
Language
en
Open access
Locations
  • Diabetes Care (publishedVersion)
  • PubMed (publishedVersion)
Funders
Novo Nordisk
Topics
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Management and Research
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Treatment and Management
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Diabetes and associated disorders
Keywords
insulin detemir, pharmacokinetics, type 1 diabetes, age differences, children and adolescents, NPH insulin, basal insulin analogues, insulin dose, pharmacokinetic variability, insulin dose adjustment
MeSH terms
Insulin Detemir, Adolescent, Adult, Age Factors, Aged, Carrier Proteins, Child, Diabetes Mellitus, Type 1, Female, Humans, Hypoglycemic Agents, Insulin, Insulin, Isophane, Male, Middle Aged, Cross-Over Studies, Insulin, Long-Acting

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