Volume 16, Issue 4 pp. 299-304
Original Article

Insulin glargine metabolite 21A-Gly-human insulin (M1) is the principal component circulating in the plasma of young children with type 1 diabetes: results from the PRESCHOOL study

Thomas Danne

Corresponding Author

Thomas Danne

“Auf der Bult” Children and Youth Hospital, Hannover, Germany

Corresponding author: Prof. Thomas Danne, MD,

“Auf der Bult” Children and Youth Hospital,

Diabetes Centre for Children and Adolescents,

Janusz-Korczak-Allee 12,

30173 Hannover,

Germany.

Tel: +49 511 8115 3330;

fax: +49 511 8115 5334;

e-mail: [email protected]

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Reinhard HA Becker

Reinhard HA Becker

Sanofi, Frankfurt, Germany

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Lin Ping

Lin Ping

Sanofi, Bridgewater, NJ, USA

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Areti Philotheou

Areti Philotheou

UCT Private Academic Hospital, Cape Town, South Africa

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First published: 09 July 2014
Citations: 7
This article was published online on July 09, 2014. An error was subsequently identified in table 2. This notice is included in the online and print versions to indicate that both have been corrected. [29 August 2014]

Abstract

Background and Aims

Insulin glargine metabolite 21A-Gly-human insulin (M1) is the principal component circulating in plasma of adults with type 1 diabetes. The objective of this study was to confirm this finding in young children and to rule out accumulation of parent insulin glargine.

Design and Methods

Children with type 1 diabetes from the PRESCHOOL study, aged 2–6 yr, were treated with insulin glargine for 24 wk (n = 62). Blood samples were drawn at weeks 1, 2, and 4 approximately 24 h after the last dose and analyzed for glargine, M1, and Thr30B-des-M1 (M2) using immunoaffinity purification and liquid chromatography with mass spectrometry. The lower limit of quantification was 33 pmol/L for all analytes.

Results

M1 was the principal active component circulating in plasma. Mean (SD) plasma Ctrough values were 101 (138), 80 (122), and 79 (102) pmol/L following glargine doses of 0.33 (0.02), 0.34 (0.02), and 0.38 (0.03) U/kg at weeks 1, 2, and 4, respectively. Parent insulin glargine and M2 concentrations were below the level of quantification. These results are in line with those observed in adults and indicate no accumulation of the parent compound in this patient population.

Conclusion

In young children with type 1 diabetes, the principal component circulating in plasma after subcutaneous injection of insulin glargine is M1, the pharmacologically active component. No accumulation of the parent insulin glargine was observed. These data provide additional evidence on the safety profile of insulin glargine in young children (Clinical trial identifier: NCT00993473).

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