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Three years of liraglutide treatment offers continuously optimal glycemic control in a pediatric patient with maturity-onset diabetes of the young type 3.

J Pediatr Endocrinol Metab · 2015

Last updated 2026-05-28

A 12-year-old girl with a rare form of diabetes (MODY3) switched from insulin to the GLP-1 drug liraglutide. Over 3 years, her blood sugar control stayed stable with hemoglobin A1c levels between 6.8% and 7.5%, and her body’s insulin production remained above 3.0 ng/mL. No side effects from liraglutide were reported during this time.

AI summary of the abstract below.

JournalJ Pediatr Endocrinol Metab, 2015
Citations12
Relative citation ratio0.50
NIH percentile29
Molecules liraglutide
Conditions studied Type 2 Diabetes

Abstract

Sulfonylureas (SUs) are recommended as the first-line pharmacological treatment in patients with uncontrolled maturity-onset diabetes of the young type 3 (MODY3). In contrast, glucagon-like peptide-1 (GLP-1) receptor agonists have the advantages of a low risk of hypoglycemia and maintained β-cell function. We report a pediatric patient with MODY3 treated with a GLP-1 receptor agonist, liraglutide. A 12-year-old Japanese girl with MODY3 had been treated with insulin for 6 months since the time of diagnosis. After genetic analysis, we switched her treatment from insulin to liraglutide. After switching to liraglutide, the patient maintained optimal glycemic control with hemoglobin A₁c levels of 6.8%-7.5% and had postprandial C-peptide levels >3.0 ng/mL during a 3-year treatment period. No adverse events associated with liraglutide were observed. GLP-1 receptor agonists are the potential medications for patients with MODY3 who maintain residual insulin secretion.

Verbatim abstract via PubMed 25332292 ↗

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