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 2026-05-28A 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.
| Journal | J Pediatr Endocrinol Metab, 2015 |
|---|---|
| Citations | 12 |
| Relative citation ratio | 0.50 |
| NIH percentile | 29 |
| 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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