Adolescents with obesity treated with exenatide maintain endogenous GLP-1, reduce DPP-4, and improve glycemic control

Front Endocrinol (Lausanne). 2023 Nov 1:14:1293093. doi: 10.3389/fendo.2023.1293093. eCollection 2023.

Abstract

Background: GLP-1 receptor agonists (GLP-1RA) are increasingly used to treat adolescent obesity. However, the effect on endogenous GLP-1 secretory patterns following treatment in adolescents is unknown. The GLP-1RA exenatide was shown to significantly lower BMI and 2-hour glucose in adolescents with obesity, in the placebo-controlled, randomized controlled trial Combat-JUDO. The aim of this study was to evaluate effects of weekly injections of 2 mg exenatide extended release on secretory patterns of endogenous hormones during OGTT.

Subjects and measurements: This study was a pre-planned sub-study of the Combat-JUDO trial, set at the Pediatric clinic at Uppsala University Hospital, Sweden and Paracelsus Medical University, Austria. 44 adolescents with obesity were included and randomized 1:1 to treatment:placebo. 19 patients in the treatment group and 18 in the placebo group completed the trial. Before and after treatment, GLP-1, glucose, insulin, glucagon and glicentin levels were measured during OGTT; DPP-4 and proinsulin were measured at fasting. A per-protocol approach was used in the analyses.

Results: Exenatide treatment did not affect GLP-1 levels during OGTT. Treatment significantly lowered DPP-4, proinsulin and the proinsulin-to-insulin ratio at fasting, increased glicentin levels but did not affect insulin, C-peptide or glucagon levels during OGTT.

Conclusion: Weekly s.c. injections with 2 mg of exenatide maintains endogenous total GLP-1 levels and lowers circulating DPP-4 levels. This adds an argument in favor of using exenatide in the treatment of pediatric obesity.

Clinical trial registration: clinicaltrials.gov, identifier NCT02794402.

Keywords: obesity; GLP-1; GLP-1 receptor agonist; GLP-1 receptor analog; exenatide; glycemic control; pediatrics; treatment.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Child
  • Exenatide
  • Glicentin
  • Glucagon
  • Glucagon-Like Peptide 1*
  • Glucose
  • Glycemic Control
  • Humans
  • Insulin
  • Pediatric Obesity* / drug therapy
  • Proinsulin

Substances

  • Exenatide
  • Glucagon-Like Peptide 1
  • Glucagon
  • Proinsulin
  • Glicentin
  • Insulin
  • Glucose

Associated data

  • ClinicalTrials.gov/NCT02794402

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. Support from the European the Union Seventh Framework Programme (FP7/2007-2013) under grant agreement number 279153 (Beta-JUDO), the Regional Research Council in Uppsala-Örebro, Sweden, the Swedish Diabetes Foundation, the Swedish Society for Diabetology, the Gillbergska Foundation, Swedish Research Council (2016-01040), and AstraZeneca was received for the study.