A 6-month randomized, double-blind, placebo-controlled trial of weekly exenatide in adolescents with obesity.
Pediatr Obes · 2020
Last updated 2026-05-28In a 6-month study of 44 adolescents with obesity, those given weekly injections of exenatide (2 mg) alongside lifestyle changes saw small but notable improvements compared to those given a placebo. Exenatide users had a slight reduction in BMI (-0.09), weight (-3 kg), waist size (-3.2 cm), and better blood sugar control during glucose tests (-15.3 mg/dL), as well as lower total cholesterol (-11.6 mg/dL). Mild side effects were more common with exenatide, but serious issues were similar to the placebo group.
AI summary of the abstract below.
| Journal | Pediatr Obes, 2020 |
|---|---|
| Citations | 57 |
| Relative citation ratio | 3.11 |
| NIH percentile | 85 |
| Molecules | exenatide |
| Conditions studied | Obesity |
Abstract
BACKGROUND: Pharmacological treatment options for adolescents with obesity are very limited. Glucagon-like-peptide-1 (GLP-1) receptor agonist could be a treatment option for adolescent obesity.
OBJECTIVE: To investigate the effect of exenatide extended release on body mass index (BMI)-SDS as primary outcome, and glucose metabolism, cardiometabolic risk factors, liver steatosis, and other BMI metrics as secondary outcomes, and its safety and tolerability in adolescents with obesity.
METHODS: Six-month, randomized, double-blinded, parallel, placebo-controlled clinical trial in patients (n = 44, 10-18 years, females n = 22) with BMI-SDS > 2.0 or age-adapted-BMI > 30 kg/m according to WHO were included. Patients received lifestyle intervention and were randomized to exenatide extended release 2 mg (n = 22) or placebo (n = 22) subcutaneous injections given once weekly. Oral glucose tolerance tests (OGTT) were conducted at the beginning and end of the intervention.
RESULTS: Exenatide reduced (P < .05) BMI-SDS (-0.09; -0.18, 0.00), % BMI 95th percentile (-2.9%; -5.4, -0.3), weight (-3 kg; -5.8, -0.1), waist circumference (-3.2 cm; -5.8, -0.7), subcutaneous adipose tissue (-552 cm ; -989, -114), 2-hour-glucose during OGTT (-15.3 mg/dL; -27.5, -3.1), total cholesterol (11.6 mg/dL; -21.7, -1.5), and BMI (-0.83 kg/m ; -1.68, 0.01) without significant change in liver fat content (-1.36; -3.12, 0.4; P = .06) in comparison to placebo. Safety and tolerability profiles were comparable to placebo with the exception of mild adverse events being more frequent in exenatide-treated patients.
CONCLUSIONS: Treatment of adolescents with severe obesity with extended-release exenatide is generally well tolerated and leads to a modest reduction in BMI metrics and improvement in glucose tolerance and cholesterol. The study indicates that the treatment provides additional beneficial effects beyond BMI reduction for the patient group.
Verbatim abstract via PubMed 32062862 ↗
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