The effect of glucagon-like peptide-1 receptor agonist therapy on body mass index in adolescents with severe obesity: a randomized, placebo-controlled, clinical trial.
JAMA Pediatr · 2013
Last updated 2026-05-28In a small 3-month study of 26 teens with severe obesity, those who took the GLP-1 drug exenatide (along with lifestyle counseling) lost more weight than those who took a placebo—about 3.3 kg (7.3 lbs) more on average. Their BMI dropped by 2.7% compared to the placebo group. Blood pressure also improved slightly, though not enough to be considered statistically significant. After another 3 months of open-label treatment, teens who continued exenatide saw their BMI drop by a total of 4%.
AI summary of the abstract below.
| Journal | JAMA Pediatr, 2013 |
|---|---|
| Citations | 141 |
| Relative citation ratio | 4.96 |
| NIH percentile | 92 |
| Molecules | — |
| Conditions studied | Obesity |
Abstract
IMPORTANCE: Medical treatment options for pediatric obesity remain limited. Glucagon-like peptide-1 (GLP-1) receptor agonists induce weight loss by suppressing appetite and increasing satiety, but few studies have evaluated this therapy as a treatment for obesity.
OBJECTIVE: To evaluate the effects of exenatide on body mass index (BMI; calculated as weight in kilograms divided by height in meters squared) and cardiometabolic risk factors in adolescents with severe obesity.
DESIGN: Three-month, randomized, double-blind, placebo-controlled, multicenter clinical trial followed by a 3-month open-label extension.
SETTING: An academic medical center and an outpatient pediatric endocrinology clinic.
PATIENTS: A total of 26 adolescents (12-19 years of age) with severe obesity (BMI ≥ 1.2 times the 95th percentile or BMI ≥ 35).
INTERVENTION: All patients received lifestyle modification counseling and were equally randomized to exenatide or placebo injection, twice per day.
MAIN OUTCOME MEASURES: The primary end point was the mean percent change in BMI measured at baseline and 3 months. Secondary end points included absolute change in BMI, body weight, body fat, blood pressure, hemoglobin A1c, fasting glucose, fasting insulin, and lipids at 3 months.
RESULTS: Twenty-two patients completed the trial. Exenatide elicited a greater reduction in percent change in BMI compared with placebo (-2.70% [95% CI, -5.02% to -0.37%]; P = .03). Similar findings were observed for absolute change in BMI (-1.13 [95% CI, -2.03 to -0.24]; P = .02) and body weight (-3.26 kg [95% CI, -5.87 to -0.66 kg]; P = .02). Although not reaching the level of statistical significance, reduction in systolic blood pressure was observed with exenatide. During the open-label extension, BMI was further reduced in those initially randomized to exenatide (cumulative BMI reduction of 4%).
CONCLUSIONS AND RELEVANCE: These results provide preliminary evidence supporting the feasibility, safety, and efficacy of GLP-1 receptor agonist therapy for the treatment of severe obesity in adolescents.
TRIAL REGISTRATION: clinicaltrials.gov Identifier: NCT01237197.
Verbatim abstract via PubMed 23380890 ↗