- Liraglutide and semaglutide produce clinically meaningful weight loss in adolescents, leading to FDA and EMA approvals for patients aged 12 years and older.
- Common adverse events are gastrointestinal, with no consistent effects on growth or puberty reported, but long term safety and outcome data remain limited.
- Pharmacotherapy should complement intensive lifestyle and family based interventions, address psychosocial risks and access disparities, and may combine with surgery or other agents.
Dig Liver Dis. 2026 Jul 4:S1590-8658(26)00776-0. doi: 10.1016/j.dld.2026.06.010. Online ahead of print.
ABSTRACT
Glucagon-like peptide-1 receptor agonists (GLP-1RAs) have transformed the management of obesity in adults and are now gaining attention in pediatric populations facing a dramatic rise of obesity prevalence and related comorbidities. In addition to weight loss, their role extends to cardiometabolic effects and improvements of kidney function. Liraglutide and semaglutide have demonstrated clinically meaningful efficacy in adolescents, leading to FDA and EMA approvals for patients ≥12 years. Ongoing trials are being conducted to combine GLP-1 analogues with other effective molecules or with bariatric surgery. Current evidence on safety most frequently highlights gastrointestinal adverse events, with no consistent impact on growth or pubertal development reported to date. Psychosocial dimensions, including stigma, mental health risks, and potential disordered eating, together with economic barriers and disparities in access, require careful consideration and efforts to be overcome. Implementing intensive lifestyle interventions is mandatory, including nutritional education, physical activity promotion, and family-based behavioral strategies, to support long-term weight management and address the broader determinants of health. Preliminary studies suggest complementary roles for GLP-1RAs alongside metabolic bariatric surgery in selected high-risk patients. Long-term data on safety and multidisciplinary approaches are required to define the optimal integration of pharmacotherapy into comprehensive, family-centered pediatric obesity care models.
PMID:42401514 | DOI:10.1016/j.dld.2026.06.010
Share Evidence Blueprint

Search Google Scholar
Save as PDF

