Glucagon-like peptide-1 receptor agonists (GLP-1s) significantly improved glycemic, weight, and cardiometabolic outcomes in children and adolescents with type 2 diabetes (T2D) or obesity, according to data from a systemic review and meta-analysis of 18 trials published in JAMA Pediatrics. Study authors noted that further data over a short follow-up revealed that suicidal ideations or behavior did not demonstrate a significant difference; however, long-term gastrointestinal adverse effects need further research.1,2
Overview and Treatment Options for Childhood Obesity
Childhood obesity currently affects 1 in 5 children and adolescents younger than 18 years, rising from previous years along with a steady increase in T2D cases. In the past, treatment for T2D in children was limited to metformin and insulin, but in 2019 the FDA has approved various GLP-1s for this patient population, including liraglutide (Victoza; Novo Nordisk), semaglutide (Ozempic, Wegovy; Novo Nordisk), dulaglutide (Trulicity; Eli Lilly and Company), and extended-release exenatide (Bydureon BCise; Amylin Pharmaceuticals).
Approval of these medications along with updated pediatric guidelines has led to a significant increase in the use of GLP-1s for T2D and obesity in children and adolescents between 2020 and 2023. Additionally, tirzepatide, a dual-action medication, is currently being investigated for use in the same population.1
With the rising use of GLP-1s among youth, their psychological impacts are a concern, as suicide rates have grown, with 17% of US youth reporting suicidal ideation and 7% to 8% attempting suicide annually.1,2
Safety and Efficacy of GLP-1s in Children and Adolescents
To assess the efficacy and safety of GLP-1s in children and adolescents under 18 years with obesity, prediabetes, or T2D, researchers analyzed data from a total of 18 randomized clinical trials that were found through a systemic search in PubMed, Embase, and the Cochrane Central Register of Controlled Trials (CENTRAL).1,2
The efficacy of treatments was measured by several factors, including changes in hemoglobin A1c (HbA1c), fasting plasma glucose (FPG), and weight outcomes, including body weight, body mass index (BMI), and BMI scores. Blood pressure and lipid profiles were also assessed. The study authors also assessed exploratory outcomes that evaluated metabolic dysfunction-associated steatohepatitis (MASH), metabolic dysfunction-associated steatotic liver disease (MASLD), and obstructive sleep apnea (OSA).1,2
To evaluate safety, the trials assessed suicidal ideation and behaviors using the Columbia-Suicide Severity Rating Scale (C-SSRS), which groups these into 3 categories: suicidal ideation, suicidal behavior, and self-injury without intent. However, the study authors noted that in this analysis the 3 categories were combined into a single group referred to as suicidal ideation or behaviors. Researchers also assessed the safety of gastrointestinal adverse effects, infections, hepatobiliary disorders, hypoglycemia, and adverse event discontinuations.1,2
The results demonstrated that GLP-1s significantly reduced HbA1c by 44% and fasting glucose by 9.92 mg/dL. Patients also showed improved weight-related outcomes, decreasing body weight by 3.02 kg and BMI by 1.45, along with a decrease in systolic blood pressure.1,2
Further results demonstrated that the most common adverse effects were gastrointestinal, which were more frequent in participants using GLP-1s. However, the study found no significant differences in other adverse events, including suicidal ideation or behaviors between the GLP-1 and placebo groups.1,2
“To build on these findings, future clinical trials and real-world studies could assess treatment adherence with respect to patient preferences and their effect on safety and efficacy/effectiveness outcomes. Moreover, longer follow-up from future RCTs and real-world studies is essential to establish the long-term effects of GLP-1 RAs in children and adolescents,” the authors said in the study.1