# Glucagon-like peptide-1 agonists in children with obesity and type 2 diabetes. an umbrella review

**Authors:** Hyder Mirghani, Laila Albishi, Sawsan Mohmmad Alblewi

PMC · DOI: 10.3389/fendo.2026.1777907 · Frontiers in Endocrinology · 2026-02-19

## TL;DR

GLP-1 agonists help reduce weight and improve blood sugar in children with obesity or type 2 diabetes, with few side effects.

## Contribution

This umbrella review evaluates the effectiveness and safety of GLP-1 agonists in pediatric obesity and type 2 diabetes.

## Key findings

- GLP-1 agonists significantly reduced body weight, HbA1c, BMI z, and systolic blood pressure in children.
- Adverse events and hypoglycemia were comparable to controls, indicating good tolerability.
- Only 11 meta-analyses were included due to limited literature on this topic in pediatric populations.

## Abstract

Obesity and type 2 diabetes mellitus (Type 2 DM) are rising at an alarming rate among children and adolescents. This population often exhibits suboptimal glycemic control and diabetes-related complications. Glucagon-like peptide-1 receptor agonists (GLP-1 agonists) have emerged as a promising therapeutic option for pediatric patients due to their beneficial effects on weight reduction and glycemic regulation. Literature on this important issue is scarce. We aimed to assess the effects of GLP-1 agonists on body weight, HbA1c, body mass index z (BMI z), and systolic blood pressure (SBP). Additionally, we discussed adverse events and hypoglycemia.

We searched PubMed/MEDLINE, Web of Science, and the Cochrane Library from October to November 2025 using the following terms: GLP-1 agonists, semaglutide, tirzepatide, liraglutide, exenatide, children, obesity, adolescents, blood pressure, BMI z, hypoglycemia, body weight, and HbA1c. We retrieved 1600 articles. Out of the 44 reviews found, only 11 meta-analyses were included in the final results.

GLP-1 agonists were more effective than control in reducing body weight, HbA1c, BMI z, and blood pressure, MD = 0.11, 95% CI 0.05–0.25, MD = 0.65, 95% CI 0.53–0.80, MD = 0.85, 95% CI 0.81–0.90, and MD = 0.19, 95% CI 0.04–83, respectively. The total adverse events and hypoglycemia were not different, log ratios=1.29, 95% CI 0.80–2.09, and log ratios=1.26, 95% CI 0.59–2.70, respectively.

GLP-1 agonists are a promising and effective therapy for lowering weight, HbA1c, BMI z, and SBP in adolescents with obesity or youth with type 2 DM. Moreover, GLP-1 agonists were well tolerated, and the total adverse events and hypoglycemia were comparable to those of controls.

## Linked entities

- **Chemicals:** semaglutide (PubChem CID 56843331), tirzepatide (PubChem CID 163285897), liraglutide (PubChem CID 16134956), exenatide (PubChem CID 45588096)
- **Diseases:** obesity (MONDO:0011122), type 2 diabetes mellitus (MONDO:0005148)

## Full-text entities

- **Genes:** PPARG (peroxisome proliferator activated receptor gamma) [NCBI Gene 5468] {aka CIMT1, FPLD3, GLM1, NR1C3, PPARG1, PPARG2}, TCF7L2 (transcription factor 7 like 2) [NCBI Gene 6934] {aka TCF-4, TCF4}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, GLP1R (glucagon like peptide 1 receptor) [NCBI Gene 2740] {aka GLP-1, GLP-1-R, GLP-1R}, GCG (glucagon) [NCBI Gene 2641] {aka GLP-1, GLP1, GLP2, GRPP}
- **Diseases:** systolic reduction of blood pressure (MESH:D007022), depression (MESH:D003866), Obesity (MESH:D009765), type 2 diabetes (MESH:D003924), overweight (MESH:D050177), Type 2DM (MESH:D006969), gastrointestinal (MESH:D005767), Diabetes (MESH:D003920), Hypoglycemia (MESH:D007003), Type 2 DM (MESH:D009223), gastrointestinal side effects (MESH:D064420), Weight reduction (MESH:D015431), GI losses (MESH:D016388), complications (MESH:D008107), inflammatory disease (MESH:D007249), hypertension (MESH:D006973), dyslipidemia (MESH:D050171), nutritional deficiencies (MESH:D044342)
- **Chemicals:** metformin (MESH:D008687), sulphonylurea (MESH:D013453), exenatide (MESH:D000077270), lipids (MESH:D008055), carbohydrates (MESH:D002241), GLP-1agonists (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12960479/full.md

## References

50 references — full list in the complete paper: https://tomesphere.com/paper/PMC12960479/full.md

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Source: https://tomesphere.com/paper/PMC12960479