All research
Semaglutide 2026-06-01 PubMed

Health-behavior and lifestyle therapy significantly increases liraglutide adherence and BMI reduction in adolescents with obesity.

Combining GLP-1 Receptor Agonists and Health-Behaviour and Lifestyle Therapy Yields Higher Adherence and Reduces Session Needs for Successful Weight Management in Adolescence: An Observational Real-World Single-Center Study.

Background

Managing pediatric obesity is challenging, with current treatments often facing issues like poor adherence and variable efficacy. While glucagon-like peptide-1 receptor agonists (GLP-1RAs) like liraglutide have shown promise, their real-world effectiveness in youth, particularly concerning the role of concurrent health behavior and lifestyle treatment (HBLT), remains underexplored. This gap highlights the need to understand how HBLT impacts GLP-1RA outcomes, especially given the chronic nature of obesity and the importance of sustained engagement for long-term success. Addressing this could optimize treatment strategies and improve patient persistence.

Study Design

This observational, real-world, single-center study retrospectively analyzed 51 patients aged 8-18 years with obesity receiving liraglutide. Patients were categorized into continuers, discontinuers, or those who switched to semaglutide or metabolic-bariatric surgery. All participants were offered multidisciplinary HBLT, consecutively allocated to either high-frequency (HF) HBLT (≥26 contact hours/year) or low-frequency obesity medication (OM)-specific HBLT (9 contacts of 0.5 h/year). The primary endpoints included BMI reduction and liraglutide treatment continuation rates over an average follow-up of 9.7 ± 6.6 months.

Results

After an average of 9.7 ± 6.6 months, a BMI reduction of ≥5% was observed in 37.3% of patients, and ≥10% in 13.7%. The relative change in BMI was significantly higher in liraglutide continuers compared to discontinuers (-6.7% ± 7.5% vs. -0.7% ± 5.1%, p=0.03). While 39.2% of patients continued liraglutide, 33.3% discontinued, primarily due to gastrointestinal symptoms. Another 27.4% switched treatment or underwent surgery. The most impactful finding was the strong association between HBLT and treatment persistence: > Patients receiving combined HBLT and liraglutide had markedly higher odds of continuation (OR 18.5, 95% CI 2.0-929.8, p<0.01). Furthermore, patients receiving OM-specific HBLT showed a trend towards greater BMI reduction compared to HF-HBLT (-6.9% ± 7.2% vs. -4.0% ± 6.6%), suggesting that even targeted, lower-frequency HBLT can be highly effective.

Key Findings

  • Liraglutide reduced BMI by ≥5% in 37.3% of adolescents and ≥10% in 13.7% over 9.7 months.
  • Patients continuing liraglutide showed significantly greater BMI reduction (-6.7% vs. -0.7%, p=0.03).
  • Combined HBLT with liraglutide increased the odds of treatment continuation by 18.5x (p<0.01).
  • OM-specific HBLT trended towards higher BMI reduction (-6.9%) compared to HF-HBLT (-4.0%).
  • Gastrointestinal symptoms were the main reason for liraglutide discontinuation in 33.3% of patients.

Why It Matters

This study underscores that integrating structured health behavior and lifestyle therapy (HBLT) is crucial for maximizing the effectiveness and adherence of GLP-1RAs like liraglutide in adolescents with obesity. It suggests that GLP-1RAs are not standalone solutions but are significantly potentiated by concurrent lifestyle support. For clinicians and biohackers, this implies that simply prescribing a GLP-1RA without robust HBLT may lead to suboptimal outcomes and higher discontinuation rates. The finding that even lower-frequency, targeted HBLT can be highly effective offers a practical, scalable approach. Consider HBLT an essential co-intervention, not an optional add-on, when using GLP-1RAs for weight management in youth. This could inform future protocol designs, emphasizing comprehensive care models.


liraglutide semaglutide pediatric-obesity obesity glp-1-agonist lifestyle-intervention
Source: pubmed:42222894 · Ingested 2026-06-01 · Digest: gemini-2.5-flash