Nutritional Approaches to Enhance GLP-1 Analogue Therapy in Obesity: A Narrative Review
Glucagon-like peptide-1 receptor agonists (GLP-1RAs) are highly effective in the management of obesity; however, their efficacy and tolerability may be further optimized through complementary nutritional strategies. Such interventions may address key challenges associated with GLP-1RA therapy, including gastrointestinal adverse effects, lean mass loss, and reduced long-term adherence leading to weight regain. Evidence from preclinical and clinical studies indicates that omega-3 polyunsaturated fatty acids may enhance the metabolic benefits of GLP-1RAs and attenuate lean mass loss, primarily via anti-inflammatory pathways and modulation of protein synthesis. Synergistic effects have also been reported with other bioactive compounds—such as flavonoids and anthocyanins, which improve metabolic outcomes; probiotics and prebiotics, which may alleviate gastrointestinal intolerance; and high-quality protein sources, which support body composition preservation. Collectively, these findings suggest that nutritional adjuncts may complement GLP-1RA therapies through convergent physiological mechanisms, including the regulation of inflammation, gut microbiome composition, and cellular metabolism. While current data highlight the promise of integrated pharmaco-nutritional strategies as adjuncts to GLP-1-based obesity therapy, further randomized controlled trials are needed to establish the most effective interventions and protocols.
Authors
- José João Name (ORCID: https://orcid.org/0000-0001-7255-0405)
- Ana Carolina Remondi Souza (ORCID: https://orcid.org/0000-0001-8666-7436)
- Caroline de Menezes (ORCID: https://orcid.org/0000-0002-0146-3707)
- Andréa Rodrigues Vasconcelos (ORCID: https://orcid.org/0000-0001-7549-6408)
- Denise Dias
- Ilan Iginio da SILVA
Publication Details
- Journal
- Obesities
- Published
- 2025-12-02
- DOI
- https://doi.org/10.3390/obesities5040088
- Primary Topic
- Diabetes Treatment and Management
- Type
- article
- Field-Weighted Citation Impact
- 0.00