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Nutritional, functional, and psychological considerations for incretin-based therapies in adults—an EASO, EFAD, and ECPO Consensus Statement

The Lancet Diabetes & Endocrinology·July 8
Endocrinology & MetabolismPractice changingObesityType 2 DiabetesConsensus StatementDual GLP-1–GIP Receptor AgonistGLP-1 Receptor AgonistAdultDulaglutideExenatideLiraglutideSemaglutideTirzepatide

Summary

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What was studied

This EASO–EFAD–ECPO Consensus Statement synthesizes evidence and provides pragmatic guidance on nutritional (protein targets, dietary quality, micronutrients, GI side-effect mitigation), functional (fat-free mass preservation, resistance exercise), and psychological (food reward, eating disorders, identity, mental health screening) considerations for adults receiving incretin-based therapies—specifically GLP-1 receptor agonists and dual GLP-1–GIP receptor agonists—for obesity management.

Key findings

The statement recommends: adequate protein intake and progressive resistance exercise to mitigate fat-free mass loss during rapid weight loss; routine monitoring of diet quality, micronutrient status (including thiamine), and functional measures (e.g., handgrip strength); psychological screening for eating disorders and mental health challenges; and shared decision-making around dose titration and discontinuation given the risk of weight regain on cessation.

Study limitations

- Based on expert consensus rather than original trial data; recommendations are pragmatic and evidence-graded from a heterogeneous literature. - Longitudinal data on micronutrient status, macronutrient requirements, and musculoskeletal outcomes specifically during incretin-based therapy are sparse. - Disparities in access and representation (sex, race, BMI) in underlying clinical trials limit generalizability across populations.

Clinical implications

When prescribing GLP-1 or dual GLP-1–GIP agonists for obesity, proactively target adequate protein intake, prescribe progressive resistance training, and screen for micronutrient deficiencies and eating disorders at baseline and throughout treatment. Discuss the risk of weight regain and muscle loss with patients when considering dose changes or stopping therapy.

Caveats

  • Full text was not accessible; summary is based on the abstract and publisher page only, which may omit specific numeric recommendations (e.g., exact protein targets, screening tool thresholds) detailed in the full document.
  • The 'practice_changing' impact flag reflects the breadth and clinical scope of EASO/EFAD/ECPO guidance on a rapidly evolving therapy class, not a single pivotal trial result.
  • This is a consensus statement, not an original research study—no primary sample size or effect sizes are reported; level of evidence reflects expert opinion.

Related Questions

Explore related topics

How much protein should patients take daily while on semaglutide or tirzepatide for obesity?What resistance exercise program is recommended to prevent muscle loss during GLP-1 receptor agonist therapy?How should clinicians screen for eating disorders and micronutrient deficiencies in patients on incretin-based obesity therapy?

Publication Details

Year
2026
Journal
The Lancet Diabetes & Endocrinology
Source
View article
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