Peptide News Digest

#Dxa

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Research · View digest

Journal of Nutrition Review (June 20): 'Avoiding Malnutrition in the Era of GLP-1 Medications' — 25% of GLP-1 Weight Loss is Lean Mass, Calls for Protein Standards and Routine Body-Composition Endpoints in Late-Stage Trials

The Journal of Nutrition published online on June 20, 2026 a review titled 'Avoiding malnutrition in the era of GLP-1 medications: emerging evidence and opportunities for integrated nutrition care.' The review documents that approximately 25% of total weight lost on GLP-1 therapy is lean mass — a substantial proportion depending on the magnitude of weight reduction achieved — and frames disproportionate fat-free mass loss as a metabolic-health and physical-function risk independent of total weight loss. The authors call for GLP-1-specific randomized trials defining optimal protein intake stratified by age, rate of weight loss, and baseline sarcopenia risk; guidance on when supplementation may be necessary; strategies for monitoring micronutrient status; and routine incorporation of body composition assessments (DXA/BIA) and standardized muscle function measures (handgrip strength, chair-rise testing) as co-primary or key secondary endpoints in future GLP-1 RA studies.

Research · View digest

ECO 2026 Day 3 Cagrilintide Monotherapy DXA Body Composition Subgroup — 62.9% Fat Mass Selectivity

A second body-composition substudy from REDEFINE 1 presented May 14 at ECO 2026 broke out the DXA subgroup by treatment arm. At week 68, CagriSema (cagrilintide 2.4 mg + semaglutide 2.4 mg) produced -23.9% weight reduction in the DXA subgroup, compared with -16.6% on semaglutide 2.4 mg alone, -15.0% on cagrilintide 2.4 mg alone, and -2.8% on placebo. The fat-mass-to-lean-tissue ratios were favorable across all active arms: 66.9% fat-mass contribution on CagriSema, 69.7% on semaglutide, 62.9% on cagrilintide. The cagrilintide monotherapy arm is the first head-to-head body-composition signal for amylin-only therapy at clinically meaningful weight-loss levels — relevant to Zealand and Roche's petrelintide Phase 3 program and the broader amylin-versus-incretin debate.