# A Narrative Review on GLP-1 Receptor Agonists for Obesity in Older Women: Maximizing Weight Loss While Preserving Lean Mass

**Authors:** Federica Moscucci, Francesco Baratta, Daniele Pastori, Danilo Menichelli, Anna Vittoria Mattioli, Sabina Gallina, Ilaria Lospinuso, Susanna Sciomer, Gianfranco Piccirillo, Giovambattista Desideri

PMC · DOI: 10.3390/nu18040632 · 2026-02-14

## TL;DR

This review explores how GLP-1 receptor agonists help older women lose weight while minimizing muscle loss, offering strategies to balance weight loss with muscle preservation.

## Contribution

The paper provides a comprehensive framework for using GLP-1 RAs in older women, emphasizing personalized strategies to prevent sarcopenia.

## Key findings

- Older women using GLP-1 RAs achieved 10–20% sustained weight loss with cardiometabolic improvements.
- Muscle loss risk with GLP-1 RAs highlights the need for interventions like physical activity and dietary changes.
- Combination therapies can help maintain muscle strength during weight loss in older women.

## Abstract

Obesity in women over 65 represents a growing clinical challenge, particularly due to its association with increased risks of cardiovascular disease, osteoarthritis, frailty, sleep-breathing disorders, and sarcopenia. The prevalence of obesity in this demographic is compounded by age-related metabolic changes and declining physical activity. In this context, glucagon-like peptide-1 receptor agonists (GLP-1 RAs), such as semaglutide and tirzepatide, have emerged as promising pharmacological treatments for weight loss, showing substantial efficacy in reducing body weight and improving metabolic health. However, their use in older populations warrants careful consideration due to the potential risk of muscle loss, which may exacerbate sarcopenia and frailty. This review synthesizes current evidence on the efficacy of GLP-1 RAs for weight loss in older women, exploring both the metabolic benefits and potential risks, particularly with regard to muscle mass preservation. We discuss the mechanisms behind muscle loss associated with GLP-1 RAs, focusing on the balance between fat reduction and the preservation of lean body mass. In phase 3 trials, women aged ≥ 65 years achieved sustained weight loss of 10–20%, with consistent cardiometabolic improvements. Furthermore, we propose practical strategies to mitigate sarcopenia, including physical activity interventions, dietary modifications, and combination therapies aimed at maintaining muscle strength while promoting weight loss. By examining clinical trial data, real-world evidence, and physiological mechanisms, this narrative review aims to provide a comprehensive framework for personalized and safe therapeutic decision-making, addressing the unique needs of older women with obesity.

## Linked entities

- **Proteins:** GCG (glucagon)
- **Chemicals:** semaglutide (PubChem CID 56843331), tirzepatide (PubChem CID 163285897)
- **Diseases:** obesity (MONDO:0011122), cardiovascular disease (MONDO:0004995), osteoarthritis (MONDO:0005178)

## Full-text entities

- **Genes:** 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}, MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}, GIP (gastric inhibitory polypeptide) [NCBI Gene 2695]
- **Diseases:** gastrointestinal discomfort (MESH:D005767), diabetes (MESH:D003920), weakness (MESH:D018908), malignancies (MESH:D009369), decline in functional (MESH:D060825), myocardial infarction (MESH:D009203), cardiovascular disease (MESH:D002318), insulin resistance (MESH:D007333), dehydration (MESH:D003681), Weight Loss (MESH:D015431), metabolic syndrome (MESH:D024821), postprandial hyperglycemia (MESH:D006943), injury to (MESH:D014947), Sarcopenia (MESH:D055948), inflammation (MESH:D007249), muscle atrophy (MESH:D009133), muscle (MESH:D019042), muscle hypertrophy (MESH:C536106), Mitochondrial dysfunction (MESH:D028361), geriatric syndrome (MESH:D013577), hypertension (MESH:D006973), fractures (MESH:D050723), malnutrition (MESH:D044342), sleep-breathing disorders (MESH:D012891), gastrointestinal distress (MESH:D012128), fat (MESH:D004620), metabolic (MESH:D008659), osteoarthritis (MESH:D010003), mobility limitations (MESH:D051346), chronic (MESH:D002908), frail (MESH:D000073496), cognitive decline (MESH:D003072), loss of muscle mass (MESH:C536030), nausea (MESH:D009325), depression (MESH:D003866), Obesity (MESH:D009765), chronic pain (MESH:D059350), adiposity (MESH:D018205), loss of independence (MESH:D064129), falls (MESH:C537863), type 2 diabetes (MESH:D003924), Lean Mass Loss (MESH:D013851), weight gain (MESH:D015430), stroke (MESH:D020521), appetite (MESH:D001068), fatigue (MESH:D005221), Muscle Loss (MESH:D009135)
- **Chemicals:** carbohydrates (MESH:D002241), GLP-1RAs (-), acid (MESH:D000143), essential amino acid (MESH:D000601), blood glucose (MESH:D001786), glucose (MESH:D005947), RAs (MESH:D011883), Leucine (MESH:D007930), lipid (MESH:D008055)
- **Species:** Homo sapiens (human, species) [taxon 9606]

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Source: https://tomesphere.com/paper/PMC12943638