# Association of Sarcopenia with Lower Adiponectin Levels and Reduced Estimated Appendicular Lean Mass in Patients with Metabolic Syndrome: A Cross-Sectional Study

**Authors:** Juan Antonio Suárez-Cuenca, Pablo Zermeño-Ugalde, Diana Elisa Díaz-Jiménez, Juan Antonio Pineda-Juárez, Deyanhira Palacios-Colunga, Alejandro Hernández-Patricio, Eduardo Vera-Gómez, Areli Romero-López, María Fernanda Kuri-Pineda, Andrea Ramírez-Coyotecatl, Dulce Cecilia Vázquez-Ramos, José Gutiérrez-Salinas, Silvia García, Christian Alejandro Delaflor-Wagner, Christian Gabriel Toledo-Lozano, Luis Montiel-López, María Angélica Díaz-Aranda, Alberto Melchor-López

PMC · DOI: 10.3390/diseases14020072 · Diseases · 2026-02-14

## TL;DR

This study finds that sarcopenia in metabolic syndrome patients is linked to lower adiponectin levels and reduced muscle mass, suggesting a vulnerable condition.

## Contribution

The study identifies a novel association between sarcopenia markers and adiponectin levels in metabolic syndrome patients.

## Key findings

- Sarcopenia is frequent in metabolic syndrome patients and associated with lower adiponectin levels.
- Estimated appendicular lean mass correlates with phase angle and predicts higher phase angle values.
- Sarcopenic patients had lower brachial circumference and adiponectin levels compared to non-sarcopenic patients.

## Abstract

Background: Sarcopenia is a progressive muscle disorder associated with metabolic syndrome (MS), in which early impairments in muscle strength and quality precede muscle mass loss. Simple, non-invasive measures such as handgrip strength, estimated appendicular skeletal muscle mass (eASM), and phase angle (PA) may aid early detection, while adipokines link muscle dysfunction to metabolic regulation. Objective: In the present study, we aimed to evaluate the association between sarcopenia markers and PA in patients with MS. Methods: A cross-sectional study was conducted in patients with MS, at a third-level hospital in Mexico City. Sarcopenia was assessed by handgrip strength and eASM; body composition and PA were measured using bioelectrical impedance; and plasma adipokines were quantified by ELISA. Results: Seventy-four (mean age, 57.7 years; 75% female; BMI, 32.5 kg/m2) participants with MS were included. Handgrip strength correlated with eASM (r = 0.64; p < 0.01) and PA (rho = 0.43; p < 0.01), and eASM also correlated with PA (rho = 0.40; p < 0.01) and predicted higher PA values (OR = 2.74; p = 0.042). The sarcopenic subgroup had lower brachial circumference and plasma adiponectin. Conclusions: Sarcopenia is frequent in MS and associated with lower adiponectin, suggesting a vulnerable condition. Functional/structural markers of sarcopenia showed significant correlation with PA, whereas combined methods may enhance the early detection and management of muscle deterioration in metabolic disease.

## Linked entities

- **Diseases:** metabolic syndrome (MONDO:0000816)

## Full-text entities

- **Genes:** ADIPOR1 (adiponectin receptor 1) [NCBI Gene 51094] {aka ACDCR1, CGI-45, CGI45, PAQR1, TESBP1A}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, RETN (resistin) [NCBI Gene 56729] {aka ADSF, FIZZ3, RENT, RETN1, RSTN, XCP1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, IL1RN (interleukin 1 receptor antagonist) [NCBI Gene 3557] {aka CRMO2, DIRA, ICIL-1RA, IL-1RN, IL-1ra, IL-1ra3}, ADIPOR2 (adiponectin receptor 2) [NCBI Gene 79602] {aka ACDCR2, PAQR2}, LEP (leptin) [NCBI Gene 3952] {aka LEPD, OB, OBS}, ADIPOQ (adiponectin, C1Q and collagen domain containing) [NCBI Gene 9370] {aka ACDC, ACRP30, ADIPQTL1, ADPN, APM-1, APM1}, IRS1 (insulin receptor substrate 1) [NCBI Gene 3667] {aka HIRS-1}
- **Diseases:** eASM (MESH:D001259), muscle (MESH:D019042), mitochondrial damage (MESH:D028361), injury to (MESH:D014947), Sarcopenia (MESH:D055948), chronic liver disease (MESH:D008107), inflammation (MESH:D007249), MS (MESH:D024821), head and neck cancer (MESH:D006258), atrophic (MESH:D020966), chronic renal failure (MESH:D007676), cancer (MESH:D009369), COPD (MESH:D029424), impairments in muscle strength and quality (MESH:D009135), chronic heart failure (MESH:D006333), obesity (MESH:D009765), PA (MESH:D000210), loss of muscle mass and (MESH:C536030), HIV (MESH:D015658), metabolic disease (MESH:D008659), lipid abnormalities (MESH:D011017)
- **Chemicals:** BMS2032-2 (-), triglycerides (MESH:D014280), lipid (MESH:D008055), glucose (MESH:D005947), cholesterol (MESH:D002784), reactive oxygen species (MESH:D017382), alcohol (MESH:D000438)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** BMS215-2TEN — Homo sapiens (Human), Endometrial clear cell adenocarcinoma, Cancer cell line (CVCL_E063)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12939164/full.md

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12939164/full.md

## References

27 references — full list in the complete paper: https://tomesphere.com/paper/PMC12939164/full.md

---
Source: https://tomesphere.com/paper/PMC12939164