Short- and Medium-Chain Fatty Acid Profiles in Biopsy-Proven Metabolic Dysfunction-Associated Steatotic Liver Disease: A Cross-Sectional Study
Background/Objectives: Metabolic dysfunction-associated steatotic liver disease (MASLD) is a common metabolic liver disease with increasing prevalence worldwide. Increasing evidence suggests that short-chain fatty acids (SCFAs) play an important role in MASLD. Medium-chain fatty acids (MCFAs), although less studied, may also contribute to MASLD pathogenesis. The aim of this study was to evaluate plasma SCFA and MCFA profiles across the MASLD histological spectrum and their associations with clinical, biochemical, and histopathological features of disease severity. Methods: We included 115 adults with obesity undergoing bariatric surgery. Intraoperative liver biopsies were assessed using the Steatosis, Activity, Fibrosis (SAF) score. Participants were classified as no MASLD (n = 26), metabolic dysfunction-associated steatotic liver (MASL; n = 42), or metabolic dysfunction-associated steatohepatitis (MASH; n = 47). Six SCFAs and two MCFAs were quantified in plasma by liquid chromatography–mass spectrometry. Results: Patients with MASH showed lower acetate and higher hexanoate plasma levels than those without MASLD. Acetate was inversely associated with ALT, AST, GGT, glucose, HbA1c, cytokeratin-18, SAF score, steatosis and lobular inflammation, whereas hexanoate was positively associated with SAF score and lobular inflammation. Higher acetate concentrations were independently associated with lower odds of MASH (OR 0.973; p = 0.040), while ALT levels were independently associated with increased odds of MASH (OR 1.083, p = 0.001). Conclusions: MASH in patients with obesity is characterized by a distinct circulating fatty acid profile, with reduced acetate and increased hexanoate. Lower acetate levels were independently associated with MASH and markers of metabolic and histological disease severity.
Authors
- Eliana Mariño (ORCID: https://orcid.org/0000-0001-5371-8778)
- José Carlos Fernández‐García (ORCID: https://orcid.org/0000-0003-2229-8488)
- Bruno Ramos‐Molina (ORCID: https://orcid.org/0000-0001-6804-5449)
- Lidia Sánchez‐Alcoholado (ORCID: https://orcid.org/0000-0002-5410-1638)
- Esteban N. Gurzov (ORCID: https://orcid.org/0000-0003-4642-0273)
- María Ángeles Núñez‐Sánchez (ORCID: https://orcid.org/0000-0002-8938-2767)
- Inmaculada Ros‐Madrid (ORCID: https://orcid.org/0000-0001-6862-1012)
- Mercedes Ferrer‐Gómez (ORCID: https://orcid.org/0000-0003-4617-0219)
- Virginia Esperanza Fernández-Ruiz (ORCID: https://orcid.org/0000-0002-3976-3967)
- Alicia González-González (ORCID: https://orcid.org/0000-0001-8020-2531)
- María Antonia Martínez‐Sánchez (ORCID: https://orcid.org/0000-0001-9750-4237)
- María Dolores Frutos (ORCID: https://orcid.org/0000-0002-2111-4715)
- Carlos Manuel Martínez (ORCID: https://orcid.org/0000-0003-3307-1326)
- Sara Rico‐Chazarra (ORCID: https://orcid.org/0009-0002-4490-1866)
- Rosario Paloma Cano-Mármol (ORCID: https://orcid.org/0000-0003-2098-7626)
- Antonio Silva
Institutions
- Université Libre de Bruxelles (BE)
- Instituto de Salud Carlos III (ES)
- Centro de Investigación Biomédica en Red Diabetes y Enfermedades Metabólicas Asociadas (ES)
- Hospital Regional Universitario de Málaga (ES)
- Instituto Murciano de Investigación Biosanitaria (ES)
- Andalusian Centre for Nanomedicine and Biotechnology (ES)
- Hospital Universitario Virgen de la Arrixaca (ES)
- Instituto de Investigación Biomédica de Málaga (ES)
- Universidad de Murcia (ES)
- Universidad de Extremadura (ES)
- Universidad de Málaga (ES)
Publication Details
- Journal
- Nutrients
- Published
- 2026-10-28
- DOI
- https://doi.org/10.3390/nu18213548
- Primary Topic
- Liver Disease Diagnosis and Treatment
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Fundación Séneca
- Instituto de Salud Carlos III