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October 23, 2025Clinical and Experimental Medicine5 citationsOpen Access

Sarcopenic visceral obesity in patients with metabolic dysfunction-associated steatotic liver disease (MASLD)

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MEMaha ElsabaawyARAmr RagabAAA Abdel-Razek

Key Points

  • Sarcopenic visceral obesity was found in 42.5% of patients, indicating a high metabolic risk profile.
  • Multivariate analysis indicated sarcopenic visceral obesity independently predicted advanced fibrosis, with an odds ratio of 2.5.
  • Assessment included MRI-based visceral fat area, bioelectrical impedance analysis for sarcopenia, and magnetic resonance elastography for fibrosis.
  • Introducing a tiered risk classification highlights the need for personalized management strategies for MASLD patients.

Abstract

Abstract Sarcopenic visceral obesity (SVO) has emerged as a high-risk metabolic phenotype in metabolic dysfunction-associated steatotic liver disease (MASLD). This study aimed to define the prevalence and metabolic implications of MRI-defined SVO in MASLD, evaluate its association with liver fibrosis, cardiovascular risk, and introduce a novel tier-based classification for risk stratification. In this cross-sectional study, 334 adults with MASLD underwent comprehensive phenotyping. Sarcopenia was assessed by bioelectrical impedance analysis, while visceral obesity was quantified via MRI-based visceral fat area (VFA ≥ 100 cm 2 ). Liver fibrosis was evaluated using non-invasive indices and confirmed in a subset by magnetic resonance elastography (MRE). Participants were stratified into SVO and non-SVO groups, and further categorized into Red, Yellow, or Green tiers based on fibrosis stage and cardiovascular risk. SVO was present in 42.5% of MASLD patients, with higher prevalence among women and individuals with BMI ≥ 40. SVO was associated with significantly worse metabolic profiles (HOMA-IR: 6.2 ± 2.8, p < 0.001), advanced fibrosis (FIB-4: 2.3 ± 1.4, p = 0.003), and higher cardiovascular risk (ASCVD ≥ 7.5%: 65%, p < 0.001). In multivariate analysis, SVO independently predicted advanced fibrosis (OR = 2.5, p = 0.002). Importantly, a tier-based classification model identified a high-risk “Red Tier” group (100% F3–F4 fibrosis, 100% diabetes). This is the first study in a Middle Eastern MASLD cohort to combine MRI-based adiposity assessment with validated sarcopenia criteria to define SVO and demonstrate its prognostic relevance. The introduction of a tiered risk framework integrating SVO, fibrosis, and ASCVD risk represents a novel approach to personalized MASLD care and support targeted decision-making.

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Cite This Study

Elsabaawy et al. (2025) studied this question.

synapsesocial.com/papers/68f9a0eb8ea8f2f37ee94b1bhttps://doi.org/10.1007/s10238-025-01865-y
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