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March 28, 2026BMC Gastroenterology0 citationsOpen Access

Metabolic dysfunction-associated steatohepatitis in the real world: clinical burden, disease progression, and risk stratification with non-invasive tests

CSClaudio SartiniRHRonald HerreraFMFaizan Mazhar

Key Points

  • This research aims to understand the clinical burden and mortality patterns of metabolic dysfunction-associated steatohepatitis (MASH) through non-invasive tests.
  • Analyzed 18,710 adults with MASH using data from Optum Market Clarity
  • Assessed associations between comorbidities, non-invasive tests, liver outcomes, and mortality
  • Employ Fine-Gray models for survival analysis
  • Mortality rates were 0.82 per 100 person-years for non-cirrhosis, 3.50 for compensated cirrhosis, and 11.28 for decompensated cirrhosis
  • Progression to cirrhosis in non-cirrhosis patients occurred at a rate of 5.71 per 100 person-years
  • A FIB-4 score > 2.67 indicated a seven-fold increase in mortality risk

Abstract

Metabolic dysfunction-associated steatohepatitis (MASH) increases risk of liver-related outcomes, yet comorbidities and mortality patterns remain unclear. Using Optum Market Clarity, we identified adults with MASH and assessed associations of comorbidities and noninvasive tests with liver outcomes and mortality via Fine-Gray models. 18,710 patients were identified (73.5% without cirrhosis, 9.0% with compensated cirrhosis (CC), 17.8% with decompensated cirrhosis, DC). The mortality rate was 0.82, 3.50, and 11.28 per 100 person-years (PY) for the non-cirrhosis, CC and DC subgroups, respectively. Among those without cirrhosis, progression to cirrhosis occurred at a rate of 5.71 per 100 PY. A FIB-4 score > 2.67 vs. ≤ 2.67 was associated with a seven-fold increase in mortality risk (adjusted hazard ratio aHR = 7.06; 95% confidence interval CI = 6.37–7.83). Elevated AST levels (> 40 U/L vs. ≤40 U/L; aHR = 1.38, 95% CI = 1.24–1.53) and living with ≥ 3 comorbidities (vs. none; HR:1.93, 95% CI 1.47–2.54) were also associated with increased mortality. Our findings highlight the impact of MASH on patients and show how accessible noninvasive tests can identify those at highest risk, empowering timely care at every stage.

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Cite This Study

Sartini et al. (2026) studied this question.

synapsesocial.com/papers/69c772818bbfbc51511e3052https://doi.org/10.1186/s12876-026-04745-1
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