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January 20, 2026Liver International0 citationsOpen Access

Progression to Decompensation of Severe Fibrosis Compared to Cirrhosis in MASLD : A Systematic Review and Meta‐Analysis

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RBRachael BarrettAAAnnie ArcherJCJennifer N. Cathcart

Key Points

  • This review aims to compare the progression risks of decompensated liver disease between patients with F3 and F4 fibrosis due to MASLD.
  • Conducted systematic searches across four databases
  • Two independent reviewers screened articles against predefined criteria
  • Included 29 studies focusing on various outcomes related to F3 and F4 fibrosis
  • 16%–30% of patients with F3 fibrosis progressed to major liver complications during follow-up
  • 16% of F3 fibrosis patients developed varices
  • HCC incidence in F3 fibrosis ranged from 37% to 75%
  • Pooled hazard ratios indicated significant risks for progression to major adverse liver outcomes for both F3 and F4 fibrosis

Abstract

ABSTRACT Background articles were screened by two independent reviewers against pre‐specified inclusion and exclusion criteria. Results Twenty‐nine studies were included in the review: 12 with paired liver biopsies, 2 progression to cirrhosis, 13 progression to decompensation, 2 portal hypertension in F3 fibrosis and 13 on HCC in F3 fibrosis. Rates of progression on paired biopsies were 16%–30% over varied follow‐up. Varices were found in 16% of patients with F3 fibrosis and rates of non‐cirrhotic HCC varied from 37%–75%. Pooled univariate HR for F3 progression and F4 progression to major adverse liver outcomes (MALO) were 8.15 (95% CI 3.42–19.43) and 38.16 (95% CI 11.58–125.76), respectively. Conclusions Progression to cirrhosis and decompensation events occurs in a significant proportion of patients with F3 fibrosis in MASLD. There is evidence of portal hypertension and HCC developing in F3 MASLD. Further work to identify risk groups, including those at risk of rapid progression to guide future clinical management is urgently required given the prognostic inflection of decompensated disease.

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Cite This Study

Barrett et al. (2026) studied this question.

synapsesocial.com/papers/696f1a469e64f732b51ee7cchttps://doi.org/10.1111/liv.70511
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