Increased risk of MAFLD and Liver Fibrosis in Inflammatory Bowel Disease Independent of Classic Metabolic Risk

Juan Carlos Rodriguez-Duque1, José Luis Calleja2, Paula Iruzubieta1

  • 1Gastroenterology and Hepatology Department, University Hospital Marqués de Valdecilla, Santander, Spain; Group of Clinical and Translational Research in Digestive Diseases Infection, Immunity and Digestive Pathology Group, Research Institute Marqués de Valdecilla (IDIVAL), Santander, Spain.

Abstract

Insights

Metabolic-associated fatty liver disease (MAFLD) and liver fibrosis are common in inflammatory bowel disease (IBD) patients. IBD itself is a significant risk factor for MAFLD and advanced liver fibrosis, independent of traditional metabolic factors.

Area of Science:

  • Hepatology
  • Gastroenterology
  • Internal Medicine

Background:

  • Conflicting evidence exists on the prevalence and risk factors of metabolic-associated fatty liver disease (MAFLD) in patients with inflammatory bowel disease (IBD).
  • Understanding these associations is crucial for patient management and risk stratification.

Purpose of the Study:

  • To determine the prevalence of MAFLD in patients with IBD.
  • To identify risk factors associated with MAFLD and advanced liver fibrosis in IBD patients.

Main Methods:

  • A cross-sectional, case-control study involving 831 IBD patients and 1718 general population controls.
  • MAFLD was diagnosed using controlled attenuation parameter (CAP); advanced liver fibrosis was assessed by transient elastography.
  • Liver biopsies were performed when significant fibrosis was suspected.

Main Results:

  • MAFLD prevalence was 42.00% in IBD patients versus 32.77% in controls (P < .001).
  • Advanced liver fibrosis prevalence was 9.50% in IBD patients versus 2.31% in controls (P < .001).
  • IBD diagnosis was an independent predictor of MAFLD (aOR, 1.99) and advanced liver fibrosis (aOR, 5.55).

Conclusions:

  • MAFLD and liver fibrosis are highly prevalent in IBD patients.
  • IBD is an independent risk factor for MAFLD and advanced liver fibrosis, even without classic metabolic risk factors.

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