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

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Autores de IDIVAL

Autores ajenos al IDIVAL

  • Rodriguez-Duque JC
  • Calleja JL
  • Hernández-Conde M
  • Rivas-Rivas C
  • Vera MI
  • García-Blanco A
  • Lopez-Montejo L
  • Fernández-Lamas T
  • Rasines L
  • Frias Y

Unidades

Abstract

BACKGROUND & AIMS: There is conflicting evidence regarding the prevalence of and risk factors for metabolic-associated fatty liver disease (MAFLD) in patients with inflammatory bowel disease (IBD). We aimed to determine MAFLD prevalence and risk factors in IBD patients.METHODS: Cross-sectional, case-control study included all consecutive IBD patients treated at 2 different university hospitals. Controls were subjects randomly selected from the general population and matched by age, sex, type 2 diabetes status, and body mass index in a 1:2 ratio. MAFLD was confirmed by controlled attenuation parameter. Liver biopsies were collected when MAFLD with significant liver fibrosis was suspected. In addition, age-and fibrosis stage-paired non-IBD patients with biopsy-proven MAFLD served as a secondary control group.RESULTS: Eight hundred thirty-one IBD patients and 1718 controls were included. The prevalence of MAFLD and advanced liver fibrosis (transient elastography double dagger 9.7 kPa) was 42.00% and 9.50%, respectively, in IBD patients and 32.77% and 2.31%, respectively, in the general population (P < .001). A diagnosis of IBD was an independent predictor of MAFLD (adjusted odds ratio, 1.99; P < .001) and an independent risk factor for advanced liver fibrosis (adjusted odds ratio, 5.55; P < .001). Liver biopsies were obtained from 40 IBD patients; MAFLD was confirmed in all cases, and fibrosis of any degree was confirmed in 25 of 40 cases (62.5%). Body mass index and type 2 diabetes prevalence were significantly lower in IBD-MAFLD patients than in severity-paired patients with biopsy-proven MAFLD. CONCLUSIONS: MAFLD and liver fibrosis are particularly prevalent in IBD patients, regardless of the influence of classic metabolic risk factors.

Datos de la publicación

ISSN/ISSNe:
1542-3565, 1542-7714

CLINICAL GASTROENTEROLOGY AND HEPATOLOGY  ELSEVIER SCIENCE INC

Tipo:
Article
Páginas:
406-

Citas Recibidas en Web of Science: 29

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