Liver fibrosis index-4 does not correlate to liver elastography in patients with inflammatory bowel disease
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Ferraz-Amaro, Iván; Hernández-Camba, Alejandro; Carrillo-Palau, Marta; Hernández Álvarez-Buylla, Noemi; Vera-González, Antonia de; González-Delgado, Alejandra; Heras-Recuero, Elena; González-Gay Mantecón, Miguel Ángel
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2024Derechos
© 2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license.
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Journal of Clinical Medicine, 2024, 13, 6430
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MDPI
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Palabras clave
Inflammatory bowel disease
Ulcerative colitis
Crohn’s disease
Metabolic dysfunction-associated steatotic liver disease
Fibrosis-4 (FIB-4) index
Elastography
Resumen/Abstract
Background: Inflammatory bowel disease (IBD) is associated with an increased prevalence of metabolic dysfunction-associated steatotic liver disease (MASLD). The Fibrosis-4 (FIB-4) index is a non-invasive tool for assessing liver fibrosis that has been validated in various liver diseases. The main objective of this study was to study whether the FIB-4 index is a reliable predictor of liver fibrosis, as assessed through elastography, in patients with IBD. We additionally aimed to analyze if FIB-4 associates with IBD characteristics such as lipid profile, subclinical carotid atherosclerosis, and insulin resistance indices.
Methods: A cross-sectional study was conducted, enrolling 197 patients with IBD. Subjects underwent comprehensive clinical and laboratory evaluations. Hepatic fibrosis was assessed non-invasively using the FIB-4 index and transient elastography, while abdominal ultrasonography was performed to grade hepatic steatosis based on the degree of fat infiltration. To investigate the associations between disease characteristics and FIB-4 score and the correlation of this index to elastography, a multivariable linear regression analysis was conducted.
Results: The presence of diabetes, hypertension, and metabolic syndrome was associated with significantly higher FIB-4 levels. However, FIB-4 did not show a relationship with disease characteristics such as phenotype or activity indices. Furthermore, FIB-4 did not demonstrate a correlation with liver stiffness values measured by elastography.
Conclusions: Our findings suggest that the FIB-4 index may not be a reliable tool for assessing hepatic fibrosis in patients with IBD. This observation is particularly significant given the high prevalence of MASLD in the IBD population.
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