Steatotic Liver Disease at Primary Biliary Cholangitis Diagnosis: Association With Ursodeoxycholic Acid Response and Outcomes

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Authors: María Del Barrio, Margarita Sala, Judith Gómez, Diana Horta, Manuel Hernández-Guerra, Magdalena Salcedo, Silvia Goñi, Raquel Ríos‐León, Ángela Martínez Herreros, Jesús M. González-Santiago, J Martinez, Nerea C. Quintans
+27 more Javier Ampuero, María Dolores Antón, Margarita Fernández-de la Varga, Desamparados Escudero, Ismael El Hajra, Francisca Cuenca Alarcón, Sara Lorente, Raúl J Andrade, Mar Riveiro‐Barciela, Inmaculada Castelló, Mercè Vergara, Raisa Quiñones, Ana Arencibia Almeida, Sonia Blanco Sampascual, Carles Leal, Montserrat Garcı́a-Retortillo, Indhira Pérez-Medrano, Miguel Fernández‐Bermejo, Rosa Maria Morillas, Elena Góméz, J Tejedor-Tejada, Mercè Roget, Sergio Rodríguez‐Tajes, Marta Alonso-Peña, Ana Álvarez-Cancelo, María‐Carlota Londoño, Álvaro Díaz‐González
Cited by: 1
References: 35

Abstract

BACKGROUND AND AIM: Steatotic liver disease (SLD) is becoming increasingly prevalent, leading to a higher frequency of primary biliary cholangitis (PBC) cases coexisting with SLD. However, data on its impact in patients with PBC remain scarce. The aim is to assess the impact of SLD on treatment response and prognosis in patients with PBC receiving ursodeoxycholic acid (UDCA). METHODS: A retrospective, multicenter cohort study including patients diagnosed with PBC enrolled in the Spanish ColHai registry. RESULTS: A total of 469 patients with available data required for the study were included. Among them, 158 (33.7%) had SLD, and 124 (78.5%) met the diagnostic criteria for MASLD. Patients with PBC and SLD had lower baseline levels of alkaline phosphatase and higher liver stiffness at diagnosis. Regarding treatment response, no significant differences were observed across the different response criteria (Paris II, GLOBE, UK-PBC, deep response and complete normalization). Additionally, the presence of SLD was not associated with UDCA response at 1-year (Paris II: OR 1.04 [0.69-1.56]; GLOBE: OR 0.91 [0.58-1.44]; deep response: OR 1.08 [0.72-1.63]; complete normalization: OR 0.82 [0.52-1.30]). Baseline SLD was not associated with an increased risk of liver related-events in either the univariate analysis (HR 1.19, 95% CI 0.71-2.02) or in the different multivariate models evaluated. After inverse probability of treatment weighting (IPTW) using propensity scores, SLD still showed no significant impact on hepatic event development (HR 1.62; 95% CI 0.92-2.83). CONCLUSION: Although SLD is frequently observed in PBC, it does not appear to adversely affect UDCA response or long-term hepatic outcomes.

Fields of Study & Subjects

Liver Diseases and Immunity Drug Transport and Resistance Mechanisms Liver Disease Diagnosis and Treatment

Publication details

Journal / source
Liver International
Publisher
Wiley
Volume
46
Issue
7
Pages
e70713–e70713
Publication date
5 June 2026
Language
EN