The overlap with metabolic dysfunction-associated steatotic liver disease negatively affects outcomes of primary biliary cholangitis

dc.contributor.authorHernández-Pérez, María
dc.contributor.authorRiado, Daniel
dc.contributor.authorPena, Eva
dc.contributor.authorMéndez, Carmen
dc.contributor.authorPinedo, Fernando
dc.contributor.authorRamos, Paloma
dc.contributor.authorCastillo, Pilar
dc.contributor.authorRomero, Miriam
dc.contributor.authorFernández-Rodríguez, Conrado
dc.contributor.authorOlveira, Antonio
dc.date.accessioned2024-09-24T07:49:43Z
dc.date.available2024-09-24T07:49:43Z
dc.date.issued2024-06-25
dc.descriptionThis study received a research grant support from Advanz-Phrama to the CFR institutiones
dc.description.abstractBackground and Aims: The relationship between primary biliary cholangitis (PBC)and metabolic dysfunction-associated steatotic liver disease, and its impact on treat-ment response and prognosis, remains underexplored.Methods: Patient cohort from two centres comprising long-term follow-up data.All patients had histologically confirmed PBC. Biopsies were classified according toNon-Alcoholic Steatohepatitis Clinical Research Network. Diagnosis of metabolicdysfunction-associated steatotic liver disease was established when steatosis ex-ceeded 5%, along with at least one metabolic risk factor. Patients with specific aetiol-ogies of steatosis, other liver diseases, incomplete results and inadequate treatmentwith ursodeoxycholic acid were excluded. Data from patients initiating second-linetreatment were censored. Treatment response was assessed using the Toronto, ParisII and AST-to-platelet at 12-month criteria. The UK PBC and Globe scores, and liverevents were utilized as outcome measures.Results: The study included 129 patients, 36 showing histologically confirmed over-lap between PBC and steatosis. Patients with overlap showed worse prognosis ac-cording to Paris II (61.1% vs. 33.3%, p = 0.004), Toronto (52.5% vs. 24.7%, p = 0.002),AST-to-platelet 12-month >0.54 (36.1% vs. 17.2%, p = 0.021), Globe >0.30 (49.2% vs.29.2%, p = 0.033) and UK PBC at 5, 10 and 15 years (p ≤ 0.001). Liver-related mortalityand liver transplant were more prevalent in the overlap group (p = 0.001). In the mul-tivariate analysis, steatosis, dyslipidaemia and advanced fibrosis were independentlyassociated to worse outcomes.Conclusions: Our findings suggest that metabolic dysfunction-associated steatoticliver disease worsens the prognosis of PBCes
dc.identifier.citationHernández-Pérez M, Riado D, Pena E, Méndez C, Pinedo F, Ramos P, et al. The overlap with metabolic dysfunction-associated steatotic liver disease negatively affects outcomes of primary biliary cholangitis. Aliment Pharmacol Ther. 2024; 60: 613–619. https://doi.org/10.1111/apt.18134es
dc.identifier.doi10.1111/apt.18134es
dc.identifier.issn1365-2036 (online)
dc.identifier.issn0269-2813 (print)
dc.identifier.urihttps://hdl.handle.net/10115/39770
dc.language.isoenges
dc.publisherWileyes
dc.rightsAtribución-NoComercial 4.0 Internacional*
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/*
dc.titleThe overlap with metabolic dysfunction-associated steatotic liver disease negatively affects outcomes of primary biliary cholangitises
dc.typeinfo:eu-repo/semantics/articlees

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