The overlap with metabolic dysfunction-associated steatotic liver disease negatively affects outcomes of primary biliary cholangitis
dc.contributor.author | Hernández-Pérez, María | |
dc.contributor.author | Riado, Daniel | |
dc.contributor.author | Pena, Eva | |
dc.contributor.author | Méndez, Carmen | |
dc.contributor.author | Pinedo, Fernando | |
dc.contributor.author | Ramos, Paloma | |
dc.contributor.author | Castillo, Pilar | |
dc.contributor.author | Romero, Miriam | |
dc.contributor.author | Fernández-Rodríguez, Conrado | |
dc.contributor.author | Olveira, Antonio | |
dc.date.accessioned | 2024-09-24T07:49:43Z | |
dc.date.available | 2024-09-24T07:49:43Z | |
dc.date.issued | 2024-06-25 | |
dc.description | This study received a research grant support from Advanz-Phrama to the CFR institution | es |
dc.description.abstract | Background 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 PBC | es |
dc.identifier.citation | Hernández-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.18134 | es |
dc.identifier.doi | 10.1111/apt.18134 | es |
dc.identifier.issn | 1365-2036 (online) | |
dc.identifier.issn | 0269-2813 (print) | |
dc.identifier.uri | https://hdl.handle.net/10115/39770 | |
dc.language.iso | eng | es |
dc.publisher | Wiley | es |
dc.rights | Atribución-NoComercial 4.0 Internacional | * |
dc.rights.accessRights | info:eu-repo/semantics/openAccess | es |
dc.rights.uri | http://creativecommons.org/licenses/by-nc/4.0/ | * |
dc.title | The overlap with metabolic dysfunction-associated steatotic liver disease negatively affects outcomes of primary biliary cholangitis | es |
dc.type | info:eu-repo/semantics/article | es |
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