Your browser doesn't support javascript.
loading
The overlap with metabolic dysfunction-associated steatotic liver disease negatively affects outcomes of primary biliary cholangitis.
Hernández-Pérez, María; Riado, Daniel; Pena, Eva; Méndez, Carmen; Pinedo, Fernando; Ramos, Paloma; Castillo, Pilar; Romero, Miriam; Fernández-Rodríguez, Conrado; Olveira, Antonio.
Afiliação
  • Hernández-Pérez M; Gastroenterology and Hepatology Department, La Paz University Hospital, Madrid, Spain.
  • Riado D; Gastroenterology and Hepatology Department, Alcorcón Foundation University Hospital, Alcorcón, Spain.
  • Pena E; Pathology Department, La Paz University Hospital, Madrid, Spain.
  • Méndez C; Pathology Department, La Paz University Hospital, Madrid, Spain.
  • Pinedo F; Pathology Department, Alcorcón Foundation University Hospital, Alcorcón, Spain.
  • Ramos P; Pathology Department, Alcorcón Foundation University Hospital, Alcorcón, Spain.
  • Castillo P; Gastroenterology and Hepatology Department, La Paz University Hospital, Madrid, Spain.
  • Romero M; Gastroenterology and Hepatology Department, La Paz University Hospital, Madrid, Spain.
  • Fernández-Rodríguez C; Gastroenterology and Hepatology Department, Alcorcón Foundation University Hospital, Alcorcón, Spain.
  • Olveira A; Universidad Rey Juan Carlos, Alcorcón, Madrid, Spain.
Aliment Pharmacol Ther ; 60(5): 613-619, 2024 Sep.
Article em En | MEDLINE | ID: mdl-38924185
ABSTRACT
BACKGROUND AND

AIMS:

The relationship between primary biliary cholangitis (PBC) and metabolic dysfunction-associated steatotic liver disease, and its impact on treatment 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 to Non-Alcoholic Steatohepatitis Clinical Research Network. Diagnosis of metabolic dysfunction-associated steatotic liver disease was established when steatosis exceeded 5%, along with at least one metabolic risk factor. Patients with specific aetiologies of steatosis, other liver diseases, incomplete results and inadequate treatment with ursodeoxycholic acid were excluded. Data from patients initiating second-line treatment were censored. Treatment response was assessed using the Toronto, Paris II and AST-to-platelet at 12-month criteria. The UK PBC and Globe scores, and liver events were utilized as outcome measures.

RESULTS:

The study included 129 patients, 36 showing histologically confirmed overlap between PBC and steatosis. Patients with overlap showed worse prognosis according 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 mortality and liver transplant were more prevalent in the overlap group (p = 0.001). In the multivariate analysis, steatosis, dyslipidaemia and advanced fibrosis were independently associated to worse outcomes.

CONCLUSIONS:

Our findings suggest that metabolic dysfunction-associated steatotic liver disease worsens the prognosis of PBC.
Assuntos

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Cirrose Hepática Biliar Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Aliment Pharmacol Ther Assunto da revista: FARMACOLOGIA / GASTROENTEROLOGIA / TERAPIA POR MEDICAMENTOS Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Espanha

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Cirrose Hepática Biliar Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Aliment Pharmacol Ther Assunto da revista: FARMACOLOGIA / GASTROENTEROLOGIA / TERAPIA POR MEDICAMENTOS Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Espanha