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Prognostic scores for ursodeoxycholic acid-treated patients predict graft loss and mortality in recurrent primary biliary cholangitis after liver transplantation.
Montano-Loza, Aldo J; Lytvyak, Ellina; Hirschfield, Gideon; Hansen, Bettina E; Ebadi, Maryam; Berney, Thierry; Toso, Christian; Magini, Giulia; Villamil, Alejandra; Nevens, Frederik; Van den Ende, Natalie; Pares, Albert; Ruiz, Pablo; Terrabuio, Débora; Trivedi, Palak J; Abbas, Nadir; Donato, Maria Francesca; Yu, Lei; Landis, Charles; Dumortier, Jérôme; Dyson, Jessica Katharine; van der Meer, Adriaan J; de Veer, Rozanne; Pedersen, Mark; Mayo, Marlyn; Manns, Michael P; Taubert, Richard; Kirchner, Theresa; Belli, Luca S; Mazzarelli, Chiara; Stirnimann, Guido; Floreani, Annarosa; Cazzagon, Nora; Russo, Francesco Paolo; Burra, Patrizia; Zigmound, Udi; Houri, Inbal; Carbone, Marco; Mulinacci, Giacomo; Fagiuoli, Stefano; Pratt, Daniel Stephan; Bonder, Alan; Schiano, Thomas D; Haydel, Brandy; Lohse, Ansgar; Schramm, Christoph; Rüther, Darius; Casu, Stefania; Verhelst, Xavier; Beretta-Piccoli, Benedetta Terziroli.
Afiliação
  • Montano-Loza AJ; University of Alberta, Edmonton, Alberta, Canada. Electronic address: montanol@ualberta.ca.
  • Lytvyak E; University of Alberta, Edmonton, Alberta, Canada.
  • Hirschfield G; Toronto Center for Liver Disease, UHN, Toronto, Canada.
  • Hansen BE; Dept of Epidemiology, Erasmus MC, Rotterdam, the Netherlands; IHPME, University of Toronto & Toronto Center for Liver Disease, UHN, Toronto, Canada.
  • Ebadi M; University of Alberta, Edmonton, Alberta, Canada.
  • Berney T; Geneva University Hospitals, Geneva, Switzerland.
  • Toso C; Geneva University Hospitals, Geneva, Switzerland.
  • Magini G; Geneva University Hospitals, Geneva, Switzerland.
  • Villamil A; Unidad de Autoinmunidad Hepática, Sección de Hepatología y Trasplante Hepático, Hospital Italiano de Buenos Aires, Argentina.
  • Nevens F; Division Liver and Biliopancreatic Disorders, Leuven, Belgium.
  • Van den Ende N; Division Liver and Biliopancreatic Disorders, Leuven, Belgium.
  • Pares A; University of Barcelona, Barcelona, Spain.
  • Ruiz P; Liver Unit, Hospital Clínic, Barcelona, Spain.
  • Terrabuio D; University of São Paulo School of Medicine, San Paulo, Brazil.
  • Trivedi PJ; University of Birmingham, Birmingham, United Kingdom.
  • Abbas N; University of Birmingham, Birmingham, United Kingdom.
  • Donato MF; Division of Gastroenterology and Hepatology, Fondazione IRCCS Maggiore Hospital Policlinico Milan, Italy.
  • Yu L; University of Washington, Seattle, USA.
  • Landis C; University of Washington, Seattle, USA.
  • Dumortier J; Hospices civils de Lyon, Edouard Herriot Hospital Hepatogastroenterology Unit, and University of Lyon, Lyon, France.
  • Dyson JK; Newcastle University, Newcastle, United Kingdom.
  • van der Meer AJ; Dept of Gastroenterology and Hepatology, Erasmus MC, Rotterdam, Netherlands.
  • de Veer R; Dept of Gastroenterology and Hepatology, Erasmus MC, Rotterdam, Netherlands.
  • Pedersen M; University of Texas Southwestern Medical Center, Dallas, USA.
  • Mayo M; University of Texas Southwestern Medical Center, Dallas, USA.
  • Manns MP; Hannover Medical School, Hannover, Germany.
  • Taubert R; Dept. Gastroenterology, Hepatology, Infectious Diseases and Endocrinology, Hannover Medical School, Hannover, Germany.
  • Kirchner T; Dept. Gastroenterology, Hepatology, Infectious Diseases and Endocrinology, Hannover Medical School, Hannover, Germany.
  • Belli LS; Niguarda transplant centre, Milan, Italy.
  • Mazzarelli C; Niguarda transplant centre, Milan, Italy.
  • Stirnimann G; University Hospital Inselspital, Bern, Switzerland.
  • Floreani A; University of Padova, Padova, Italy.
  • Cazzagon N; University of Padova, Padova, Italy.
  • Russo FP; University of Padova, Padova, Italy.
  • Burra P; University of Padova, Padova, Italy.
  • Zigmound U; Tel Aviv Medical Centre, Tel Aviv, Israel.
  • Houri I; Tel Aviv Medical Centre, Tel Aviv, Israel.
  • Carbone M; University of Milano-Bicocca, Milan, Italy.
  • Mulinacci G; University of Milano-Bicocca, Milan, Italy.
  • Fagiuoli S; Gastroenterology Hepatology and Transplantation UNIT, ASST Papa Giovanni XXIII, Bergamo & Department of Medicine, University of Milano-Bicocca, Milan, Italy.
  • Pratt DS; Massachusetts General Hospital, Harvard Medical School, Boston, USA.
  • Bonder A; Liver Center, Beth Israel Deaconess Medical Center, Department of Internal Medicine, Harvard Medical School, Boston, MA, USA.
  • Schiano TD; Mount Sinai Medical Center, New York, USA.
  • Haydel B; Mount Sinai Medical Center, New York, USA.
  • Lohse A; University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Schramm C; Martin Zeitz Center for Rare Diseases, University Medical Center Hamburg-Eppendorf, Germany.
  • Rüther D; University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Casu S; INSELSPITAL, Universitätsspital Bern, Switzerland.
  • Verhelst X; Ghent University Hospital, Ghent, Belgium.
  • Beretta-Piccoli BT; Epatocentro Ticino, Lugano, Switzerland.
J Hepatol ; 2024 May 29.
Article em En | MEDLINE | ID: mdl-38821360
ABSTRACT
BACKGROUND &

AIMS:

Recurrent primary biliary cholangitis (rPBC) develops in approximately 30% of patients and negatively impacts graft and overall patient survival after liver transplantation (LT). There is a lack of data regarding the response rate to ursodeoxycholic acid (UDCA) in rPBC. We evaluated a large, international, multi-center cohort to assess the performance of PBC scores in predicting the risk of graft and overall survival after LT in patients with rPBC.

METHODS:

A total of 332 patients with rPBC after LT were evaluated from 28 centers across Europe, North and South America. The median age at the time of rPBC was 58.0 years [IQR 53.2-62.6], and 298 patients (90%) were female. The biochemical response was measured with serum levels of alkaline phosphatase (ALP) and bilirubin, and Paris-2, GLOBE and UK-PBC scores at 1 year after UDCA initiation.

RESULTS:

During a median follow-up of 8.7 years [IQR 4.3-12.9] after rPBC diagnosis, 52 patients (16%) had graft loss and 103 (31%) died. After 1 year of UDCA initiation the histological stage at rPBC (hazard ratio [HR] 3.97, 95% CI 1.36-11.55, p = 0.01), use of prednisone (HR 3.18, 95% CI 1.04-9.73, p = 0.04), ALP xULN (HR 1.59, 95% CI 1.26-2.01, p <0.001), Paris-2 criteria (HR 4.14, 95% CI 1.57-10.92, p = 0.004), GLOBE score (HR 2.82, 95% CI 1.71-4.66, p <0.001), and the UK-PBC score (HR 1.06, 95% CI 1.03-1.09, p <0.001) were associated with graft survival in the multivariate analysis. Similar results were observed for overall survival.

CONCLUSION:

Patients with rPBC and disease activity, as indicated by standard PBC risk scores, have impaired outcomes, supporting efforts to treat recurrent disease in similar ways to pre-transplant PBC. IMPACT AND IMPLICATIONS One in three people who undergo liver transplantation for primary biliary cholangitis develop recurrent disease in their new liver. Patients with recurrent primary biliary cholangitis and incomplete response to ursodeoxycholic acid, according to conventional prognostic scores, have worse clinical outcomes, with higher risk of graft loss and mortality in similar ways to the disease before liver transplantation. Our results supportsupport efforts to treat recurrent disease in similar ways to pre-transplant primary biliary cholangitis.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Hepatol Assunto da revista: GASTROENTEROLOGIA Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Hepatol Assunto da revista: GASTROENTEROLOGIA Ano de publicação: 2024 Tipo de documento: Article