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Adequate versus deep response to ursodeoxycholic acid in primary biliary cholangitis: To what extent and under what conditions is normal alkaline phosphatase level associated with complication-free survival gain?
Corpechot, Christophe; Lemoinne, Sara; Soret, Pierre-Antoine; Hansen, Bettina; Hirschfield, Gideon; Gulamhusein, Aliya; Montano-Loza, Aldo J; Lytvyak, Ellina; Pares, Albert; Olivas, Ignasi; Eaton, John E; Osman, Karim T; Schramm, Christoph; Sebode, Marcial; Lohse, Ansgar W; Dalekos, George; Gatselis, Nikolaos; Nevens, Frederik; Cazzagon, Nora; Zago, Alessandra; Russo, Francesco Paolo; Floreani, Annarosa; Abbas, Nadir; Trivedi, Palak; Thorburn, Douglas; Saffioti, Francesca; Barkai, Laszlo; Roccarina, Davide; Calvaruso, Vicenza; Fichera, Anna; Delamarre, Adèle; Sobenko, Natalia; Villamil, Alejandra Maria; Medina-Morales, Esli; Bonder, Alan; Patwardhan, Vilas; Rigamonti, Cristina; Carbone, Marco; Invernizzi, Pietro; Cristoferi, Laura; van der Meer, Adriaan; de Veer, Rozanne; Zigmond, Ehud; Yehezkel, Eyal; Kremer, Andreas E; Deibel, Ansgar; Bruns, Tony; Große, Karsten; Wetten, Aaron; Dyson, Jessica Katharine.
Afiliación
  • Corpechot C; Reference Center for Inflammatory Biliary Diseases and Autoimmune Hepatitis, European Reference Network on Hepatological Diseases (ERN Rare-Liver), Saint-Antoine Hospital, Assistance Publique-Hôpitaux de Paris; Inserm UMR_S938, Saint-Antoine Research Center, Sorbonne University, Paris, France.
  • Lemoinne S; Reference Center for Inflammatory Biliary Diseases and Autoimmune Hepatitis, European Reference Network on Hepatological Diseases (ERN Rare-Liver), Saint-Antoine Hospital, Assistance Publique-Hôpitaux de Paris; Inserm UMR_S938, Saint-Antoine Research Center, Sorbonne University, Paris, France.
  • Soret PA; Reference Center for Inflammatory Biliary Diseases and Autoimmune Hepatitis, European Reference Network on Hepatological Diseases (ERN Rare-Liver), Saint-Antoine Hospital, Assistance Publique-Hôpitaux de Paris; Inserm UMR_S938, Saint-Antoine Research Center, Sorbonne University, Paris, France.
  • Hansen B; Department of Epidemiology & Biostatistics, Erasmus MC, Rotterdam, The Netherlands.
  • Hirschfield G; Toronto Centre for Liver Disease, University Health Network, University of Toronto, Toronto, Ontario, Canada.
  • Gulamhusein A; Toronto Centre for Liver Disease, University Health Network, University of Toronto, Toronto, Ontario, Canada.
  • Montano-Loza AJ; Toronto Centre for Liver Disease, University Health Network, University of Toronto, Toronto, Ontario, Canada.
  • Lytvyak E; Division of Gastroenterology and Liver Unit, University of Alberta, Edmonton, Alberta, Canada.
  • Pares A; Division of Preventive Medicine, University of Alberta, Edmonton, Alberta, Canada.
  • Olivas I; Liver Unit, Hospital Clínic, University of Barcelona, The August Pi i Sunyer Biomedical Research Institute, Biomedical Research Networking Center in Hepatic and Digestive Diseases, European Reference Network on Hepatological Diseases (ERN Rare-Liver), Barcelona, Spain.
  • Eaton JE; Liver Unit, Hospital Clínic, University of Barcelona, The August Pi i Sunyer Biomedical Research Institute, Biomedical Research Networking Center in Hepatic and Digestive Diseases, European Reference Network on Hepatological Diseases (ERN Rare-Liver), Barcelona, Spain.
  • Osman KT; Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
  • Schramm C; Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
  • Sebode M; Department of Medicine I and Martin Zeitz Center for Rare Diseases, European Reference Network on Hepatological Diseases (ERN Rare-Liver), University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Lohse AW; Department of Medicine I and Martin Zeitz Center for Rare Diseases, European Reference Network on Hepatological Diseases (ERN Rare-Liver), University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Dalekos G; Department of Medicine I and Martin Zeitz Center for Rare Diseases, European Reference Network on Hepatological Diseases (ERN Rare-Liver), University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Gatselis N; Department of Medicine and Research Laboratory of Internal Medicine, National Expertise Center of Greece in Autoimmune Liver Diseases, European Reference Network on Hepatological Diseases (ERN Rare-Liver), General University Hospital, Larissa, Greece.
  • Nevens F; Department of Medicine and Research Laboratory of Internal Medicine, National Expertise Center of Greece in Autoimmune Liver Diseases, European Reference Network on Hepatological Diseases (ERN Rare-Liver), General University Hospital, Larissa, Greece.
  • Cazzagon N; Division of Hepatology and Liver Transplantation, European Reference Network on Hepatological Diseases (ERN Rare-Liver), University Hospitals KU, Leuven, Belgium.
  • Zago A; Department of Surgery, Oncology and Gastroenterology, European Reference Network on Hepatological Diseases (ERN Rare-Liver), University of Padova, Padova, Italy.
  • Russo FP; Department of Surgery, Oncology and Gastroenterology, European Reference Network on Hepatological Diseases (ERN Rare-Liver), University of Padova, Padova, Italy.
  • Floreani A; Department of Surgery, Oncology and Gastroenterology, European Reference Network on Hepatological Diseases (ERN Rare-Liver), University of Padova, Padova, Italy.
  • Abbas N; Department of Surgery, Oncology and Gastroenterology, European Reference Network on Hepatological Diseases (ERN Rare-Liver), University of Padova, Padova, Italy.
  • Trivedi P; Liver Unit, University Hospitals Birmingham National Health Service Foundation Trust Queen Elizabeth, Birmingham, UK.
  • Thorburn D; National Institute for Health Research (NIHR) Birmingham Biomedical Research Centre (BRC), Institute of Immunology and Immunotherapy, Centre for Liver and Gastrointestinal Research, University of Birmingham, Birmingham, UK.
  • Saffioti F; University College London Institute for Liver and Digestive Health, Royal Free Hospital, London, UK.
  • Barkai L; University College London Institute for Liver and Digestive Health, Royal Free Hospital, London, UK.
  • Roccarina D; University College London Institute for Liver and Digestive Health, Royal Free Hospital, London, UK.
  • Calvaruso V; University College London Institute for Liver and Digestive Health, Royal Free Hospital, London, UK.
  • Fichera A; Section of Gastroenterology and Hepatology, PROMISE, University of Palermo, Palermo, Italy.
  • Delamarre A; Section of Gastroenterology and Hepatology, PROMISE, University of Palermo, Palermo, Italy.
  • Sobenko N; Department of Hepatology, University Hospitals of Bordeaux, Pessac, France.
  • Villamil AM; Department of Hepatology & Liver Transplantation, Italian Hospital of Buenos Aires, Buenos Aires, Argentina.
  • Medina-Morales E; Department of Hepatology & Liver Transplantation, Italian Hospital of Buenos Aires, Buenos Aires, Argentina.
  • Bonder A; Department of Medicine, Division of Gastroenterology, Beth Israel Deaconess Medical Center, Boston, Massachusetts.
  • Patwardhan V; Department of Medicine, Division of Gastroenterology, Beth Israel Deaconess Medical Center, Boston, Massachusetts.
  • Rigamonti C; Department of Medicine, Division of Gastroenterology, Beth Israel Deaconess Medical Center, Boston, Massachusetts.
  • Carbone M; 9Department of Internal Medicine, Università del Piemonte Orientale, Novara, Italy.
  • Invernizzi P; Division of Gastroenterology, Center for Autoimmune Liver Diseases, Department of Medicine and Surgery, European Reference Network on Hepatological Diseases (ERN Rare-Liver), University of Milano-Bicocca, Monza, Italy.
  • Cristoferi L; Division of Gastroenterology, Center for Autoimmune Liver Diseases, Department of Medicine and Surgery, European Reference Network on Hepatological Diseases (ERN Rare-Liver), University of Milano-Bicocca, Monza, Italy.
  • van der Meer A; Division of Gastroenterology, Center for Autoimmune Liver Diseases, Department of Medicine and Surgery, European Reference Network on Hepatological Diseases (ERN Rare-Liver), University of Milano-Bicocca, Monza, Italy.
  • de Veer R; Department of Gastroenterology and Hepatology, Erasmus University Medical Center, Rotterdam, The Netherlands.
  • Zigmond E; Department of Gastroenterology and Hepatology, Erasmus University Medical Center, Rotterdam, The Netherlands.
  • Yehezkel E; The Research Center for Digestive Tract and Liver Diseases, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.
  • Kremer AE; The Research Center for Digestive Tract and Liver Diseases, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.
  • Deibel A; Department of Gastroenterology and Hepatology, University Hospital Zürich, Zürich, Switzerland.
  • Bruns T; Department of Gastroenterology and Hepatology, University Hospital Zürich, Zürich, Switzerland.
  • Große K; Department of Medicine III, University Hospital RWTH Aachen, European Reference Network on Hepatological Diseases (ERN Rare-Liver), Aachen, Germany.
  • Wetten A; Department of Medicine III, University Hospital RWTH Aachen, European Reference Network on Hepatological Diseases (ERN Rare-Liver), Aachen, Germany.
  • Dyson JK; Department of Hepatology and Liver Transplantation, Newcastle Upon Tyne Hospitals NHS Foundation Trust and Newcastle University, Newcastle Upon Tyne, UK.
Hepatology ; 79(1): 39-48, 2024 Jan 01.
Article en En | MEDLINE | ID: mdl-37399238
BACKGROUND AND AIMS: Normal alkaline phosphatase (ALP) levels in ursodeoxycholic acid (UDCA)-treated patients with primary biliary cholangitis (PBC) are associated with better long-term outcome. However, second-line therapies are currently recommended only when ALP levels remain above 1.5 times the upper limit of normal (×ULN) after 12-month UDCA. We assessed whether, in patients considered good responders to UDCA, normal ALP levels were associated with significant survival gains. APPROACH AND RESULTS: We performed a retrospective cohort study of 1047 patients with PBC who attained an adequate response to UDCA according to Paris-2 criteria. Time to liver-related complications, liver transplantation, or death was assessed using adjusted restricted mean survival time (RMST) analysis. The overall incidence rate of events was 17.0 (95% CI: 13.7-21.1) per 1000 out of 4763.2 patient-years. On the whole population, normal serum ALP values (but not normal gamma-glutamyl transpeptidase (GGT), alanine aminotransferase (ALT), or aspartate aminotransferase (AST); or total bilirubin < 0.6 ×ULN) were associated with a significant absolute complication-free survival gain at 10 years (mean 7.6 months, 95% CI: 2.7 - 12.6 mo.; p = 0.003). In subgroup analysis, this association was significant in patients with a liver stiffness measurement ≥ 10 kPa and/or age ≤ 62 years, with a 10-year absolute complication-free survival gain of 52.8 months (95% CI: 45.7-59.9, p < 0.001) when these 2 conditions were met. CONCLUSIONS: PBC patients with an adequate response to UDCA and persistent ALP elevation between 1.1 and 1.5 ×ULN, particularly those with advanced fibrosis and/or who are sufficiently young, remain at risk of poor outcome. Further therapeutic efforts should be considered for these patients.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Ácido Ursodesoxicólico / Cirrosis Hepática Biliar Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Humans / Middle aged Idioma: En Revista: Hepatology Año: 2024 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Ácido Ursodesoxicólico / Cirrosis Hepática Biliar Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Humans / Middle aged Idioma: En Revista: Hepatology Año: 2024 Tipo del documento: Article País de afiliación: Francia