Hepatic venous pressure gradient predicts risk of hepatic decompensation and liver-related mortality in patients with MASLD.

MASLD advanced chronic liver disease hepatic decompensation hepatic venous pressure gradient portal hypertension

Journal

Journal of hepatology
ISSN: 1600-0641
Titre abrégé: J Hepatol
Pays: Netherlands
ID NLM: 8503886

Informations de publication

Date de publication:
30 May 2024
Historique:
received: 07 12 2023
revised: 02 05 2024
accepted: 22 05 2024
medline: 2 6 2024
pubmed: 2 6 2024
entrez: 1 6 2024
Statut: aheadofprint

Résumé

Metabolic dysfunction-associated steatotic liver disease (MASLD) is a leading cause of advanced chronic liver disease (ACLD). Portal hypertension drives hepatic decompensation and is best diagnosed by hepatic venous pressure gradient (HVPG) measurement. Here we investigate the prognostic value of HVPG in compensated (cACLD) MASLD. This European multicentre study included MASLD-cACLD patients characterised by HVPG at baseline. Hepatic decompensation (variceal bleeding/ ascites/hepatic encephalopathy) and liver-related mortality were considered the primary events of interest. 340 MASLD-cACLD patients [56.2% men; age: 62 (55-68) years; MELD: 8 (7-9); 71.2% diabetes] were included. Clinically significant portal hypertension (CSPH; i.e., HVPG ≥10 mmHg) was found in 209 patients (61.5%). During a median follow-up of 41.5 (27.5-65.8) months, 65 patients developed hepatic decompensation with a cumulative incidence of 10.0% after 2 years (2Y) and 30.7% after 5 years (5Y) in MASLD-cACLD with CSPH, compared to 2.4% after 2Y and 9.4% after 5Y in patients without CSPH. Variceal bleeding did not occur without CSPH. CSPH (subdistribution hazard ratio, SHR:5.13; p<0.001) was associated with an increased decompensation risk and a higher HVPG remained an independent risk factor in the multivariable model (aSHR per mmHg:1.12; p<0.001). Liver-related mortality occurred in 37 patients with a cumulative incidence of 3.3% after 2Y and 21.4% after 5Y in CSPH. Without CSPH, the incidence after 5Y was 0.8%. Accordingly, a higher HVPG was also independently associated with a higher risk of liver-related death (aSHR per mmHg:1.20; p<0.001). HVPG measurement is of high prognostic value in MASLD-cACLD. While MASLD-cACLD patients without CSPH show a very low short-term risk of decompensation and liver-related mortality is rare, the presence of CSPH substantially increases both risks. While the incidence of compensated advanced chronic liver disease (cACLD) due to metabolic dysfunction-associated steatotic liver disease (MASLD) is increasing worldwide, insights into the impact of clinically significant portal hypertension (CSPH) on the risk of liver-related events in MASLD-cACLD remain limited. Based on the findings of this European multicentre study including 340 MASLD-cACLD, we could show that increasing HVPG values and the presence of CSPH in particular were associated with a significantly higher risk of first hepatic decompensation and liver-related mortality. In contrast, the short-term incidence of decompensation in MASLD-cACLD patients without CSPH was low and the risk of liver-mortality remained negligible. Thus, HVPG measurements can provide important prognostic information for individualised risk-stratification in MASLD-cACLD and may help facilitate the study of novel and promising treatment possibilities for MASLD.

Sections du résumé

BACKGROUND & AIMS OBJECTIVE
Metabolic dysfunction-associated steatotic liver disease (MASLD) is a leading cause of advanced chronic liver disease (ACLD). Portal hypertension drives hepatic decompensation and is best diagnosed by hepatic venous pressure gradient (HVPG) measurement. Here we investigate the prognostic value of HVPG in compensated (cACLD) MASLD.
METHODS METHODS
This European multicentre study included MASLD-cACLD patients characterised by HVPG at baseline. Hepatic decompensation (variceal bleeding/ ascites/hepatic encephalopathy) and liver-related mortality were considered the primary events of interest.
RESULTS RESULTS
340 MASLD-cACLD patients [56.2% men; age: 62 (55-68) years; MELD: 8 (7-9); 71.2% diabetes] were included. Clinically significant portal hypertension (CSPH; i.e., HVPG ≥10 mmHg) was found in 209 patients (61.5%). During a median follow-up of 41.5 (27.5-65.8) months, 65 patients developed hepatic decompensation with a cumulative incidence of 10.0% after 2 years (2Y) and 30.7% after 5 years (5Y) in MASLD-cACLD with CSPH, compared to 2.4% after 2Y and 9.4% after 5Y in patients without CSPH. Variceal bleeding did not occur without CSPH. CSPH (subdistribution hazard ratio, SHR:5.13; p<0.001) was associated with an increased decompensation risk and a higher HVPG remained an independent risk factor in the multivariable model (aSHR per mmHg:1.12; p<0.001). Liver-related mortality occurred in 37 patients with a cumulative incidence of 3.3% after 2Y and 21.4% after 5Y in CSPH. Without CSPH, the incidence after 5Y was 0.8%. Accordingly, a higher HVPG was also independently associated with a higher risk of liver-related death (aSHR per mmHg:1.20; p<0.001).
CONCLUSION CONCLUSIONS
HVPG measurement is of high prognostic value in MASLD-cACLD. While MASLD-cACLD patients without CSPH show a very low short-term risk of decompensation and liver-related mortality is rare, the presence of CSPH substantially increases both risks.
IMPACT AND IMPLICATIONS UNASSIGNED
While the incidence of compensated advanced chronic liver disease (cACLD) due to metabolic dysfunction-associated steatotic liver disease (MASLD) is increasing worldwide, insights into the impact of clinically significant portal hypertension (CSPH) on the risk of liver-related events in MASLD-cACLD remain limited. Based on the findings of this European multicentre study including 340 MASLD-cACLD, we could show that increasing HVPG values and the presence of CSPH in particular were associated with a significantly higher risk of first hepatic decompensation and liver-related mortality. In contrast, the short-term incidence of decompensation in MASLD-cACLD patients without CSPH was low and the risk of liver-mortality remained negligible. Thus, HVPG measurements can provide important prognostic information for individualised risk-stratification in MASLD-cACLD and may help facilitate the study of novel and promising treatment possibilities for MASLD.

Identifiants

pubmed: 38823501
pii: S0168-8278(24)00368-4
doi: 10.1016/j.jhep.2024.05.033
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024. Published by Elsevier B.V.

Auteurs

Rafael Paternostro (R)

Division of Gastroenterology and Hepatology, Department of Medicine III, Medical University of Vienna, Vienna, Austria.

Wilhelmus J Kwanten (WJ)

Department of Gastroenterology and Hepatology, Antwerp University Hospital, Edegem, Belgium; Laboratory of Experimental Medicine and Pediatrics (LEMP), Division of Gastroenterology-Hepatology, Faculty of Medicine and Health Sciences, University of Antwerp, Antwerp, Belgium.

Benedikt Silvester Hofer (BS)

Division of Gastroenterology and Hepatology, Department of Medicine III, Medical University of Vienna, Vienna, Austria.

Georg Semmler (G)

Division of Gastroenterology and Hepatology, Department of Medicine III, Medical University of Vienna, Vienna, Austria.

Ali Bagdadi (A)

Department of Gastroenterology and Hepatology, Antwerp University Hospital, Edegem, Belgium.

Irina Luzko (I)

Liver Unit, Hospital Clinic, IDIBAPS, University of Barcelona, Spain.

Virginia Hernández-Gea (V)

Liver Unit, Hospital Clinic, IDIBAPS, University of Barcelona, Spain.

Isabel Graupera (I)

Liver Unit, Hospital Clinic, IDIBAPS, University of Barcelona, Spain.

Juan Carlos García-Pagán (JC)

Liver Unit, Hospital Clinic, IDIBAPS, University of Barcelona, Spain.

Dario Saltini (D)

Division of Gastroenterology, Azienda Ospedaliero-Universitaria di Modena and University of Modena and Reggio emilia, Modena, Italy.

Federica Indulti (F)

Division of Gastroenterology, Azienda Ospedaliero-Universitaria di Modena and University of Modena and Reggio emilia, Modena, Italy.

Filippo Schepis (F)

Division of Gastroenterology, Azienda Ospedaliero-Universitaria di Modena and University of Modena and Reggio emilia, Modena, Italy.

Lucile Moga (L)

Service d'Hépatologie, AP-HP, Hôpital Beaujon, DMU DIGEST, Centre de Référence des Maladies Vasculaires du Foie, FILFOIE, Clichy, France.

Pierre-Emanuel Rautou (PE)

Service d'Hépatologie, AP-HP, Hôpital Beaujon, DMU DIGEST, Centre de Référence des Maladies Vasculaires du Foie, FILFOIE, Clichy, France.

Elba Llop (E)

Liver unit, Hospital U, Puerta de Hierro. Universidad Autònoma de Madrid, CIBERehd, Madrid, Spain.

Luis Téllez (L)

Department of Gastroenterology, Hospital Universitario Ramón y Cajal. Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS), Universidad de Alcalá, Madrid, Spain.

Agustín Albillos (A)

Department of Gastroenterology, Hospital Universitario Ramón y Cajal. Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS), Universidad de Alcalá, Madrid, Spain.

Jose Ignacio Fortea (JI)

Gastroenterology and Hepatology Department, University Hospital Marqués de Valdecilla, Health Research Institute Marqués de Valdecilla (IDIVAL), Santander, Spain.

Angela Puente (A)

Gastroenterology and Hepatology Department, University Hospital Marqués de Valdecilla, Health Research Institute Marqués de Valdecilla (IDIVAL), Santander, Spain.

Giulia Tosetti (G)

Division of Gastroenterology and Hepatology, Fundation IRCCS CáGranda Ospedale Maggiore Policlinico, University of Milan, Milan, Italy.

Massimo Primignani (M)

Division of Gastroenterology and Hepatology, Fundation IRCCS CáGranda Ospedale Maggiore Policlinico, University of Milan, Milan, Italy.

Alexander Zipprich (A)

First Department of Internal Medicine, Martin Luther University Halle-Wittenberg, Halle (Saale), Germany; Department of Internal Medicine IV, Jena University Hospital, Friedrich-Schiller University Jena.

Elise Vuille-Lessard (E)

Hepatology, Inselspital, University Clinic of Visceral Surgery and Medicine (UVCM), University of Bern, Switzerland.

Annalisa Berzigotti (A)

Hepatology, Inselspital, University Clinic of Visceral Surgery and Medicine (UVCM), University of Bern, Switzerland.

Madalina-Gabriela Taru (MG)

Regional Institute of Gastroenterology and Hepatology "Octavian fodor", Hepatology Department and "luliu Hatieganu" University of medicine and Pharmacy, 3rd Medical Clinic, Cluj-Napoca, Romania.

Vlad Taru (V)

Regional Institute of Gastroenterology and Hepatology "Octavian fodor", Hepatology Department and "luliu Hatieganu" University of medicine and Pharmacy, 3rd Medical Clinic, Cluj-Napoca, Romania.

Bogdan Procopet (B)

Regional Institute of Gastroenterology and Hepatology "Octavian fodor", Hepatology Department and "luliu Hatieganu" University of medicine and Pharmacy, 3rd Medical Clinic, Cluj-Napoca, Romania.

Christian Jansen (C)

Department of Internal Medicine I, University Hospital Bonn, Venusberg-Campus 1, 53127 Bonn, Germany.

Michael Praktiknjo (M)

Department of Internal Medicine B, University Hospital of Münster, Münster, Germany.

Wenyi Gu (W)

Department of Internal Medicine B, University Hospital of Münster, Münster, Germany.

Jonel Trebicka (J)

Department of Internal Medicine B, University Hospital of Münster, Münster, Germany.

Luis Ibanez-Samaniego (L)

Servicio de Medicina del Aparato Digestivo. IiSGM. Hospital General Universitario Gregorio Marañón. Facultad de Medicina. Universidad Complutense. CIBERehd. Madrid. Spain.

Rafael Bañares (R)

Servicio de Medicina del Aparato Digestivo. IiSGM. Hospital General Universitario Gregorio Marañón. Facultad de Medicina. Universidad Complutense. CIBERehd. Madrid. Spain.

Jesús Rivera-Esteban (J)

Liver Unit, Vall d'Hebron University Hospital, Vall d'Hebron Institut of Research (VHIR), Vall d'Hebron Barcelona Hospital Campus, Autonomous University of Barcelona,Barcelona; CIBEREHD, Madrid, Spain.

Juan M Pericas (JM)

Liver Unit, Vall d'Hebron University Hospital, Vall d'Hebron Institut of Research (VHIR), Vall d'Hebron Barcelona Hospital Campus, Autonomous University of Barcelona,Barcelona; CIBEREHD, Madrid, Spain.

Joan Genesca (J)

Liver Unit, Vall d'Hebron University Hospital, Vall d'Hebron Institut of Research (VHIR), Vall d'Hebron Barcelona Hospital Campus, Autonomous University of Barcelona,Barcelona; CIBEREHD, Madrid, Spain.

Edilmar Alvarado (E)

Servei de Patología Digestiva, Hospital de la Santa Creu i Sant Pau, Barcelona Spain; Universitat autònoma de Barcelona, Bellaterra, Barcelona, Spain.

Candid Villanueva (C)

Servei de Patología Digestiva, Hospital de la Santa Creu i Sant Pau, Barcelona Spain; Universitat autònoma de Barcelona, Bellaterra, Barcelona, Spain.

Helene Larrue (H)

Department of Hepato-gastroenterology, Purpan Hospital, CHU Toulouse, InSERM U858, University of Toulouse, Université Paul Sabatier Touluse, France.

Christophe Bureau (C)

Department of Hepato-gastroenterology, Purpan Hospital, CHU Toulouse, InSERM U858, University of Toulouse, Université Paul Sabatier Touluse, France.

Wim Laleman (W)

Department of Gastroenterology and Hepatology, University Hospitals Leuven, Leuven, Belgium.

Alba Ardevol (A)

Hospital Universitari Germans Trias I Pujol, Universitat Autònoma de Barcelona, Badalona, Spain.

Helena Masnou (H)

Hospital Universitari Germans Trias I Pujol, Universitat Autònoma de Barcelona, Badalona, Spain.

Thomas Vanwolleghem (T)

Department of Gastroenterology and Hepatology, Antwerp University Hospital, Edegem, Belgium.

Michael Trauner (M)

Division of Gastroenterology and Hepatology, Department of Medicine III, Medical University of Vienna, Vienna, Austria.

Mattias Mandorfer (M)

Division of Gastroenterology and Hepatology, Department of Medicine III, Medical University of Vienna, Vienna, Austria.

Sven Francque (S)

Department of Gastroenterology and Hepatology, Antwerp University Hospital, Edegem, Belgium; Laboratory of Experimental Medicine and Pediatrics (LEMP), Division of Gastroenterology-Hepatology, Faculty of Medicine and Health Sciences, University of Antwerp, Antwerp, Belgium.

Thomas Reiberger (T)

Division of Gastroenterology and Hepatology, Department of Medicine III, Medical University of Vienna, Vienna, Austria. Electronic address: thomas.reiberger@meduniwien.ac.at.

Classifications MeSH