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

门静脉压 医学 失代偿 门脉高压 内科学 胃肠病学 肝病 慢性肝病 肝硬化 心脏病学
作者
Rafael Paternostro,Wilhelmus J. Kwanten,Benedikt Hofer,Georg Semmler,Ali Bagdadi,Irina Luzko,Jaume Bosch,Isabel Graupera,Juan Carlos García–Pagán,Dario Saltini,Federica Indulti,Filippo Schepis,Lucile Moga,Pierre‐Emmanuel Rautou,Elba Llop,Luís Téllez,Agustı́n Albillos,José Ignacio Fortea,Ángela Puente,Giulia Tosetti,Massimo Primignani,Alexander Zipprich,Élise Vuille‐Lessard,Annalisa Berzigotti,Mădălina-Gabriela Țâru,Vlad Țâru,Bogdan Procopeţ,Christian Jansen,Michael Praktiknjo,Wenyu Gu,Jonel Trebicka,Luis Ibáñez,Rafael Bañares,Jesús Rivera‐Esteban,Juan M. Pericàs,Joan Genescà,Edilmar Alvarado‐Tápias,Càndid Villanueva,Hélène Larrue,Christophe Bureau,Wim Laleman,Alba Ardèvol,Helena Masnou,Thomas Vanwolleghem,Michael Trauner,Mattias Mandorfer,Sven Francque,Thomas Reiberger
出处
期刊:Journal of Hepatology [Elsevier]
被引量:2
标识
DOI:10.1016/j.jhep.2024.05.033
摘要

Background & AimsMetabolic 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.MethodsThis 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.Results340 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).ConclusionHVPG 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 IMPLICATIONSWhile 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.
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