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肝硬化再代偿的机制及意义

Mechanisms and implications of recompensation in cirrhosis.

作者信息

Piano Salvatore, Reiberger Thomas, Bosch Jaime

机构信息

Unit of Internal Medicine and Hepatology, Department of Medicine - DIMED, University and Hospital of Padova, Italy.

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

出版信息

JHEP Rep. 2024 Oct 10;6(12):101233. doi: 10.1016/j.jhepr.2024.101233. eCollection 2024 Dec.

Abstract

Decompensated cirrhosis has long been considered the irreversible end stage of liver disease, characterised by further decompensating events until death or liver transplantation. However, the observed clinical improvements after effective antiviral treatments for HBV and HCV and after sustained alcohol abstinence have changed this paradigm, leading to the concept of "recompensation" of cirrhosis. Recompensation of cirrhosis was recently defined by Baveno VII as (i) cure of the primary liver disease aetiology; (ii) disappearance of signs of decompensation (ascites, encephalopathy and portal hypertensive bleeding) off therapy; and (iii) stable improvement of liver function tests (bilirubin, international normalised ratio and albumin). Achieving these recompensation criteria is linked to a significant survival benefit. However, apart from aetiological therapies, no interventions/treatments that facilitate recompensation are available, the molecular mechanisms underlying recompensation remain incompletely understood, and early predictors of recompensation are lacking. Moreover, current recompensation criteria are based on expert opinion and may be refined in the future. Herein, we review the available evidence on cirrhosis recompensation, provide guidance on the clinical management of recompensated patients and discuss future challenges related to cirrhosis recompensation.

摘要

失代偿期肝硬化长期以来一直被视为肝病的不可逆终末期,其特征是出现进一步的失代偿事件,直至死亡或进行肝移植。然而,针对乙肝病毒(HBV)和丙肝病毒(HCV)的有效抗病毒治疗以及持续戒酒之后观察到的临床改善改变了这一模式,从而引出了肝硬化“再代偿”的概念。最近,巴韦诺第七届共识会议将肝硬化再代偿定义为:(i)原发性肝病病因得到治愈;(ii)停止治疗后失代偿体征(腹水、肝性脑病和门静脉高压出血)消失;(iii)肝功能检查(胆红素、国际标准化比值和白蛋白)持续改善。达到这些再代偿标准与显著的生存获益相关。然而,除了病因治疗外,尚无促进再代偿的干预措施/治疗方法,再代偿的分子机制仍未完全明确,且缺乏再代偿的早期预测指标。此外,目前的再代偿标准基于专家意见,未来可能会进一步完善。在此,我们综述了有关肝硬化再代偿的现有证据,为再代偿患者的临床管理提供指导,并讨论与肝硬化再代偿相关的未来挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7373/11617229/6cb721c9fab6/gr1.jpg

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