Yamazaki Tomoo, Schnabl Bernd
Department of Medicine, University of California San Diego, California, La Jolla, USA.
Department of Medicine, Division of Gastroenterology and Hepatology, Shinshu University School of Medicine, Nagano, Matsumoto, Japan.
Liver Int. 2025 Mar;45(3):e15608. doi: 10.1111/liv.15608. Epub 2023 May 15.
Acute alcohol-associated hepatitis (AH) is a syndrome that occurs in heavy and long-term drinkers and results in severe jaundice and liver failure. The mortality rate in severe cases is 20%-50% at 28 days, and in cases that do not improve despite appropriately timed corticosteroid therapy, the mortality rate reaches 70% at 6 months. The only curative treatment is early liver transplantation, but less than 2% of patients with severe AH are eligible. In order to improve the prognosis, diagnostic tools are needed to detect appropriate cases at risk of severe conditions, and new therapies need to be developed that can replace corticosteroids. Recent research has revealed that the pathogenesis of AH involves a complex of factors, including changes in the gut microbiota, inflammatory and cytokine signalling, oxidative stress and mitochondrial dysfunction, and abnormalities in the hepatic regenerative capacity. Non-invasive diagnostic tools focusing on these specific pathologies have been reported in recent years. In addition, several novel agents targeting specific pathways are currently being developed and tested in clinical trials. This review will provide an overview of alcohol-associated hepatitis and focus on the latest diagnostic tools, particularly non-invasive biomarkers, and novel therapies.
急性酒精性肝炎(AH)是一种发生于长期大量饮酒者的综合征,可导致严重黄疸和肝衰竭。严重病例在28天时的死亡率为20% - 50%,而即便接受了适时的皮质类固醇治疗仍无改善的病例,6个月时的死亡率可达70%。唯一的治愈性治疗方法是早期肝移植,但只有不到2%的重症AH患者符合条件。为改善预后,需要有诊断工具来检测有发生严重病情风险的合适病例,并且需要开发能够替代皮质类固醇的新疗法。最近的研究表明,AH的发病机制涉及多种因素,包括肠道微生物群的变化、炎症和细胞因子信号传导、氧化应激和线粒体功能障碍,以及肝脏再生能力异常。近年来已有针对这些特定病理情况的非侵入性诊断工具的报道。此外,目前有几种针对特定途径的新型药物正在进行临床试验开发和测试。本综述将概述酒精性肝炎,并重点介绍最新的诊断工具,特别是非侵入性生物标志物和新型疗法。