Alvarado-Tapias Edilmar, Pose Elisa, Gratacós-Ginès Jordi, Clemente-Sánchez Ana, López-Pelayo Hugo, Bataller Ramón
Department of Gastroenterology and Hepatology, Hospital of Santa Creu and Sant Pau, Autonomus University of Barcelona, Barcelona, Spain.
Centre for Biomedical Research in Liver and Digestive Diseases Network (CIBERehd), Madrid, Spain.
Clin Mol Hepatol. 2025 Feb;31(Suppl):S112-S133. doi: 10.3350/cmh.2024.0709. Epub 2024 Oct 31.
Alcohol consumption is a leading cause of preventable morbidity and mortality worldwide and the primary cause of advanced liver disease. Alcohol use disorder is a chronic, frequently relapsing condition characterized by persistent alcohol consumption despite its negative consequences. Alcohol-associated liver disease (ALD) encompasses a series of stages, from fatty liver (steatosis) to inflammation (steatohepatitis), fibrosis, and, ultimately, liver cirrhosis and its complications. The development of ALD is complex, involving both genetic and environmental factors, yet the exact mechanisms at play remain unclear. Alcohol-associated hepatitis (AH), a severe form of ALD, presents with sudden jaundice and liver failure. Currently, there are no approved targeted therapies able to interfere in the pathogenesis of ALD to stop the progression of the disease, making alcohol abstinence the most effective way to improve prognosis across all stages of ALD. For patients with advanced ALD who do not respond to medical therapy, liver transplantation is the only option that can improve prognosis. Recently, AH has become an early indication for liver transplantation in non-responders to medical treatment, showing promising results in carefully selected patients. This review provides an update on the epidemiology, natural history, pathogenesis, and current treatments for ALD. A deeper insight into novel targeted therapies investigated for AH focusing on new pathophysiologically-based agents is also discussed, including anti-inflammatory and antioxidative stress drugs, gut-liver axis modulators, and hepatocyte regenerative molecules.
饮酒是全球可预防发病和死亡的主要原因,也是晚期肝病的主要病因。酒精使用障碍是一种慢性、经常复发的疾病,其特征是尽管有负面后果仍持续饮酒。酒精性肝病(ALD)包括一系列阶段,从脂肪肝(脂肪变性)到炎症(脂肪性肝炎)、纤维化,最终发展为肝硬化及其并发症。ALD的发展很复杂,涉及遗传和环境因素,但具体的发病机制仍不清楚。酒精性肝炎(AH)是ALD的一种严重形式,表现为突然出现黄疸和肝功能衰竭。目前,尚无获批的能够干预ALD发病机制以阻止疾病进展的靶向治疗方法,戒酒是改善ALD各阶段预后的最有效方法。对于对药物治疗无反应的晚期ALD患者,肝移植是唯一能改善预后的选择。最近,AH已成为药物治疗无反应者肝移植的早期指征,在精心挑选的患者中显示出有希望的结果。本综述提供了ALD的流行病学、自然史、发病机制和当前治疗方法的最新信息。还讨论了针对AH研究的新型靶向治疗方法的更深入见解,重点是基于新病理生理学的药物,包括抗炎和抗氧化应激药物、肠-肝轴调节剂和肝细胞再生分子。