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ALD 治疗的新兴靶点:来自 NASH 的经验。

Emerging targets for therapy in ALD: Lessons from NASH.

机构信息

Department of Internal Medicine, University of South Dakota Sanford School of Medicine, Sioux Falls, South Dakota, USA.

Division of Gastroenterology and Hepatology, Avera Transplant Institute, Sioux Falls, South Dakota, USA.

出版信息

Hepatology. 2024 Jul 1;80(1):223-237. doi: 10.1097/HEP.0000000000000381. Epub 2023 Mar 21.

Abstract

Alcohol-associated liver disease due to harmful alcohol use and NAFLD associated with metabolic syndrome are the 2 most common liver diseases worldwide. Control of respective risk factors is the cornerstone in the long-term management of these diseases. Furthermore, there are no effective therapies. Both diseases are characterized by metabolic derangements; thus, the focus of this review was to broaden our understanding of metabolic targets investigated in NAFLD, and how these can be applied to alcohol-associated liver disease. Conserved pathogenic pathways such as dysregulated lipid metabolism, cell death pathways including apoptosis and activation of innate immune cells, and stellate cells mediate both alcohol and NAFLDs, resulting in histological abnormalities of steatosis, inflammation, fibrosis, and cirrhosis. However, pathways such as gut microbiome changes, glucose metabolism and insulin resistance, inflammatory signaling, and microRNA abnormalities are distinct in these 2 diseases. In this review article, we describe conserved and distinct pathogenic pathways highlighting therapeutic targets that may be of potential in both diseases and those that are unique to each disease.

摘要

由于有害饮酒和与代谢综合征相关的非酒精性脂肪性肝病(NAFLD)导致的酒精相关性肝病是全球 2 种最常见的肝病。控制各自的风险因素是这些疾病长期管理的基石。此外,目前还没有有效的治疗方法。这两种疾病的特点都是代谢紊乱;因此,本综述的重点是扩大我们对 NAFLD 中研究的代谢靶点的理解,以及这些靶点如何应用于酒精相关性肝病。失调的脂质代谢、包括细胞凋亡和固有免疫细胞激活在内的细胞死亡途径以及星状细胞等保守的致病途径介导了酒精和非酒精性脂肪性肝病,导致脂肪变性、炎症、纤维化和肝硬化的组织学异常。然而,肠道微生物组变化、葡萄糖代谢和胰岛素抵抗、炎症信号和 microRNA 异常等途径在这两种疾病中是不同的。在这篇综述文章中,我们描述了保守和独特的致病途径,强调了可能对这两种疾病都有潜在作用的治疗靶点,以及每种疾病所特有的靶点。

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