Current and emerging therapies for alcohol-associated hepatitis

Q2 Medicine
Francisco Idalsoaga , Gustavo Ayares , Luis Antonio Díaz , Jorge Arnold , María Ayala-Valverde , David Hudson , Marco Arrese , Juan Pablo Arab
{"title":"Current and emerging therapies for alcohol-associated hepatitis","authors":"Francisco Idalsoaga ,&nbsp;Gustavo Ayares ,&nbsp;Luis Antonio Díaz ,&nbsp;Jorge Arnold ,&nbsp;María Ayala-Valverde ,&nbsp;David Hudson ,&nbsp;Marco Arrese ,&nbsp;Juan Pablo Arab","doi":"10.1016/j.livres.2023.03.002","DOIUrl":null,"url":null,"abstract":"<div><p>Alcohol-related liver disease (ALD) encompasses a spectrum of diseases caused by excessive alcohol consumption. ALD includes hepatic steatosis, steatohepatitis, variable degrees of fibrosis, cirrhosis, and alcohol-associated hepatitis (AH), the latter being the most severe acute form of the disease. Severe AH is associated with high mortality (reaching up to 30%–50%) at 90 days. The cornerstone of ALD, and particularly AH, treatment continues to be abstinence, accompanied by support measures such as nutritional supplementation and management of alcohol withdrawal syndrome (AWS). In severe AH with model for end-stage liver disease (MELD) score ≥21, corticosteroids can be used, especially MELD score between 25 and 39, where the highest benefit is achieved. Other key aspects of treatment include the early identification of infections and their associated management and the proper identification of potential candidates for liver transplantation. The development of new therapies based on the pathophysiology and mechanisms of liver injury are underway. This includes the modulation and management of the innate immune response, gut dysbiosis, bacterial translocation, and bacteria-derived products from the intestine. These hold promise for the future of AH treatment.</p></div>","PeriodicalId":36741,"journal":{"name":"Liver Research","volume":"7 1","pages":"Pages 35-46"},"PeriodicalIF":0.0000,"publicationDate":"2023-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Liver Research","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2542568423000077","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 1

Abstract

Alcohol-related liver disease (ALD) encompasses a spectrum of diseases caused by excessive alcohol consumption. ALD includes hepatic steatosis, steatohepatitis, variable degrees of fibrosis, cirrhosis, and alcohol-associated hepatitis (AH), the latter being the most severe acute form of the disease. Severe AH is associated with high mortality (reaching up to 30%–50%) at 90 days. The cornerstone of ALD, and particularly AH, treatment continues to be abstinence, accompanied by support measures such as nutritional supplementation and management of alcohol withdrawal syndrome (AWS). In severe AH with model for end-stage liver disease (MELD) score ≥21, corticosteroids can be used, especially MELD score between 25 and 39, where the highest benefit is achieved. Other key aspects of treatment include the early identification of infections and their associated management and the proper identification of potential candidates for liver transplantation. The development of new therapies based on the pathophysiology and mechanisms of liver injury are underway. This includes the modulation and management of the innate immune response, gut dysbiosis, bacterial translocation, and bacteria-derived products from the intestine. These hold promise for the future of AH treatment.

酒精相关性肝炎的当前和新兴疗法
酒精相关性肝病(ALD)包括一系列由过量饮酒引起的疾病。ALD包括肝脂肪变性、脂肪性肝炎、不同程度纤维化、肝硬化和酒精相关性肝炎(AH),后者是该疾病最严重的急性形式。严重的AH与90天内的高死亡率(高达30%-50%)相关。ALD,特别是AH,治疗的基础仍然是戒酒,并辅以营养补充和酒精戒断综合征(AWS)管理等支持措施。对于终末期肝病模型(MELD)评分≥21的严重AH,可以使用皮质类固醇,尤其是MELD评分在25 - 39之间,获益最大。治疗的其他关键方面包括早期识别感染及其相关管理,以及正确识别肝移植的潜在候选者。基于肝损伤病理生理学和机制的新疗法正在发展中。这包括先天免疫反应的调节和管理、肠道生态失调、细菌易位和肠道细菌衍生产物。这些都为AH治疗的未来带来了希望。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Liver Research
Liver Research Medicine-Gastroenterology
CiteScore
5.90
自引率
0.00%
发文量
27
审稿时长
13 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信