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Emerging medical therapies for severe alcoholic hepatitis

Severe alcoholic hepatitis (AH) is an acute and often devastating form of alcohol-associated liver disease. Clinically, AH is characterized by elevated bilirubin, model for end stage liver disease scores >20, and nonspecific symptoms that are caused by underlying inflammation, hepatocyte injury,...

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Detalles Bibliográficos
Autores principales: Tornai, David, Szabo, Gyongyi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Association for the Study of the Liver 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7641578/
https://www.ncbi.nlm.nih.gov/pubmed/32981291
http://dx.doi.org/10.3350/cmh.2020.0145
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author Tornai, David
Szabo, Gyongyi
author_facet Tornai, David
Szabo, Gyongyi
author_sort Tornai, David
collection PubMed
description Severe alcoholic hepatitis (AH) is an acute and often devastating form of alcohol-associated liver disease. Clinically, AH is characterized by elevated bilirubin, model for end stage liver disease scores >20, and nonspecific symptoms that are caused by underlying inflammation, hepatocyte injury, and impaired intestinal barrier function. Compromised immune defense in AH contributes to infections, sepsis and organ failure. To date, corticosteroids are the only recommended treatment for severe AH, however it does not provide survival benefits beyond 1 month. Recent preclinical and early clinical studies in AH aided understanding of the disease and presented opportunities for new therapeutic options targeting inflammation, oxidative stress, liver regeneration and modification of intestinal microbiota. In this comprehensive review, we discuss promising preclinical results and ongoing clinical trials evaluating novel therapeutic agents for the treatment of severe AH.
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spelling pubmed-76415782020-11-13 Emerging medical therapies for severe alcoholic hepatitis Tornai, David Szabo, Gyongyi Clin Mol Hepatol Review Severe alcoholic hepatitis (AH) is an acute and often devastating form of alcohol-associated liver disease. Clinically, AH is characterized by elevated bilirubin, model for end stage liver disease scores >20, and nonspecific symptoms that are caused by underlying inflammation, hepatocyte injury, and impaired intestinal barrier function. Compromised immune defense in AH contributes to infections, sepsis and organ failure. To date, corticosteroids are the only recommended treatment for severe AH, however it does not provide survival benefits beyond 1 month. Recent preclinical and early clinical studies in AH aided understanding of the disease and presented opportunities for new therapeutic options targeting inflammation, oxidative stress, liver regeneration and modification of intestinal microbiota. In this comprehensive review, we discuss promising preclinical results and ongoing clinical trials evaluating novel therapeutic agents for the treatment of severe AH. The Korean Association for the Study of the Liver 2020-10 2020-09-28 /pmc/articles/PMC7641578/ /pubmed/32981291 http://dx.doi.org/10.3350/cmh.2020.0145 Text en Copyright © 2020 by The Korean Association for the Study of the Liver This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Tornai, David
Szabo, Gyongyi
Emerging medical therapies for severe alcoholic hepatitis
title Emerging medical therapies for severe alcoholic hepatitis
title_full Emerging medical therapies for severe alcoholic hepatitis
title_fullStr Emerging medical therapies for severe alcoholic hepatitis
title_full_unstemmed Emerging medical therapies for severe alcoholic hepatitis
title_short Emerging medical therapies for severe alcoholic hepatitis
title_sort emerging medical therapies for severe alcoholic hepatitis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7641578/
https://www.ncbi.nlm.nih.gov/pubmed/32981291
http://dx.doi.org/10.3350/cmh.2020.0145
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