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Pathophysiology and Management of Alcoholic Liver Disease: Update 2016

Alcoholic liver disease (ALD) is a leading cause of cirrhosis, liver cancer, and acute and chronic liver failure and as such causes significant morbidity and mortality. While alcohol consumption is slightly decreasing in several European countries, it is rising in others and remains high in many cou...

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Autores principales: Stickel, Felix, Datz, Christian, Hampe, Jochen, Bataller, Ramon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial Office of Gut and Liver 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5347641/
https://www.ncbi.nlm.nih.gov/pubmed/28274107
http://dx.doi.org/10.5009/gnl16477
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author Stickel, Felix
Datz, Christian
Hampe, Jochen
Bataller, Ramon
author_facet Stickel, Felix
Datz, Christian
Hampe, Jochen
Bataller, Ramon
author_sort Stickel, Felix
collection PubMed
description Alcoholic liver disease (ALD) is a leading cause of cirrhosis, liver cancer, and acute and chronic liver failure and as such causes significant morbidity and mortality. While alcohol consumption is slightly decreasing in several European countries, it is rising in others and remains high in many countries around the world. The pathophysiology of ALD is still incompletely understood but relates largely to the direct toxic effects of alcohol and its main intermediate, acetaldehyde. Recently, novel putative mechanisms have been identified in systematic scans covering the entire human genome and raise new hypotheses on previously unknown pathways. The latter also identify host genetic risk factors for significant liver injury, which may help design prognostic risk scores. The diagnosis of ALD is relatively easy with a panel of well-evaluated tests and only rarely requires a liver biopsy. Treatment of ALD is difficult and grounded in abstinence as the pivotal therapeutic goal; once cirrhosis is established, treatment largely resembles that of other etiologies of advanced liver damage. Liver transplantation is a sound option for carefully selected patients with cirrhosis and alcoholic hepatitis because relapse rates are low and prognosis is comparable to other etiologies. Still, many countries are restrictive in allocating donor livers for ALD patients. Overall, few therapeutic options exist for severe ALD. However, there is good evidence of benefit for only corticosteroids in severe alcoholic hepatitis, while most other efforts are of limited efficacy. Considering the immense burden of ALD worldwide, efforts of medical professionals and industry partners to develop targeted therapies in ALF has been disappointingly low.
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spelling pubmed-53476412017-04-06 Pathophysiology and Management of Alcoholic Liver Disease: Update 2016 Stickel, Felix Datz, Christian Hampe, Jochen Bataller, Ramon Gut Liver Review Alcoholic liver disease (ALD) is a leading cause of cirrhosis, liver cancer, and acute and chronic liver failure and as such causes significant morbidity and mortality. While alcohol consumption is slightly decreasing in several European countries, it is rising in others and remains high in many countries around the world. The pathophysiology of ALD is still incompletely understood but relates largely to the direct toxic effects of alcohol and its main intermediate, acetaldehyde. Recently, novel putative mechanisms have been identified in systematic scans covering the entire human genome and raise new hypotheses on previously unknown pathways. The latter also identify host genetic risk factors for significant liver injury, which may help design prognostic risk scores. The diagnosis of ALD is relatively easy with a panel of well-evaluated tests and only rarely requires a liver biopsy. Treatment of ALD is difficult and grounded in abstinence as the pivotal therapeutic goal; once cirrhosis is established, treatment largely resembles that of other etiologies of advanced liver damage. Liver transplantation is a sound option for carefully selected patients with cirrhosis and alcoholic hepatitis because relapse rates are low and prognosis is comparable to other etiologies. Still, many countries are restrictive in allocating donor livers for ALD patients. Overall, few therapeutic options exist for severe ALD. However, there is good evidence of benefit for only corticosteroids in severe alcoholic hepatitis, while most other efforts are of limited efficacy. Considering the immense burden of ALD worldwide, efforts of medical professionals and industry partners to develop targeted therapies in ALF has been disappointingly low. Editorial Office of Gut and Liver 2017-03 2017-02-21 /pmc/articles/PMC5347641/ /pubmed/28274107 http://dx.doi.org/10.5009/gnl16477 Text en Copyright © 2017 by The Korean Society of Gastroenterology, the Korean Society of Gastrointestinal Endoscopy, the Korean Society of Neurogastroenterology and Motility, Korean College of Helicobacter and Upper Gastrointestinal Research, Korean Association the Study of Intestinal Diseases, the Korean Association for the Study of the Liver, Korean Pancreatobiliary Association, and Korean Society of Gastrointestinal Cancer. This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Stickel, Felix
Datz, Christian
Hampe, Jochen
Bataller, Ramon
Pathophysiology and Management of Alcoholic Liver Disease: Update 2016
title Pathophysiology and Management of Alcoholic Liver Disease: Update 2016
title_full Pathophysiology and Management of Alcoholic Liver Disease: Update 2016
title_fullStr Pathophysiology and Management of Alcoholic Liver Disease: Update 2016
title_full_unstemmed Pathophysiology and Management of Alcoholic Liver Disease: Update 2016
title_short Pathophysiology and Management of Alcoholic Liver Disease: Update 2016
title_sort pathophysiology and management of alcoholic liver disease: update 2016
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5347641/
https://www.ncbi.nlm.nih.gov/pubmed/28274107
http://dx.doi.org/10.5009/gnl16477
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