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Recent advances in understanding/management of non-alcoholic steatohepatitis

Non-alcoholic steatohepatitis (NASH) can lead to advanced fibrosis, hepatocellular carcinoma, and end-stage liver disease requiring liver transplantation. A myriad of pathways and genetic influence contribute to NASH pathogenesis and liver disease progression. Diagnosing patients with NASH and advan...

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Detalles Bibliográficos
Autores principales: Pacana, Tommy, Sanyal, Arun J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Faculty of 1000 Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4371374/
https://www.ncbi.nlm.nih.gov/pubmed/25926979
http://dx.doi.org/10.12703/P7-28
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author Pacana, Tommy
Sanyal, Arun J.
author_facet Pacana, Tommy
Sanyal, Arun J.
author_sort Pacana, Tommy
collection PubMed
description Non-alcoholic steatohepatitis (NASH) can lead to advanced fibrosis, hepatocellular carcinoma, and end-stage liver disease requiring liver transplantation. A myriad of pathways and genetic influence contribute to NASH pathogenesis and liver disease progression. Diagnosing patients with NASH and advanced fibrosis is critical prior to treatment and prognostication. There has been ongoing interest in developing non-invasive biomarkers and tools for identifying NASH and advanced fibrosis. To date, there has been no approved therapy for NASH. Recently, the FLINT (Farnesoid X Receptor [FXR] Ligand Obeticholic Acid in NASH Treatment) trial provided promising results of the efficacy of obeticholic acid, a farnesoid X receptor agonist, in improving histological features of NASH and fibrosis. Long-term studies are needed to assess the safety of obeticholic acid and its effects on liver- and cardiovascular-related outcomes.
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spelling pubmed-43713742015-04-29 Recent advances in understanding/management of non-alcoholic steatohepatitis Pacana, Tommy Sanyal, Arun J. F1000Prime Rep Review Article Non-alcoholic steatohepatitis (NASH) can lead to advanced fibrosis, hepatocellular carcinoma, and end-stage liver disease requiring liver transplantation. A myriad of pathways and genetic influence contribute to NASH pathogenesis and liver disease progression. Diagnosing patients with NASH and advanced fibrosis is critical prior to treatment and prognostication. There has been ongoing interest in developing non-invasive biomarkers and tools for identifying NASH and advanced fibrosis. To date, there has been no approved therapy for NASH. Recently, the FLINT (Farnesoid X Receptor [FXR] Ligand Obeticholic Acid in NASH Treatment) trial provided promising results of the efficacy of obeticholic acid, a farnesoid X receptor agonist, in improving histological features of NASH and fibrosis. Long-term studies are needed to assess the safety of obeticholic acid and its effects on liver- and cardiovascular-related outcomes. Faculty of 1000 Ltd 2015-03-03 /pmc/articles/PMC4371374/ /pubmed/25926979 http://dx.doi.org/10.12703/P7-28 Text en © 2015 Faculty of 1000 Ltd http://creativecommons.org/licenses/by-nc/3.0/legalcode All F1000Prime Reports articles are distributed under the terms of the Creative Commons Attribution-Non Commercial License, which permits non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Pacana, Tommy
Sanyal, Arun J.
Recent advances in understanding/management of non-alcoholic steatohepatitis
title Recent advances in understanding/management of non-alcoholic steatohepatitis
title_full Recent advances in understanding/management of non-alcoholic steatohepatitis
title_fullStr Recent advances in understanding/management of non-alcoholic steatohepatitis
title_full_unstemmed Recent advances in understanding/management of non-alcoholic steatohepatitis
title_short Recent advances in understanding/management of non-alcoholic steatohepatitis
title_sort recent advances in understanding/management of non-alcoholic steatohepatitis
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4371374/
https://www.ncbi.nlm.nih.gov/pubmed/25926979
http://dx.doi.org/10.12703/P7-28
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