Cargando…

Nonalcoholic fatty liver disease: new treatments

PURPOSE OF REVIEW: Nonalcoholic fatty liver disease is the most common cause of liver dysfunction in the western world because of its close association with obesity, insulin resistance and dyslipidaemia. Nonalcoholic steatohepatitis (NASH) is a particular health concern due to the increased morbidit...

Descripción completa

Detalles Bibliográficos
Autores principales: Hardy, Timothy, Anstee, Quentin M., Day, Christopher P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4482455/
https://www.ncbi.nlm.nih.gov/pubmed/25774446
http://dx.doi.org/10.1097/MOG.0000000000000175
_version_ 1782378445761675264
author Hardy, Timothy
Anstee, Quentin M.
Day, Christopher P.
author_facet Hardy, Timothy
Anstee, Quentin M.
Day, Christopher P.
author_sort Hardy, Timothy
collection PubMed
description PURPOSE OF REVIEW: Nonalcoholic fatty liver disease is the most common cause of liver dysfunction in the western world because of its close association with obesity, insulin resistance and dyslipidaemia. Nonalcoholic steatohepatitis (NASH) is a particular health concern due to the increased morbidity and mortality associated with progressive disease. At present, without specific targeted pharmacological therapies, the mainstay of therapy remains weight loss through dietary modification and lifestyle change; thus, the purpose of this review is to summarize the recent evidence for current and emerging therapies in NASH. RECENT FINDINGS: Some existing medications, including pioglitazones and angiotensin receptor antagonists, may be repurposed to help treat this condition. Vitamin E may improve histology in NASH, but safety issues limit its use. Recently, a number of novel agents specifically targeting nonalcoholic fatty liver disease pathogenesis have entered clinical trials, including the farnesoid X receptor agonist obeticholic acid, which has shown significant histological improvements in steatohepatitis and fibrosis. SUMMARY: Diet/lifestyle modification remains the mainstay of treatment. For patients with NASH and advanced fibrosis, current liver-directed pharmacotherapy with vitamin E and pioglitazone offer some benefits; obeticholic acid appears promising and is currently being tested. Comorbidities must be diagnosed and treated; cardiovascular disease remains a primary cause of death in these patients.
format Online
Article
Text
id pubmed-4482455
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Lippincott Williams & Wilkins
record_format MEDLINE/PubMed
spelling pubmed-44824552015-07-07 Nonalcoholic fatty liver disease: new treatments Hardy, Timothy Anstee, Quentin M. Day, Christopher P. Curr Opin Gastroenterol LIVER: Edited by Don C. Rockey PURPOSE OF REVIEW: Nonalcoholic fatty liver disease is the most common cause of liver dysfunction in the western world because of its close association with obesity, insulin resistance and dyslipidaemia. Nonalcoholic steatohepatitis (NASH) is a particular health concern due to the increased morbidity and mortality associated with progressive disease. At present, without specific targeted pharmacological therapies, the mainstay of therapy remains weight loss through dietary modification and lifestyle change; thus, the purpose of this review is to summarize the recent evidence for current and emerging therapies in NASH. RECENT FINDINGS: Some existing medications, including pioglitazones and angiotensin receptor antagonists, may be repurposed to help treat this condition. Vitamin E may improve histology in NASH, but safety issues limit its use. Recently, a number of novel agents specifically targeting nonalcoholic fatty liver disease pathogenesis have entered clinical trials, including the farnesoid X receptor agonist obeticholic acid, which has shown significant histological improvements in steatohepatitis and fibrosis. SUMMARY: Diet/lifestyle modification remains the mainstay of treatment. For patients with NASH and advanced fibrosis, current liver-directed pharmacotherapy with vitamin E and pioglitazone offer some benefits; obeticholic acid appears promising and is currently being tested. Comorbidities must be diagnosed and treated; cardiovascular disease remains a primary cause of death in these patients. Lippincott Williams & Wilkins 2015-05 2015-04-15 /pmc/articles/PMC4482455/ /pubmed/25774446 http://dx.doi.org/10.1097/MOG.0000000000000175 Text en Copyright © 2015 Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License, where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially. http://creativecommons.org/licenses/by-nc-nd/4.0
spellingShingle LIVER: Edited by Don C. Rockey
Hardy, Timothy
Anstee, Quentin M.
Day, Christopher P.
Nonalcoholic fatty liver disease: new treatments
title Nonalcoholic fatty liver disease: new treatments
title_full Nonalcoholic fatty liver disease: new treatments
title_fullStr Nonalcoholic fatty liver disease: new treatments
title_full_unstemmed Nonalcoholic fatty liver disease: new treatments
title_short Nonalcoholic fatty liver disease: new treatments
title_sort nonalcoholic fatty liver disease: new treatments
topic LIVER: Edited by Don C. Rockey
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4482455/
https://www.ncbi.nlm.nih.gov/pubmed/25774446
http://dx.doi.org/10.1097/MOG.0000000000000175
work_keys_str_mv AT hardytimothy nonalcoholicfattyliverdiseasenewtreatments
AT ansteequentinm nonalcoholicfattyliverdiseasenewtreatments
AT daychristopherp nonalcoholicfattyliverdiseasenewtreatments