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Emerging Therapeutic Targets and Experimental Drugs for the Treatment of NAFLD
The two main subsets of nonalcoholic fatty liver disease (NAFLD) include: (1) nonalcoholic fatty liver (NAFL), the more common and non-progressive subtype; and (2) nonalcoholic steatohepatitis (NASH), the less common subtype, which has the potential to progress to advanced liver damage. Current trea...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6164020/ https://www.ncbi.nlm.nih.gov/pubmed/30235807 http://dx.doi.org/10.3390/diseases6030083 |
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author | Dibba, Pratima Li, Andrew A. Perumpail, Brandon J. John, Nimy Sallam, Sandy Shah, Neha D. Kwong, Waiyee Cholankeril, George Kim, Donghee Ahmed, Aijaz |
author_facet | Dibba, Pratima Li, Andrew A. Perumpail, Brandon J. John, Nimy Sallam, Sandy Shah, Neha D. Kwong, Waiyee Cholankeril, George Kim, Donghee Ahmed, Aijaz |
author_sort | Dibba, Pratima |
collection | PubMed |
description | The two main subsets of nonalcoholic fatty liver disease (NAFLD) include: (1) nonalcoholic fatty liver (NAFL), the more common and non-progressive subtype; and (2) nonalcoholic steatohepatitis (NASH), the less common subtype, which has the potential to progress to advanced liver damage. Current treatment strategies have focused on lifestyle management of modifiable risk factors, namely weight, and on the optimization of the management of individual components of metabolic syndrome. Various hypothetical pathogenic mechanisms have been proposed, leading to the development of novel drugs with the potential to effectively treat patients with NASH. Numerous clinical trials are ongoing, utilizing these experimental drugs and molecules targeting specific mechanistic pathway(s) to effectively treat NASH. Some of these mechanistic pathways targeted by experimental pharmacologic agents include chemokine receptor 2 and 5 antagonism, inhibition of galectin-3 protein, antagonism of toll-like receptor 4, variation of fibroblast growth factor 19, agonism of selective thyroid hormone receptor-beta, inhibition of apoptosis signal-regulating kinase 1, inhibition of acetyl-coenzyme A carboxylase, agonism of farnesoid X receptor, antibodies against lysl oxidase-like-2, and inhibition of inflammasomes. Emerging data are promising and further updates from ongoing clinical trials are eagerly awaited. |
format | Online Article Text |
id | pubmed-6164020 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-61640202018-10-11 Emerging Therapeutic Targets and Experimental Drugs for the Treatment of NAFLD Dibba, Pratima Li, Andrew A. Perumpail, Brandon J. John, Nimy Sallam, Sandy Shah, Neha D. Kwong, Waiyee Cholankeril, George Kim, Donghee Ahmed, Aijaz Diseases Review The two main subsets of nonalcoholic fatty liver disease (NAFLD) include: (1) nonalcoholic fatty liver (NAFL), the more common and non-progressive subtype; and (2) nonalcoholic steatohepatitis (NASH), the less common subtype, which has the potential to progress to advanced liver damage. Current treatment strategies have focused on lifestyle management of modifiable risk factors, namely weight, and on the optimization of the management of individual components of metabolic syndrome. Various hypothetical pathogenic mechanisms have been proposed, leading to the development of novel drugs with the potential to effectively treat patients with NASH. Numerous clinical trials are ongoing, utilizing these experimental drugs and molecules targeting specific mechanistic pathway(s) to effectively treat NASH. Some of these mechanistic pathways targeted by experimental pharmacologic agents include chemokine receptor 2 and 5 antagonism, inhibition of galectin-3 protein, antagonism of toll-like receptor 4, variation of fibroblast growth factor 19, agonism of selective thyroid hormone receptor-beta, inhibition of apoptosis signal-regulating kinase 1, inhibition of acetyl-coenzyme A carboxylase, agonism of farnesoid X receptor, antibodies against lysl oxidase-like-2, and inhibition of inflammasomes. Emerging data are promising and further updates from ongoing clinical trials are eagerly awaited. MDPI 2018-09-19 /pmc/articles/PMC6164020/ /pubmed/30235807 http://dx.doi.org/10.3390/diseases6030083 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Dibba, Pratima Li, Andrew A. Perumpail, Brandon J. John, Nimy Sallam, Sandy Shah, Neha D. Kwong, Waiyee Cholankeril, George Kim, Donghee Ahmed, Aijaz Emerging Therapeutic Targets and Experimental Drugs for the Treatment of NAFLD |
title | Emerging Therapeutic Targets and Experimental Drugs for the Treatment of NAFLD |
title_full | Emerging Therapeutic Targets and Experimental Drugs for the Treatment of NAFLD |
title_fullStr | Emerging Therapeutic Targets and Experimental Drugs for the Treatment of NAFLD |
title_full_unstemmed | Emerging Therapeutic Targets and Experimental Drugs for the Treatment of NAFLD |
title_short | Emerging Therapeutic Targets and Experimental Drugs for the Treatment of NAFLD |
title_sort | emerging therapeutic targets and experimental drugs for the treatment of nafld |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6164020/ https://www.ncbi.nlm.nih.gov/pubmed/30235807 http://dx.doi.org/10.3390/diseases6030083 |
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