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Recent advances in nonalcoholic fatty liver disease metabolomics

The clinical phenotypes of nonalcoholic fatty liver disease (NAFLD) encompass from simple steatosis to nonalcoholic steatohepatitis (NASH) with varying degrees of fibrosis or cirrhosis. Liver biopsy has been the standard to diagnose NASH. However, there has been strong need for precise and accurate...

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Autor principal: Kim, Hwi Young
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Association for the Study of the Liver 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8524071/
https://www.ncbi.nlm.nih.gov/pubmed/34098712
http://dx.doi.org/10.3350/cmh.2021.0127
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author Kim, Hwi Young
author_facet Kim, Hwi Young
author_sort Kim, Hwi Young
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description The clinical phenotypes of nonalcoholic fatty liver disease (NAFLD) encompass from simple steatosis to nonalcoholic steatohepatitis (NASH) with varying degrees of fibrosis or cirrhosis. Liver biopsy has been the standard to diagnose NASH. However, there has been strong need for precise and accurate noninvasive tests because of invasiveness and sampling variability of biopsy. Metabolomics has drawn attention as a promising diagnostic methodology in the field of NAFLD, particularly to unravel metabolic alterations which plays relevant roles in the progression of NASH. There have been numerous metabolomics researches to find new biomarker of NASH in the last decade, fueled by the recent advances in the metabolomics methodology. This review briefly covers recent research advances on the lipidomics, amino acids and bile acid metabolomics regarding continuing attempts to discover relevant biomarkers for NASH.
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spelling pubmed-85240712021-10-29 Recent advances in nonalcoholic fatty liver disease metabolomics Kim, Hwi Young Clin Mol Hepatol Review The clinical phenotypes of nonalcoholic fatty liver disease (NAFLD) encompass from simple steatosis to nonalcoholic steatohepatitis (NASH) with varying degrees of fibrosis or cirrhosis. Liver biopsy has been the standard to diagnose NASH. However, there has been strong need for precise and accurate noninvasive tests because of invasiveness and sampling variability of biopsy. Metabolomics has drawn attention as a promising diagnostic methodology in the field of NAFLD, particularly to unravel metabolic alterations which plays relevant roles in the progression of NASH. There have been numerous metabolomics researches to find new biomarker of NASH in the last decade, fueled by the recent advances in the metabolomics methodology. This review briefly covers recent research advances on the lipidomics, amino acids and bile acid metabolomics regarding continuing attempts to discover relevant biomarkers for NASH. The Korean Association for the Study of the Liver 2021-10 2021-06-08 /pmc/articles/PMC8524071/ /pubmed/34098712 http://dx.doi.org/10.3350/cmh.2021.0127 Text en Copyright © 2021 by The Korean Association for the Study of the Liver https://creativecommons.org/licenses/by-nc/3.0/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/ (https://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
Kim, Hwi Young
Recent advances in nonalcoholic fatty liver disease metabolomics
title Recent advances in nonalcoholic fatty liver disease metabolomics
title_full Recent advances in nonalcoholic fatty liver disease metabolomics
title_fullStr Recent advances in nonalcoholic fatty liver disease metabolomics
title_full_unstemmed Recent advances in nonalcoholic fatty liver disease metabolomics
title_short Recent advances in nonalcoholic fatty liver disease metabolomics
title_sort recent advances in nonalcoholic fatty liver disease metabolomics
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8524071/
https://www.ncbi.nlm.nih.gov/pubmed/34098712
http://dx.doi.org/10.3350/cmh.2021.0127
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