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Contribution of Metabolomics to the Understanding of NAFLD and NASH Syndromes: A Systematic Review
Several differential panels of metabolites have been associated with the presence of metabolic syndrome and its related conditions, namely non-alcoholic fatty liver disease (NAFLD) and non-alcoholic steatohepatitis (NASH). This study aimed to perform a systematic review to summarize the most recent...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8541039/ https://www.ncbi.nlm.nih.gov/pubmed/34677409 http://dx.doi.org/10.3390/metabo11100694 |
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author | Piras, Cristina Noto, Antonio Ibba, Luciano Deidda, Martino Fanos, Vassilios Muntoni, Sandro Leoni, Vera Piera Atzori, Luigi |
author_facet | Piras, Cristina Noto, Antonio Ibba, Luciano Deidda, Martino Fanos, Vassilios Muntoni, Sandro Leoni, Vera Piera Atzori, Luigi |
author_sort | Piras, Cristina |
collection | PubMed |
description | Several differential panels of metabolites have been associated with the presence of metabolic syndrome and its related conditions, namely non-alcoholic fatty liver disease (NAFLD) and non-alcoholic steatohepatitis (NASH). This study aimed to perform a systematic review to summarize the most recent finding in terms of circulating biomarkers following NAFLD/NASH syndromes. Hence, the research was focused on NAFLD/NASH studies analysed by metabolomics approaches. Following Preferred Reporting Items for Systematic Reviews and Meta-analysis (PRISMA) guidelines, a systematic search was conducted on the PubMed database. The inclusion criteria were (i) publication date between 2010 and 2021, (ii) presence of the combination of terms: metabolomics and NAFLD/NASH, and (iii) published in a scholarly peer-reviewed journal. Studies were excluded from the review if they were (i) single-case studies, (ii) unpublished thesis and dissertation studies, and (iii) not published in a peer-reviewed journal. Following these procedures, 10 eligible studies among 93 were taken into consideration. The metabolisms of amino acids, fatty acid, and vitamins were significantly different in patients affected by NAFLD and NASH compared to healthy controls. These findings suggest that low weight metabolites are an important indicator for NAFLD/NASH syndrome and there is a strong overlap between NAFLD/NASH and the metabolic syndrome. These findings may lead to new perspectives in early diagnosis, identification of novel biomarkers, and providing novel targets for pharmacological interventions. |
format | Online Article Text |
id | pubmed-8541039 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-85410392021-10-24 Contribution of Metabolomics to the Understanding of NAFLD and NASH Syndromes: A Systematic Review Piras, Cristina Noto, Antonio Ibba, Luciano Deidda, Martino Fanos, Vassilios Muntoni, Sandro Leoni, Vera Piera Atzori, Luigi Metabolites Systematic Review Several differential panels of metabolites have been associated with the presence of metabolic syndrome and its related conditions, namely non-alcoholic fatty liver disease (NAFLD) and non-alcoholic steatohepatitis (NASH). This study aimed to perform a systematic review to summarize the most recent finding in terms of circulating biomarkers following NAFLD/NASH syndromes. Hence, the research was focused on NAFLD/NASH studies analysed by metabolomics approaches. Following Preferred Reporting Items for Systematic Reviews and Meta-analysis (PRISMA) guidelines, a systematic search was conducted on the PubMed database. The inclusion criteria were (i) publication date between 2010 and 2021, (ii) presence of the combination of terms: metabolomics and NAFLD/NASH, and (iii) published in a scholarly peer-reviewed journal. Studies were excluded from the review if they were (i) single-case studies, (ii) unpublished thesis and dissertation studies, and (iii) not published in a peer-reviewed journal. Following these procedures, 10 eligible studies among 93 were taken into consideration. The metabolisms of amino acids, fatty acid, and vitamins were significantly different in patients affected by NAFLD and NASH compared to healthy controls. These findings suggest that low weight metabolites are an important indicator for NAFLD/NASH syndrome and there is a strong overlap between NAFLD/NASH and the metabolic syndrome. These findings may lead to new perspectives in early diagnosis, identification of novel biomarkers, and providing novel targets for pharmacological interventions. MDPI 2021-10-11 /pmc/articles/PMC8541039/ /pubmed/34677409 http://dx.doi.org/10.3390/metabo11100694 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Systematic Review Piras, Cristina Noto, Antonio Ibba, Luciano Deidda, Martino Fanos, Vassilios Muntoni, Sandro Leoni, Vera Piera Atzori, Luigi Contribution of Metabolomics to the Understanding of NAFLD and NASH Syndromes: A Systematic Review |
title | Contribution of Metabolomics to the Understanding of NAFLD and NASH Syndromes: A Systematic Review |
title_full | Contribution of Metabolomics to the Understanding of NAFLD and NASH Syndromes: A Systematic Review |
title_fullStr | Contribution of Metabolomics to the Understanding of NAFLD and NASH Syndromes: A Systematic Review |
title_full_unstemmed | Contribution of Metabolomics to the Understanding of NAFLD and NASH Syndromes: A Systematic Review |
title_short | Contribution of Metabolomics to the Understanding of NAFLD and NASH Syndromes: A Systematic Review |
title_sort | contribution of metabolomics to the understanding of nafld and nash syndromes: a systematic review |
topic | Systematic Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8541039/ https://www.ncbi.nlm.nih.gov/pubmed/34677409 http://dx.doi.org/10.3390/metabo11100694 |
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