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Inositol and Non-Alcoholic Fatty Liver Disease: A Systematic Review on Deficiencies and Supplementation
Liver lipid accumulation is a hallmark of non-alcoholic fatty liver disease (NAFLD), broadly associated with insulin resistance. Inositols (INS) are ubiquitous polyols implied in many physiological functions. They are produced endogenously, are present in many foods and in dietary supplements. Alter...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7694137/ https://www.ncbi.nlm.nih.gov/pubmed/33153126 http://dx.doi.org/10.3390/nu12113379 |
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author | Pani, Arianna Giossi, Riccardo Menichelli, Danilo Fittipaldo, Veronica Andrea Agnelli, Francesca Inglese, Elvira Romandini, Alessandra Roncato, Rossana Pintaudi, Basilio Del Sole, Francesco Scaglione, Francesco |
author_facet | Pani, Arianna Giossi, Riccardo Menichelli, Danilo Fittipaldo, Veronica Andrea Agnelli, Francesca Inglese, Elvira Romandini, Alessandra Roncato, Rossana Pintaudi, Basilio Del Sole, Francesco Scaglione, Francesco |
author_sort | Pani, Arianna |
collection | PubMed |
description | Liver lipid accumulation is a hallmark of non-alcoholic fatty liver disease (NAFLD), broadly associated with insulin resistance. Inositols (INS) are ubiquitous polyols implied in many physiological functions. They are produced endogenously, are present in many foods and in dietary supplements. Alterations in INS metabolism seems to play a role in diseases involving insulin resistance such as diabetes and polycystic ovary syndrome. Given its role in other metabolic syndromes, the hypothesis of an INS role as a supplement in NAFLD is intriguing. We performed a systematic review of the literature to find preclinical and clinical evidence of INS supplementation efficacy in NAFLD patients. We retrieved 10 studies on animal models assessing Myoinosiol or Pinitol deficiency or supplementation and one human randomized controlled trial (RCT). Overall, INS deficiency was associated with increased fatty liver in animals. Conversely, INS supplementation in animal models of fatty liver reduced hepatic triglycerides and cholesterol accumulation and maintained a normal ultrastructural liver histopathology. In the one included RCT, Pinitol supplementation obtained similar results. Pinitol significantly reduced liver fat, post-prandial triglycerides, AST levels, lipid peroxidation increasing glutathione peroxidase activity. These results, despite being limited, indicate the need for further evaluation of INS in NAFLD in larger clinical trials. |
format | Online Article Text |
id | pubmed-7694137 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-76941372020-11-28 Inositol and Non-Alcoholic Fatty Liver Disease: A Systematic Review on Deficiencies and Supplementation Pani, Arianna Giossi, Riccardo Menichelli, Danilo Fittipaldo, Veronica Andrea Agnelli, Francesca Inglese, Elvira Romandini, Alessandra Roncato, Rossana Pintaudi, Basilio Del Sole, Francesco Scaglione, Francesco Nutrients Review Liver lipid accumulation is a hallmark of non-alcoholic fatty liver disease (NAFLD), broadly associated with insulin resistance. Inositols (INS) are ubiquitous polyols implied in many physiological functions. They are produced endogenously, are present in many foods and in dietary supplements. Alterations in INS metabolism seems to play a role in diseases involving insulin resistance such as diabetes and polycystic ovary syndrome. Given its role in other metabolic syndromes, the hypothesis of an INS role as a supplement in NAFLD is intriguing. We performed a systematic review of the literature to find preclinical and clinical evidence of INS supplementation efficacy in NAFLD patients. We retrieved 10 studies on animal models assessing Myoinosiol or Pinitol deficiency or supplementation and one human randomized controlled trial (RCT). Overall, INS deficiency was associated with increased fatty liver in animals. Conversely, INS supplementation in animal models of fatty liver reduced hepatic triglycerides and cholesterol accumulation and maintained a normal ultrastructural liver histopathology. In the one included RCT, Pinitol supplementation obtained similar results. Pinitol significantly reduced liver fat, post-prandial triglycerides, AST levels, lipid peroxidation increasing glutathione peroxidase activity. These results, despite being limited, indicate the need for further evaluation of INS in NAFLD in larger clinical trials. MDPI 2020-11-03 /pmc/articles/PMC7694137/ /pubmed/33153126 http://dx.doi.org/10.3390/nu12113379 Text en © 2020 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 Pani, Arianna Giossi, Riccardo Menichelli, Danilo Fittipaldo, Veronica Andrea Agnelli, Francesca Inglese, Elvira Romandini, Alessandra Roncato, Rossana Pintaudi, Basilio Del Sole, Francesco Scaglione, Francesco Inositol and Non-Alcoholic Fatty Liver Disease: A Systematic Review on Deficiencies and Supplementation |
title | Inositol and Non-Alcoholic Fatty Liver Disease: A Systematic Review on Deficiencies and Supplementation |
title_full | Inositol and Non-Alcoholic Fatty Liver Disease: A Systematic Review on Deficiencies and Supplementation |
title_fullStr | Inositol and Non-Alcoholic Fatty Liver Disease: A Systematic Review on Deficiencies and Supplementation |
title_full_unstemmed | Inositol and Non-Alcoholic Fatty Liver Disease: A Systematic Review on Deficiencies and Supplementation |
title_short | Inositol and Non-Alcoholic Fatty Liver Disease: A Systematic Review on Deficiencies and Supplementation |
title_sort | inositol and non-alcoholic fatty liver disease: a systematic review on deficiencies and supplementation |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7694137/ https://www.ncbi.nlm.nih.gov/pubmed/33153126 http://dx.doi.org/10.3390/nu12113379 |
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