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Serum Oxidative Stress Markers and Lipidomic Profile to Detect NASH Patients Responsive to an Antioxidant Treatment: A Pilot Study

Liver steatosis can evolve to steatohepatitis (NASH) through a series of biochemical steps related to oxidative stress in hepatocytes. Antioxidants, such as silybin, have been proposed as a treatment of patients with nonalcoholic fatty liver disease (NAFLD) and NASH. In this study, we evaluated, in...

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Autores principales: Stiuso, Paola, Scognamiglio, Ilaria, Murolo, Marianna, Ferranti, Pasquale, De Simone, Carmela, Rizzo, Maria Rosaria, Tuccillo, Concetta, Caraglia, Michele, Loguercio, Carmelina, Federico, Alessandro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4060161/
https://www.ncbi.nlm.nih.gov/pubmed/24987492
http://dx.doi.org/10.1155/2014/169216
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author Stiuso, Paola
Scognamiglio, Ilaria
Murolo, Marianna
Ferranti, Pasquale
De Simone, Carmela
Rizzo, Maria Rosaria
Tuccillo, Concetta
Caraglia, Michele
Loguercio, Carmelina
Federico, Alessandro
author_facet Stiuso, Paola
Scognamiglio, Ilaria
Murolo, Marianna
Ferranti, Pasquale
De Simone, Carmela
Rizzo, Maria Rosaria
Tuccillo, Concetta
Caraglia, Michele
Loguercio, Carmelina
Federico, Alessandro
author_sort Stiuso, Paola
collection PubMed
description Liver steatosis can evolve to steatohepatitis (NASH) through a series of biochemical steps related to oxidative stress in hepatocytes. Antioxidants, such as silybin, have been proposed as a treatment of patients with nonalcoholic fatty liver disease (NAFLD) and NASH. In this study, we evaluated, in patients with histologically documented NASH, the oxidant/antioxidant status and lipid “fingerprint” in the serum of NASH patients, both in basal conditions and after 12 months of treatment with silybin-based food integrator Realsil (RA). The oxidant/antioxidant status analysis showed the presence of a group of patients with higher basal severity of disease (NAS scores 4.67 ± 2.5) and a second group corresponding to borderline NASH (NAS scores = 3.8 ± 1.5). The chronic treatment with RA changed the NAS score in both groups that reached the statistical significance only in group 2, in which there was also a significant decrease of serum lipid peroxidation. The lipidomic profile showed a lipid composition similar to that of healthy subjects with a restoration of the values of free cholesterol, lysoPC, SM, and PC only in group 2 of patients after treatment with RA. Conclusion. These data suggest that lipidomic and/or oxidative status of serum from patients with NASH could be useful as prognostic markers of response to an antioxidant treatment.
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spelling pubmed-40601612014-07-01 Serum Oxidative Stress Markers and Lipidomic Profile to Detect NASH Patients Responsive to an Antioxidant Treatment: A Pilot Study Stiuso, Paola Scognamiglio, Ilaria Murolo, Marianna Ferranti, Pasquale De Simone, Carmela Rizzo, Maria Rosaria Tuccillo, Concetta Caraglia, Michele Loguercio, Carmelina Federico, Alessandro Oxid Med Cell Longev Research Article Liver steatosis can evolve to steatohepatitis (NASH) through a series of biochemical steps related to oxidative stress in hepatocytes. Antioxidants, such as silybin, have been proposed as a treatment of patients with nonalcoholic fatty liver disease (NAFLD) and NASH. In this study, we evaluated, in patients with histologically documented NASH, the oxidant/antioxidant status and lipid “fingerprint” in the serum of NASH patients, both in basal conditions and after 12 months of treatment with silybin-based food integrator Realsil (RA). The oxidant/antioxidant status analysis showed the presence of a group of patients with higher basal severity of disease (NAS scores 4.67 ± 2.5) and a second group corresponding to borderline NASH (NAS scores = 3.8 ± 1.5). The chronic treatment with RA changed the NAS score in both groups that reached the statistical significance only in group 2, in which there was also a significant decrease of serum lipid peroxidation. The lipidomic profile showed a lipid composition similar to that of healthy subjects with a restoration of the values of free cholesterol, lysoPC, SM, and PC only in group 2 of patients after treatment with RA. Conclusion. These data suggest that lipidomic and/or oxidative status of serum from patients with NASH could be useful as prognostic markers of response to an antioxidant treatment. Hindawi Publishing Corporation 2014 2014-06-02 /pmc/articles/PMC4060161/ /pubmed/24987492 http://dx.doi.org/10.1155/2014/169216 Text en Copyright © 2014 Paola Stiuso et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Stiuso, Paola
Scognamiglio, Ilaria
Murolo, Marianna
Ferranti, Pasquale
De Simone, Carmela
Rizzo, Maria Rosaria
Tuccillo, Concetta
Caraglia, Michele
Loguercio, Carmelina
Federico, Alessandro
Serum Oxidative Stress Markers and Lipidomic Profile to Detect NASH Patients Responsive to an Antioxidant Treatment: A Pilot Study
title Serum Oxidative Stress Markers and Lipidomic Profile to Detect NASH Patients Responsive to an Antioxidant Treatment: A Pilot Study
title_full Serum Oxidative Stress Markers and Lipidomic Profile to Detect NASH Patients Responsive to an Antioxidant Treatment: A Pilot Study
title_fullStr Serum Oxidative Stress Markers and Lipidomic Profile to Detect NASH Patients Responsive to an Antioxidant Treatment: A Pilot Study
title_full_unstemmed Serum Oxidative Stress Markers and Lipidomic Profile to Detect NASH Patients Responsive to an Antioxidant Treatment: A Pilot Study
title_short Serum Oxidative Stress Markers and Lipidomic Profile to Detect NASH Patients Responsive to an Antioxidant Treatment: A Pilot Study
title_sort serum oxidative stress markers and lipidomic profile to detect nash patients responsive to an antioxidant treatment: a pilot study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4060161/
https://www.ncbi.nlm.nih.gov/pubmed/24987492
http://dx.doi.org/10.1155/2014/169216
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