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Glutathione peroxidase and malondialdehyde in children with chronic hepatitis C

AIM OF THE STUDY: We aimed to assess oxidative stress factors, glutathione peroxidase (GPX) and malondialdehyde (MDA) in children with chronic hepatitis C (CHC) and their relation to treatment response. MATERIAL AND METHODS: The study included 50 children with chronic hepatitis C virus (HCV) before...

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Autores principales: Khedr, Mohammed Ahmed, El-Araby, Hanaa Ahmed, Konsowa, Hatem Abdel-Sattar, Sokar, Samia Salem, Mahmoud, Mohammed Fathy, Adawy, Nermin Mohammed, Zakaria, Haidy Mohammed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6431086/
https://www.ncbi.nlm.nih.gov/pubmed/30915411
http://dx.doi.org/10.5114/ceh.2019.83161
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author Khedr, Mohammed Ahmed
El-Araby, Hanaa Ahmed
Konsowa, Hatem Abdel-Sattar
Sokar, Samia Salem
Mahmoud, Mohammed Fathy
Adawy, Nermin Mohammed
Zakaria, Haidy Mohammed
author_facet Khedr, Mohammed Ahmed
El-Araby, Hanaa Ahmed
Konsowa, Hatem Abdel-Sattar
Sokar, Samia Salem
Mahmoud, Mohammed Fathy
Adawy, Nermin Mohammed
Zakaria, Haidy Mohammed
author_sort Khedr, Mohammed Ahmed
collection PubMed
description AIM OF THE STUDY: We aimed to assess oxidative stress factors, glutathione peroxidase (GPX) and malondialdehyde (MDA) in children with chronic hepatitis C (CHC) and their relation to treatment response. MATERIAL AND METHODS: The study included 50 children with chronic hepatitis C virus (HCV) before treatment (naïve HCV), 25 children responders to HCV treatment, 25 children non-responders to HCV treatment and 25 healthy controls. All patients and controls were subjected to GPX and MDA measurement by enzyme-linked immunosorbent assay. RESULTS: The average GPX activity in erythrocytes of naïve CHC patients was 29.2 ±10.3 mU/ml. It was statistically significantly lower than the average activity of GPX in erythrocytes of the healthy control group (47.3 ±5.2 mU/ml) (p < 0.05). The average GPX activity in erythrocytes of the responder group was 34.93 ±3.17 mU/ml. It was statistically significantly higher than the average activity of GPX in erythrocytes of the non-responder group (11.7 ±4.2 mU/ml) (p < 0.05). Plasma MDA was significantly higher in naïve CHC patients than in healthy controls (9.7 ±3.7 nmol/ml vs. 3 ±1.1 nmol/ml, p < 0.0001). Furthermore, plasma MDA concentration was significantly decreased in the responder group (5.36 ±0.7 nmol/ml) and elevated in the non-responder group (16.05 ±2.9 nmol/ml). CONCLUSIONS: Lower pretreatment levels of GPX and higher MDA level might be markers of oxidative stress occurring in HCV patients. Reversal of changes of these levels with completion of the treatment may indicate a correlation between oxidative stress and the viral pathogenesis.
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spelling pubmed-64310862019-03-26 Glutathione peroxidase and malondialdehyde in children with chronic hepatitis C Khedr, Mohammed Ahmed El-Araby, Hanaa Ahmed Konsowa, Hatem Abdel-Sattar Sokar, Samia Salem Mahmoud, Mohammed Fathy Adawy, Nermin Mohammed Zakaria, Haidy Mohammed Clin Exp Hepatol Original Paper AIM OF THE STUDY: We aimed to assess oxidative stress factors, glutathione peroxidase (GPX) and malondialdehyde (MDA) in children with chronic hepatitis C (CHC) and their relation to treatment response. MATERIAL AND METHODS: The study included 50 children with chronic hepatitis C virus (HCV) before treatment (naïve HCV), 25 children responders to HCV treatment, 25 children non-responders to HCV treatment and 25 healthy controls. All patients and controls were subjected to GPX and MDA measurement by enzyme-linked immunosorbent assay. RESULTS: The average GPX activity in erythrocytes of naïve CHC patients was 29.2 ±10.3 mU/ml. It was statistically significantly lower than the average activity of GPX in erythrocytes of the healthy control group (47.3 ±5.2 mU/ml) (p < 0.05). The average GPX activity in erythrocytes of the responder group was 34.93 ±3.17 mU/ml. It was statistically significantly higher than the average activity of GPX in erythrocytes of the non-responder group (11.7 ±4.2 mU/ml) (p < 0.05). Plasma MDA was significantly higher in naïve CHC patients than in healthy controls (9.7 ±3.7 nmol/ml vs. 3 ±1.1 nmol/ml, p < 0.0001). Furthermore, plasma MDA concentration was significantly decreased in the responder group (5.36 ±0.7 nmol/ml) and elevated in the non-responder group (16.05 ±2.9 nmol/ml). CONCLUSIONS: Lower pretreatment levels of GPX and higher MDA level might be markers of oxidative stress occurring in HCV patients. Reversal of changes of these levels with completion of the treatment may indicate a correlation between oxidative stress and the viral pathogenesis. Termedia Publishing House 2019-02-20 2019-03 /pmc/articles/PMC6431086/ /pubmed/30915411 http://dx.doi.org/10.5114/ceh.2019.83161 Text en Copyright: © 2019 Clinical and Experimental Hepatology http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle Original Paper
Khedr, Mohammed Ahmed
El-Araby, Hanaa Ahmed
Konsowa, Hatem Abdel-Sattar
Sokar, Samia Salem
Mahmoud, Mohammed Fathy
Adawy, Nermin Mohammed
Zakaria, Haidy Mohammed
Glutathione peroxidase and malondialdehyde in children with chronic hepatitis C
title Glutathione peroxidase and malondialdehyde in children with chronic hepatitis C
title_full Glutathione peroxidase and malondialdehyde in children with chronic hepatitis C
title_fullStr Glutathione peroxidase and malondialdehyde in children with chronic hepatitis C
title_full_unstemmed Glutathione peroxidase and malondialdehyde in children with chronic hepatitis C
title_short Glutathione peroxidase and malondialdehyde in children with chronic hepatitis C
title_sort glutathione peroxidase and malondialdehyde in children with chronic hepatitis c
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6431086/
https://www.ncbi.nlm.nih.gov/pubmed/30915411
http://dx.doi.org/10.5114/ceh.2019.83161
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