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Increased Reactive Oxygen Species Formation and Oxidative Stress in Rheumatoid Arthritis
BACKGROUND: Rheumatoid arthritis (RA) is an autoimmune inflammatory disorder. Highly reactive oxygen free radicals are believed to be involved in the pathogenesis of the disease. In this study, RA patients were sub-grouped depending upon the presence or absence of rheumatoid factor, disease activity...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4820274/ https://www.ncbi.nlm.nih.gov/pubmed/27043143 http://dx.doi.org/10.1371/journal.pone.0152925 |
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author | Mateen, Somaiya Moin, Shagufta Khan, Abdul Qayyum Zafar, Atif Fatima, Naureen |
author_facet | Mateen, Somaiya Moin, Shagufta Khan, Abdul Qayyum Zafar, Atif Fatima, Naureen |
author_sort | Mateen, Somaiya |
collection | PubMed |
description | BACKGROUND: Rheumatoid arthritis (RA) is an autoimmune inflammatory disorder. Highly reactive oxygen free radicals are believed to be involved in the pathogenesis of the disease. In this study, RA patients were sub-grouped depending upon the presence or absence of rheumatoid factor, disease activity score and disease duration. RA Patients (120) and healthy controls (53) were evaluated for the oxidant—antioxidant status by monitoring ROS production, biomarkers of lipid peroxidation, protein oxidation and DNA damage. The level of various enzymatic and non-enzymatic antioxidants was also monitored. Correlation analysis was also performed for analysing the association between ROS and various other parameters. METHODS: Intracellular ROS formation, lipid peroxidation (MDA level), protein oxidation (carbonyl level and thiol level) and DNA damage were detected in the blood of RA patients. Antioxidant status was evaluated by FRAP assay, DPPH reduction assay and enzymatic (SOD, catalase, GST, GR) and non-enzymatic (vitamin C and GSH) antioxidants. RESULTS: RA patients showed a higher ROS production, increased lipid peroxidation, protein oxidation and DNA damage. A significant decline in the ferric reducing ability, DPPH radical quenching ability and the levels of antioxidants has also been observed. Significant correlation has been found between ROS and various other parameters studied. CONCLUSION: RA patients showed a marked increase in ROS formation, lipid peroxidation, protein oxidation, DNA damage and decrease in the activity of antioxidant defence system leading to oxidative stress which may contribute to tissue damage and hence to the chronicity of the disease. |
format | Online Article Text |
id | pubmed-4820274 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-48202742016-04-22 Increased Reactive Oxygen Species Formation and Oxidative Stress in Rheumatoid Arthritis Mateen, Somaiya Moin, Shagufta Khan, Abdul Qayyum Zafar, Atif Fatima, Naureen PLoS One Research Article BACKGROUND: Rheumatoid arthritis (RA) is an autoimmune inflammatory disorder. Highly reactive oxygen free radicals are believed to be involved in the pathogenesis of the disease. In this study, RA patients were sub-grouped depending upon the presence or absence of rheumatoid factor, disease activity score and disease duration. RA Patients (120) and healthy controls (53) were evaluated for the oxidant—antioxidant status by monitoring ROS production, biomarkers of lipid peroxidation, protein oxidation and DNA damage. The level of various enzymatic and non-enzymatic antioxidants was also monitored. Correlation analysis was also performed for analysing the association between ROS and various other parameters. METHODS: Intracellular ROS formation, lipid peroxidation (MDA level), protein oxidation (carbonyl level and thiol level) and DNA damage were detected in the blood of RA patients. Antioxidant status was evaluated by FRAP assay, DPPH reduction assay and enzymatic (SOD, catalase, GST, GR) and non-enzymatic (vitamin C and GSH) antioxidants. RESULTS: RA patients showed a higher ROS production, increased lipid peroxidation, protein oxidation and DNA damage. A significant decline in the ferric reducing ability, DPPH radical quenching ability and the levels of antioxidants has also been observed. Significant correlation has been found between ROS and various other parameters studied. CONCLUSION: RA patients showed a marked increase in ROS formation, lipid peroxidation, protein oxidation, DNA damage and decrease in the activity of antioxidant defence system leading to oxidative stress which may contribute to tissue damage and hence to the chronicity of the disease. Public Library of Science 2016-04-04 /pmc/articles/PMC4820274/ /pubmed/27043143 http://dx.doi.org/10.1371/journal.pone.0152925 Text en © 2016 Mateen et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Mateen, Somaiya Moin, Shagufta Khan, Abdul Qayyum Zafar, Atif Fatima, Naureen Increased Reactive Oxygen Species Formation and Oxidative Stress in Rheumatoid Arthritis |
title | Increased Reactive Oxygen Species Formation and Oxidative Stress in Rheumatoid Arthritis |
title_full | Increased Reactive Oxygen Species Formation and Oxidative Stress in Rheumatoid Arthritis |
title_fullStr | Increased Reactive Oxygen Species Formation and Oxidative Stress in Rheumatoid Arthritis |
title_full_unstemmed | Increased Reactive Oxygen Species Formation and Oxidative Stress in Rheumatoid Arthritis |
title_short | Increased Reactive Oxygen Species Formation and Oxidative Stress in Rheumatoid Arthritis |
title_sort | increased reactive oxygen species formation and oxidative stress in rheumatoid arthritis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4820274/ https://www.ncbi.nlm.nih.gov/pubmed/27043143 http://dx.doi.org/10.1371/journal.pone.0152925 |
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