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An investigation of thiol/disulfide homeostasis in patients with Behçet’s disease
INTRODUCTION: Behçet’s disease (BD) is a relapsing systemic inflammatory disorder. The diagnosis of BD is primarily based on clinical findings. Current biomarkers are not yet sufficient to diagnose and cannot anticipate the course of the disease and response to treatment. The aim of this study was t...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Termedia Publishing House
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7667443/ https://www.ncbi.nlm.nih.gov/pubmed/33224334 http://dx.doi.org/10.5114/aoms.2019.86703 |
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author | Sandikci, Sevinc Can Colak, Seda Omma, Ahmet Enecik, Mehmet E. Ozbalkan, Zeynep Neselioglu, Salim Erel, Ozcan |
author_facet | Sandikci, Sevinc Can Colak, Seda Omma, Ahmet Enecik, Mehmet E. Ozbalkan, Zeynep Neselioglu, Salim Erel, Ozcan |
author_sort | Sandikci, Sevinc Can |
collection | PubMed |
description | INTRODUCTION: Behçet’s disease (BD) is a relapsing systemic inflammatory disorder. The diagnosis of BD is primarily based on clinical findings. Current biomarkers are not yet sufficient to diagnose and cannot anticipate the course of the disease and response to treatment. The aim of this study was to evaluate the relationship between the thiol-disulfide balance and disease activity and organ involvement in BD. MATERIAL AND METHODS: A hundred fifty patients with BD and 100 age- and gender-matched healthy controls were included in the study. Disease activity was assessed with the BD Current Activity form score. Serum levels of native thiol (NT), total thiol (TT), and disulfide were measured and the disulfide/native thiol, disulfide/total thiol and native thiol/total thiol levels were calculated for the patient and control groups. RESULTS: Native thiol, total thiol, native thiol/total thiol values of the BD patients were significantly lower than those of the control group. The disulfide/native thiol, disulfide/total thiol values of BD patients were higher compared to the control group and the disulfide value of the BD group was slightly higher compared to the control group. No correlation was determined between thiol levels and disease activity and organ involvement in BD. CONCLUSIONS: In patients with Behcet’s disease, the thiol-disulfide homeostasis balance shifted towards disulfide formation due to thiol oxidation. It may be used as a novel marker in BD because it is easy, practical, fully automated and relatively inexpensive. |
format | Online Article Text |
id | pubmed-7667443 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Termedia Publishing House |
record_format | MEDLINE/PubMed |
spelling | pubmed-76674432020-11-20 An investigation of thiol/disulfide homeostasis in patients with Behçet’s disease Sandikci, Sevinc Can Colak, Seda Omma, Ahmet Enecik, Mehmet E. Ozbalkan, Zeynep Neselioglu, Salim Erel, Ozcan Arch Med Sci Clinical Research INTRODUCTION: Behçet’s disease (BD) is a relapsing systemic inflammatory disorder. The diagnosis of BD is primarily based on clinical findings. Current biomarkers are not yet sufficient to diagnose and cannot anticipate the course of the disease and response to treatment. The aim of this study was to evaluate the relationship between the thiol-disulfide balance and disease activity and organ involvement in BD. MATERIAL AND METHODS: A hundred fifty patients with BD and 100 age- and gender-matched healthy controls were included in the study. Disease activity was assessed with the BD Current Activity form score. Serum levels of native thiol (NT), total thiol (TT), and disulfide were measured and the disulfide/native thiol, disulfide/total thiol and native thiol/total thiol levels were calculated for the patient and control groups. RESULTS: Native thiol, total thiol, native thiol/total thiol values of the BD patients were significantly lower than those of the control group. The disulfide/native thiol, disulfide/total thiol values of BD patients were higher compared to the control group and the disulfide value of the BD group was slightly higher compared to the control group. No correlation was determined between thiol levels and disease activity and organ involvement in BD. CONCLUSIONS: In patients with Behcet’s disease, the thiol-disulfide homeostasis balance shifted towards disulfide formation due to thiol oxidation. It may be used as a novel marker in BD because it is easy, practical, fully automated and relatively inexpensive. Termedia Publishing House 2019-07-18 /pmc/articles/PMC7667443/ /pubmed/33224334 http://dx.doi.org/10.5114/aoms.2019.86703 Text en Copyright: © 2019 Termedia & Banach 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 | Clinical Research Sandikci, Sevinc Can Colak, Seda Omma, Ahmet Enecik, Mehmet E. Ozbalkan, Zeynep Neselioglu, Salim Erel, Ozcan An investigation of thiol/disulfide homeostasis in patients with Behçet’s disease |
title | An investigation of thiol/disulfide homeostasis in patients with Behçet’s disease |
title_full | An investigation of thiol/disulfide homeostasis in patients with Behçet’s disease |
title_fullStr | An investigation of thiol/disulfide homeostasis in patients with Behçet’s disease |
title_full_unstemmed | An investigation of thiol/disulfide homeostasis in patients with Behçet’s disease |
title_short | An investigation of thiol/disulfide homeostasis in patients with Behçet’s disease |
title_sort | investigation of thiol/disulfide homeostasis in patients with behçet’s disease |
topic | Clinical Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7667443/ https://www.ncbi.nlm.nih.gov/pubmed/33224334 http://dx.doi.org/10.5114/aoms.2019.86703 |
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