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The Importance of HLA-B27 in the Evolution of Reactive Arthritis
Reactive arthritis is an inflammatory joint disease which develops after 1-4 weeks following an enteral, genital or ORL infection, with a higher frequency in HLA-B27 positive patients. AIMS: The objective of this paper is to study the importance of HLA-B27 antigen in the development of reactive arth...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medical University Publishing House Craiova
201
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7014986/ https://www.ncbi.nlm.nih.gov/pubmed/32110435 http://dx.doi.org/10.12865/CHSJ.45.04.01 |
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author | BĂNICIOIU-COVEI, S VREJU, AF ROSU, A CIUREA, PL |
author_facet | BĂNICIOIU-COVEI, S VREJU, AF ROSU, A CIUREA, PL |
author_sort | BĂNICIOIU-COVEI, S |
collection | PubMed |
description | Reactive arthritis is an inflammatory joint disease which develops after 1-4 weeks following an enteral, genital or ORL infection, with a higher frequency in HLA-B27 positive patients. AIMS: The objective of this paper is to study the importance of HLA-B27 antigen in the development of reactive arthritis. Patients and methods. The transversal, observational study was conducted in the Rheumatology Clinic of the University of Medicine and Pharmacy of Craiova during the period 2012-2015 and included 112 patients. They were divided into three groups, as follows: group I (52 reactive arthritis cases), group II (30 other spondyloarthritis cases), group III (40 osteoarthritis cases). ELISA and PCR techniques were used to determine the antigen. Results. Those whom had this genetic marker present, the number of enthesitis almost doubled highlighting a possible correlation between the antigen and these imaging changes. We can confirm the same thing for the erosions as well. Unlike enthesitis, erosions occurred also in group III (37.5%), but if we refer to the first two groups, we will observe a significant relationship regarding HLA-B27. More specifically, in HLA-B27 positive patients (68.97%), erosions were found to be twice as numerous than in HLA-B27 negative patients (31.03%). In group I we identified stage 2 sacroiliitis in 68% of HLA-B27 positive patients and 32% in HLA-B27 negative, which shows another link to this antigen with both joint destruction and a possible unfavorable evolution of reactive arthritis. Conclusions. This antigen specific to the seronegative group of spondyloarthritis determines the acceleration of articular destruction, translated by erosion, and the evolution of sacroiliitis to a more advanced stage. |
format | Online Article Text |
id | pubmed-7014986 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 201 |
publisher | Medical University Publishing House Craiova |
record_format | MEDLINE/PubMed |
spelling | pubmed-70149862020-02-27 The Importance of HLA-B27 in the Evolution of Reactive Arthritis BĂNICIOIU-COVEI, S VREJU, AF ROSU, A CIUREA, PL Curr Health Sci J Original Paper Reactive arthritis is an inflammatory joint disease which develops after 1-4 weeks following an enteral, genital or ORL infection, with a higher frequency in HLA-B27 positive patients. AIMS: The objective of this paper is to study the importance of HLA-B27 antigen in the development of reactive arthritis. Patients and methods. The transversal, observational study was conducted in the Rheumatology Clinic of the University of Medicine and Pharmacy of Craiova during the period 2012-2015 and included 112 patients. They were divided into three groups, as follows: group I (52 reactive arthritis cases), group II (30 other spondyloarthritis cases), group III (40 osteoarthritis cases). ELISA and PCR techniques were used to determine the antigen. Results. Those whom had this genetic marker present, the number of enthesitis almost doubled highlighting a possible correlation between the antigen and these imaging changes. We can confirm the same thing for the erosions as well. Unlike enthesitis, erosions occurred also in group III (37.5%), but if we refer to the first two groups, we will observe a significant relationship regarding HLA-B27. More specifically, in HLA-B27 positive patients (68.97%), erosions were found to be twice as numerous than in HLA-B27 negative patients (31.03%). In group I we identified stage 2 sacroiliitis in 68% of HLA-B27 positive patients and 32% in HLA-B27 negative, which shows another link to this antigen with both joint destruction and a possible unfavorable evolution of reactive arthritis. Conclusions. This antigen specific to the seronegative group of spondyloarthritis determines the acceleration of articular destruction, translated by erosion, and the evolution of sacroiliitis to a more advanced stage. Medical University Publishing House Craiova 2019 2019-12-30 /pmc/articles/PMC7014986/ /pubmed/32110435 http://dx.doi.org/10.12865/CHSJ.45.04.01 Text en Copyright © 2019, Medical University Publishing House Craiova http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an open-access article distributed under the terms of a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Public License, which permits unrestricted use, adaptation, distribution and reproduction in any medium, non-commercially, provided the new creations are licensed under identical terms as the original work and the original work is properly cited. |
spellingShingle | Original Paper BĂNICIOIU-COVEI, S VREJU, AF ROSU, A CIUREA, PL The Importance of HLA-B27 in the Evolution of Reactive Arthritis |
title | The Importance of HLA-B27 in the Evolution of Reactive Arthritis |
title_full | The Importance of HLA-B27 in the Evolution of Reactive Arthritis |
title_fullStr | The Importance of HLA-B27 in the Evolution of Reactive Arthritis |
title_full_unstemmed | The Importance of HLA-B27 in the Evolution of Reactive Arthritis |
title_short | The Importance of HLA-B27 in the Evolution of Reactive Arthritis |
title_sort | importance of hla-b27 in the evolution of reactive arthritis |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7014986/ https://www.ncbi.nlm.nih.gov/pubmed/32110435 http://dx.doi.org/10.12865/CHSJ.45.04.01 |
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