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S100A8/A9 as a biomarker for synovial inflammation and joint damage in patients with rheumatoid arthritis
S100A8 and S100A9 are major leukocyte proteins, known as damage-associated molecular patterns, found at high concentrations in the synovial fluid of patients with rheumatoid arthritis (RA). A heterodimeric complex of S100A8/A9 is secreted by activated leukocytes and binds to Toll-like receptor 4, wh...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Association of Internal Medicine
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3932383/ https://www.ncbi.nlm.nih.gov/pubmed/24574827 http://dx.doi.org/10.3904/kjim.2014.29.1.12 |
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author | Kang, Kwi Young Woo, Jung-Won Park, Sung-Hwan |
author_facet | Kang, Kwi Young Woo, Jung-Won Park, Sung-Hwan |
author_sort | Kang, Kwi Young |
collection | PubMed |
description | S100A8 and S100A9 are major leukocyte proteins, known as damage-associated molecular patterns, found at high concentrations in the synovial fluid of patients with rheumatoid arthritis (RA). A heterodimeric complex of S100A8/A9 is secreted by activated leukocytes and binds to Toll-like receptor 4, which mediates downstream signaling and promotes inflammation and autoimmunity. Serum and synovial fluid levels of S100A8/A9 are markedly higher in patients with RA than in patients with osteoarthritis or miscellaneous inflammatory arthritis. Serum levels of S100A8/A9 are significantly correlated with clinical and laboratory markers of inflammation, such as C-reactive protein, erythrocyte sedimentation rate, rheumatoid factor, and the Disease Activity Score for 28 joints. Significant correlations have also been found between S100A8/A9 and radiographic and clinical assessments of joint damage, such as hand radiographs and the Rheumatoid Arthritis Articular Damage score. In addition, among known inflammatory markers, S100A8/A9 has the strongest correlation with total sum scores of ultrasonography assessment. Furthermore, baseline levels of S100A8/A9 are independently associated with progression of joint destruction in longitudinal studies and are responsive to change during conventional and biologic treatments. These findings suggest S100A8/A9 to be a valuable diagnostic and prognostic biomarker for RA. |
format | Online Article Text |
id | pubmed-3932383 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | The Korean Association of Internal Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-39323832014-02-26 S100A8/A9 as a biomarker for synovial inflammation and joint damage in patients with rheumatoid arthritis Kang, Kwi Young Woo, Jung-Won Park, Sung-Hwan Korean J Intern Med Review S100A8 and S100A9 are major leukocyte proteins, known as damage-associated molecular patterns, found at high concentrations in the synovial fluid of patients with rheumatoid arthritis (RA). A heterodimeric complex of S100A8/A9 is secreted by activated leukocytes and binds to Toll-like receptor 4, which mediates downstream signaling and promotes inflammation and autoimmunity. Serum and synovial fluid levels of S100A8/A9 are markedly higher in patients with RA than in patients with osteoarthritis or miscellaneous inflammatory arthritis. Serum levels of S100A8/A9 are significantly correlated with clinical and laboratory markers of inflammation, such as C-reactive protein, erythrocyte sedimentation rate, rheumatoid factor, and the Disease Activity Score for 28 joints. Significant correlations have also been found between S100A8/A9 and radiographic and clinical assessments of joint damage, such as hand radiographs and the Rheumatoid Arthritis Articular Damage score. In addition, among known inflammatory markers, S100A8/A9 has the strongest correlation with total sum scores of ultrasonography assessment. Furthermore, baseline levels of S100A8/A9 are independently associated with progression of joint destruction in longitudinal studies and are responsive to change during conventional and biologic treatments. These findings suggest S100A8/A9 to be a valuable diagnostic and prognostic biomarker for RA. The Korean Association of Internal Medicine 2014-01 2014-01-02 /pmc/articles/PMC3932383/ /pubmed/24574827 http://dx.doi.org/10.3904/kjim.2014.29.1.12 Text en Copyright © 2014 The Korean Association of Internal Medicine http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Kang, Kwi Young Woo, Jung-Won Park, Sung-Hwan S100A8/A9 as a biomarker for synovial inflammation and joint damage in patients with rheumatoid arthritis |
title | S100A8/A9 as a biomarker for synovial inflammation and joint damage in patients with rheumatoid arthritis |
title_full | S100A8/A9 as a biomarker for synovial inflammation and joint damage in patients with rheumatoid arthritis |
title_fullStr | S100A8/A9 as a biomarker for synovial inflammation and joint damage in patients with rheumatoid arthritis |
title_full_unstemmed | S100A8/A9 as a biomarker for synovial inflammation and joint damage in patients with rheumatoid arthritis |
title_short | S100A8/A9 as a biomarker for synovial inflammation and joint damage in patients with rheumatoid arthritis |
title_sort | s100a8/a9 as a biomarker for synovial inflammation and joint damage in patients with rheumatoid arthritis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3932383/ https://www.ncbi.nlm.nih.gov/pubmed/24574827 http://dx.doi.org/10.3904/kjim.2014.29.1.12 |
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