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Association of cytokine and matrix metalloproteinase profiles with disease activity and function in ankylosing spondylitis
INTRODUCTION: The pathology of ankylosing spondylitis (AS) suggests that certain cytokines and matrix metalloproteinases (MMPs) might provide useful markers of disease activity. Serum levels of some cytokines and MMPs have been found to be elevated in active disease, but there is a general lack of i...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3446508/ https://www.ncbi.nlm.nih.gov/pubmed/22640827 http://dx.doi.org/10.1186/ar3857 |
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author | Mattey, Derek L Packham, Jonathan C Nixon, Nicola B Coates, Lucy Creamer, Paul Hailwood, Sarah Taylor, Gordon J Bhalla, Ashok K |
author_facet | Mattey, Derek L Packham, Jonathan C Nixon, Nicola B Coates, Lucy Creamer, Paul Hailwood, Sarah Taylor, Gordon J Bhalla, Ashok K |
author_sort | Mattey, Derek L |
collection | PubMed |
description | INTRODUCTION: The pathology of ankylosing spondylitis (AS) suggests that certain cytokines and matrix metalloproteinases (MMPs) might provide useful markers of disease activity. Serum levels of some cytokines and MMPs have been found to be elevated in active disease, but there is a general lack of information about biomarker profiles in AS and how these are related to disease activity and function. The purpose of this study was to investigate whether clinical measures of disease activity and function in AS are associated with particular profiles of circulating cytokines and MMPs. METHODS: Measurement of 30 cytokines, five MMPs and four tissue inhibitors of metalloproteinases was carried out using Luminex(® )technology on a well-characterised population of AS patients (n = 157). The relationship between biomarker levels and measures of disease activity (Bath ankylosing spondylitis disease activity index (BASDAI)), function (Bath ankylosing spondylitis functional index) and global health (Bath ankylosing spondylitis global health) was investigated. Principal component analysis was used to reduce the large number of biomarkers to a smaller set of independent components, which were investigated for their association with clinical measures. Further analyses were carried out using hierarchical clustering, multiple regression or multivariate logistic regression. RESULTS: Principal component analysis identified eight clusters consisting of various combinations of cytokines and MMPs. The strongest association with the BASDAI was found with a component consisting of MMP-8, MMP-9, hepatocyte growth factor and CXCL8, and was independent of C-reactive protein levels. This component was also associated with current smoking. Hierarchical clustering revealed two distinct patient clusters that could be separated on the basis of MMP levels. The high MMP cluster was associated with increased C-reactive protein, the BASDAI and the Bath ankylosing spondylitis functional index. CONCLUSIONS: A profile consisting of high levels of MMP-8, MMP-9, hepatocyte growth factor and CXCL8 is associated with increased disease activity in AS. High MMP levels are also associated with smoking and worse function in AS. |
format | Online Article Text |
id | pubmed-3446508 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-34465082012-09-20 Association of cytokine and matrix metalloproteinase profiles with disease activity and function in ankylosing spondylitis Mattey, Derek L Packham, Jonathan C Nixon, Nicola B Coates, Lucy Creamer, Paul Hailwood, Sarah Taylor, Gordon J Bhalla, Ashok K Arthritis Res Ther Research Article INTRODUCTION: The pathology of ankylosing spondylitis (AS) suggests that certain cytokines and matrix metalloproteinases (MMPs) might provide useful markers of disease activity. Serum levels of some cytokines and MMPs have been found to be elevated in active disease, but there is a general lack of information about biomarker profiles in AS and how these are related to disease activity and function. The purpose of this study was to investigate whether clinical measures of disease activity and function in AS are associated with particular profiles of circulating cytokines and MMPs. METHODS: Measurement of 30 cytokines, five MMPs and four tissue inhibitors of metalloproteinases was carried out using Luminex(® )technology on a well-characterised population of AS patients (n = 157). The relationship between biomarker levels and measures of disease activity (Bath ankylosing spondylitis disease activity index (BASDAI)), function (Bath ankylosing spondylitis functional index) and global health (Bath ankylosing spondylitis global health) was investigated. Principal component analysis was used to reduce the large number of biomarkers to a smaller set of independent components, which were investigated for their association with clinical measures. Further analyses were carried out using hierarchical clustering, multiple regression or multivariate logistic regression. RESULTS: Principal component analysis identified eight clusters consisting of various combinations of cytokines and MMPs. The strongest association with the BASDAI was found with a component consisting of MMP-8, MMP-9, hepatocyte growth factor and CXCL8, and was independent of C-reactive protein levels. This component was also associated with current smoking. Hierarchical clustering revealed two distinct patient clusters that could be separated on the basis of MMP levels. The high MMP cluster was associated with increased C-reactive protein, the BASDAI and the Bath ankylosing spondylitis functional index. CONCLUSIONS: A profile consisting of high levels of MMP-8, MMP-9, hepatocyte growth factor and CXCL8 is associated with increased disease activity in AS. High MMP levels are also associated with smoking and worse function in AS. BioMed Central 2012 2012-05-28 /pmc/articles/PMC3446508/ /pubmed/22640827 http://dx.doi.org/10.1186/ar3857 Text en Copyright ©2012 Mattey et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Mattey, Derek L Packham, Jonathan C Nixon, Nicola B Coates, Lucy Creamer, Paul Hailwood, Sarah Taylor, Gordon J Bhalla, Ashok K Association of cytokine and matrix metalloproteinase profiles with disease activity and function in ankylosing spondylitis |
title | Association of cytokine and matrix metalloproteinase profiles with disease activity and function in ankylosing spondylitis |
title_full | Association of cytokine and matrix metalloproteinase profiles with disease activity and function in ankylosing spondylitis |
title_fullStr | Association of cytokine and matrix metalloproteinase profiles with disease activity and function in ankylosing spondylitis |
title_full_unstemmed | Association of cytokine and matrix metalloproteinase profiles with disease activity and function in ankylosing spondylitis |
title_short | Association of cytokine and matrix metalloproteinase profiles with disease activity and function in ankylosing spondylitis |
title_sort | association of cytokine and matrix metalloproteinase profiles with disease activity and function in ankylosing spondylitis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3446508/ https://www.ncbi.nlm.nih.gov/pubmed/22640827 http://dx.doi.org/10.1186/ar3857 |
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