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The predictive value of serum S100A9 and response to etanercept is not confirmed in a large UK rheumatoid arthritis cohort
Objective. The aim was to correlate protein concentrations of S100A9 in pretreatment serum samples with response to the tumour-necrosis factor (TNF) inhibitor drugs etanercept in a large UK replication cohort. Methods. Pretreatment serum samples from patients with RA (n = 236) about to commence trea...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5445600/ https://www.ncbi.nlm.nih.gov/pubmed/28096457 http://dx.doi.org/10.1093/rheumatology/kew387 |
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author | Smith, Samantha Louise Plant, Darren Eyre, Stephen Hyrich, Kimme Morgan, Ann W. Wilson, Anthony G. Isaacs, John D. Barton, Anne |
author_facet | Smith, Samantha Louise Plant, Darren Eyre, Stephen Hyrich, Kimme Morgan, Ann W. Wilson, Anthony G. Isaacs, John D. Barton, Anne |
author_sort | Smith, Samantha Louise |
collection | PubMed |
description | Objective. The aim was to correlate protein concentrations of S100A9 in pretreatment serum samples with response to the tumour-necrosis factor (TNF) inhibitor drugs etanercept in a large UK replication cohort. Methods. Pretreatment serum samples from patients with RA (n = 236) about to commence treatment with etanercept had S100A9 serum concentration measured using an ELISA. Following the experimental procedure, S100A9 concentrations were analysed with respect to EULAR response. Results. No evidence of association between S100A9 concentration and EULAR response to the TNF-inhibitor biologic drug etanercept was observed following multinomial logistic regression analysis (non-responder vs moderate responder, P = 0.957; and non-responder vs good responder, P = 0.316). Furthermore, no significant associations were observed when correlating pretreatment S100A9 concentrations with clinical parameters of disease activity (P > 0.05). Conclusion. In the largest replication cohort conducted to date, no evidence for association was observed to support the use of S100A9 as a clinical biomarker predictive of response to the TNF-inhibitor biologic drug etanercept. |
format | Online Article Text |
id | pubmed-5445600 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-54456002017-05-31 The predictive value of serum S100A9 and response to etanercept is not confirmed in a large UK rheumatoid arthritis cohort Smith, Samantha Louise Plant, Darren Eyre, Stephen Hyrich, Kimme Morgan, Ann W. Wilson, Anthony G. Isaacs, John D. Barton, Anne Rheumatology (Oxford) Basic and Translational Science Objective. The aim was to correlate protein concentrations of S100A9 in pretreatment serum samples with response to the tumour-necrosis factor (TNF) inhibitor drugs etanercept in a large UK replication cohort. Methods. Pretreatment serum samples from patients with RA (n = 236) about to commence treatment with etanercept had S100A9 serum concentration measured using an ELISA. Following the experimental procedure, S100A9 concentrations were analysed with respect to EULAR response. Results. No evidence of association between S100A9 concentration and EULAR response to the TNF-inhibitor biologic drug etanercept was observed following multinomial logistic regression analysis (non-responder vs moderate responder, P = 0.957; and non-responder vs good responder, P = 0.316). Furthermore, no significant associations were observed when correlating pretreatment S100A9 concentrations with clinical parameters of disease activity (P > 0.05). Conclusion. In the largest replication cohort conducted to date, no evidence for association was observed to support the use of S100A9 as a clinical biomarker predictive of response to the TNF-inhibitor biologic drug etanercept. Oxford University Press 2017-06 2017-01-16 /pmc/articles/PMC5445600/ /pubmed/28096457 http://dx.doi.org/10.1093/rheumatology/kew387 Text en © The Author 2017. Published by Oxford University Press on behalf of the British Society for Rheumatology. 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Basic and Translational Science Smith, Samantha Louise Plant, Darren Eyre, Stephen Hyrich, Kimme Morgan, Ann W. Wilson, Anthony G. Isaacs, John D. Barton, Anne The predictive value of serum S100A9 and response to etanercept is not confirmed in a large UK rheumatoid arthritis cohort |
title | The predictive value of serum S100A9 and response to etanercept is not confirmed in a large UK rheumatoid arthritis cohort |
title_full | The predictive value of serum S100A9 and response to etanercept is not confirmed in a large UK rheumatoid arthritis cohort |
title_fullStr | The predictive value of serum S100A9 and response to etanercept is not confirmed in a large UK rheumatoid arthritis cohort |
title_full_unstemmed | The predictive value of serum S100A9 and response to etanercept is not confirmed in a large UK rheumatoid arthritis cohort |
title_short | The predictive value of serum S100A9 and response to etanercept is not confirmed in a large UK rheumatoid arthritis cohort |
title_sort | predictive value of serum s100a9 and response to etanercept is not confirmed in a large uk rheumatoid arthritis cohort |
topic | Basic and Translational Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5445600/ https://www.ncbi.nlm.nih.gov/pubmed/28096457 http://dx.doi.org/10.1093/rheumatology/kew387 |
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