Cargando…

Serum levels of 14-3-3η protein supplement C-reactive protein and rheumatoid arthritis-associated antibodies to predict clinical and radiographic outcomes in a prospective cohort of patients with recent-onset inflammatory polyarthritis

BACKGROUND: Age, C-Reactive Protein (CRP) and autoantibodies (Abs) are associated with worse prognosis in patients with recent-onset inflammatory polyarthritis (EPA). Serum 14-3-3η protein is a joint-derived biomarker that up-regulates cytokines and enzymes that perpetuate local and systemic inflamm...

Descripción completa

Detalles Bibliográficos
Autores principales: Carrier, Nathalie, Marotta, Anthony, de Brum-Fernandes, Artur J., Liang, Patrick, Masetto, Ariel, Ménard, Henri A., Maksymowych, Walter P., Boire, Gilles
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4736641/
https://www.ncbi.nlm.nih.gov/pubmed/26832367
http://dx.doi.org/10.1186/s13075-016-0935-z
_version_ 1782413324209618944
author Carrier, Nathalie
Marotta, Anthony
de Brum-Fernandes, Artur J.
Liang, Patrick
Masetto, Ariel
Ménard, Henri A.
Maksymowych, Walter P.
Boire, Gilles
author_facet Carrier, Nathalie
Marotta, Anthony
de Brum-Fernandes, Artur J.
Liang, Patrick
Masetto, Ariel
Ménard, Henri A.
Maksymowych, Walter P.
Boire, Gilles
author_sort Carrier, Nathalie
collection PubMed
description BACKGROUND: Age, C-Reactive Protein (CRP) and autoantibodies (Abs) are associated with worse prognosis in patients with recent-onset inflammatory polyarthritis (EPA). Serum 14-3-3η protein is a joint-derived biomarker that up-regulates cytokines and enzymes that perpetuate local and systemic inflammation and may contribute to joint damage. Our objective was to evaluate, over a 5-year prospective period of observation, the additional prognostic potential of serum 14-3-3η protein in EPA patients. METHODS: Clinical variables, serum and radiographs (scored according to the Sharp/van der Heijde (SvH) method) were collected serially. Relationships between serum 14-3-3η protein and other biomarkers were computed with Spearman correlations. Outcomes were Simple Disease Activity Index (SDAI) scores and joint damage progression: ΔSvH for SvH score and ΔErosion for its Erosive component. The additional predictive contribution of 14-3-3η was defined using generalized estimating equations (GEE) and generalized linear mixed models (GLMM). RESULTS: Among 331 patients, baseline 14-3-3η was ≥0.19 and ≥0.50 ng/ml in 153 (46.2 %) and 119 (36.0 %), respectively; CRP was >8.0 mg/L in 207 (62.5 %), and at least one Ab (Rheumatoid Factor, anti-CCP2 or anti-Sa/citrullinated vimentin) was positive in 170 (51.5 %). Elevated 14-3-3η levels moderately correlated with positive Abs, but not with elevated CRP. Baseline 14-3-3η ≥0.19 ng/ml was associated with more radiographic progression over 5 years. The optimal levels of baseline 14-3-3η to predict radiographic progression was defined by ROC curves at 0.50 ng/ml. Levels of 14-3-3η ≥0.50 ng/ml at baseline were associated with lower likelihoods of ever reaching SDAI remission (RR 0.79 (95 % CI 0.64–0.98), p = 0.03) and higher subsequent progression of Total and Erosion SvH scores. Elevated levels of 14-3-3η during follow-up also predicted higher subsequent progression, even in patients in SDAI remission. Decreases of 14-3-3η levels by at least 0.76 ng/ml and reversion to negative during follow-up associated with less subsequent radiographic progression. In multivariate models, elevated 14-3-3η interacted with positive Abs, elevated CRP and older age to predict subsequent radiographic progression. CONCLUSIONS: Levels of 14-3-3η protein ≥0.50 ng/ml predict poorer clinical and radiographic outcomes in EPA, both at baseline and after initiation of treatment, even in SDAI remitters. 14-3-3η, CRP, age and Abs represent independent predictors of subsequent joint damage. TRIAL REGISTRATION: ClinicalTrials.gov ID: NCT00512239. Registered August 6, 2007. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13075-016-0935-z) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-4736641
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-47366412016-02-03 Serum levels of 14-3-3η protein supplement C-reactive protein and rheumatoid arthritis-associated antibodies to predict clinical and radiographic outcomes in a prospective cohort of patients with recent-onset inflammatory polyarthritis Carrier, Nathalie Marotta, Anthony de Brum-Fernandes, Artur J. Liang, Patrick Masetto, Ariel Ménard, Henri A. Maksymowych, Walter P. Boire, Gilles Arthritis Res Ther Research Article BACKGROUND: Age, C-Reactive Protein (CRP) and autoantibodies (Abs) are associated with worse prognosis in patients with recent-onset inflammatory polyarthritis (EPA). Serum 14-3-3η protein is a joint-derived biomarker that up-regulates cytokines and enzymes that perpetuate local and systemic inflammation and may contribute to joint damage. Our objective was to evaluate, over a 5-year prospective period of observation, the additional prognostic potential of serum 14-3-3η protein in EPA patients. METHODS: Clinical variables, serum and radiographs (scored according to the Sharp/van der Heijde (SvH) method) were collected serially. Relationships between serum 14-3-3η protein and other biomarkers were computed with Spearman correlations. Outcomes were Simple Disease Activity Index (SDAI) scores and joint damage progression: ΔSvH for SvH score and ΔErosion for its Erosive component. The additional predictive contribution of 14-3-3η was defined using generalized estimating equations (GEE) and generalized linear mixed models (GLMM). RESULTS: Among 331 patients, baseline 14-3-3η was ≥0.19 and ≥0.50 ng/ml in 153 (46.2 %) and 119 (36.0 %), respectively; CRP was >8.0 mg/L in 207 (62.5 %), and at least one Ab (Rheumatoid Factor, anti-CCP2 or anti-Sa/citrullinated vimentin) was positive in 170 (51.5 %). Elevated 14-3-3η levels moderately correlated with positive Abs, but not with elevated CRP. Baseline 14-3-3η ≥0.19 ng/ml was associated with more radiographic progression over 5 years. The optimal levels of baseline 14-3-3η to predict radiographic progression was defined by ROC curves at 0.50 ng/ml. Levels of 14-3-3η ≥0.50 ng/ml at baseline were associated with lower likelihoods of ever reaching SDAI remission (RR 0.79 (95 % CI 0.64–0.98), p = 0.03) and higher subsequent progression of Total and Erosion SvH scores. Elevated levels of 14-3-3η during follow-up also predicted higher subsequent progression, even in patients in SDAI remission. Decreases of 14-3-3η levels by at least 0.76 ng/ml and reversion to negative during follow-up associated with less subsequent radiographic progression. In multivariate models, elevated 14-3-3η interacted with positive Abs, elevated CRP and older age to predict subsequent radiographic progression. CONCLUSIONS: Levels of 14-3-3η protein ≥0.50 ng/ml predict poorer clinical and radiographic outcomes in EPA, both at baseline and after initiation of treatment, even in SDAI remitters. 14-3-3η, CRP, age and Abs represent independent predictors of subsequent joint damage. TRIAL REGISTRATION: ClinicalTrials.gov ID: NCT00512239. Registered August 6, 2007. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13075-016-0935-z) contains supplementary material, which is available to authorized users. BioMed Central 2016-02-01 2016 /pmc/articles/PMC4736641/ /pubmed/26832367 http://dx.doi.org/10.1186/s13075-016-0935-z Text en © Carrier et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Carrier, Nathalie
Marotta, Anthony
de Brum-Fernandes, Artur J.
Liang, Patrick
Masetto, Ariel
Ménard, Henri A.
Maksymowych, Walter P.
Boire, Gilles
Serum levels of 14-3-3η protein supplement C-reactive protein and rheumatoid arthritis-associated antibodies to predict clinical and radiographic outcomes in a prospective cohort of patients with recent-onset inflammatory polyarthritis
title Serum levels of 14-3-3η protein supplement C-reactive protein and rheumatoid arthritis-associated antibodies to predict clinical and radiographic outcomes in a prospective cohort of patients with recent-onset inflammatory polyarthritis
title_full Serum levels of 14-3-3η protein supplement C-reactive protein and rheumatoid arthritis-associated antibodies to predict clinical and radiographic outcomes in a prospective cohort of patients with recent-onset inflammatory polyarthritis
title_fullStr Serum levels of 14-3-3η protein supplement C-reactive protein and rheumatoid arthritis-associated antibodies to predict clinical and radiographic outcomes in a prospective cohort of patients with recent-onset inflammatory polyarthritis
title_full_unstemmed Serum levels of 14-3-3η protein supplement C-reactive protein and rheumatoid arthritis-associated antibodies to predict clinical and radiographic outcomes in a prospective cohort of patients with recent-onset inflammatory polyarthritis
title_short Serum levels of 14-3-3η protein supplement C-reactive protein and rheumatoid arthritis-associated antibodies to predict clinical and radiographic outcomes in a prospective cohort of patients with recent-onset inflammatory polyarthritis
title_sort serum levels of 14-3-3η protein supplement c-reactive protein and rheumatoid arthritis-associated antibodies to predict clinical and radiographic outcomes in a prospective cohort of patients with recent-onset inflammatory polyarthritis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4736641/
https://www.ncbi.nlm.nih.gov/pubmed/26832367
http://dx.doi.org/10.1186/s13075-016-0935-z
work_keys_str_mv AT carriernathalie serumlevelsof1433ēproteinsupplementcreactiveproteinandrheumatoidarthritisassociatedantibodiestopredictclinicalandradiographicoutcomesinaprospectivecohortofpatientswithrecentonsetinflammatorypolyarthritis
AT marottaanthony serumlevelsof1433ēproteinsupplementcreactiveproteinandrheumatoidarthritisassociatedantibodiestopredictclinicalandradiographicoutcomesinaprospectivecohortofpatientswithrecentonsetinflammatorypolyarthritis
AT debrumfernandesarturj serumlevelsof1433ēproteinsupplementcreactiveproteinandrheumatoidarthritisassociatedantibodiestopredictclinicalandradiographicoutcomesinaprospectivecohortofpatientswithrecentonsetinflammatorypolyarthritis
AT liangpatrick serumlevelsof1433ēproteinsupplementcreactiveproteinandrheumatoidarthritisassociatedantibodiestopredictclinicalandradiographicoutcomesinaprospectivecohortofpatientswithrecentonsetinflammatorypolyarthritis
AT masettoariel serumlevelsof1433ēproteinsupplementcreactiveproteinandrheumatoidarthritisassociatedantibodiestopredictclinicalandradiographicoutcomesinaprospectivecohortofpatientswithrecentonsetinflammatorypolyarthritis
AT menardhenria serumlevelsof1433ēproteinsupplementcreactiveproteinandrheumatoidarthritisassociatedantibodiestopredictclinicalandradiographicoutcomesinaprospectivecohortofpatientswithrecentonsetinflammatorypolyarthritis
AT maksymowychwalterp serumlevelsof1433ēproteinsupplementcreactiveproteinandrheumatoidarthritisassociatedantibodiestopredictclinicalandradiographicoutcomesinaprospectivecohortofpatientswithrecentonsetinflammatorypolyarthritis
AT boiregilles serumlevelsof1433ēproteinsupplementcreactiveproteinandrheumatoidarthritisassociatedantibodiestopredictclinicalandradiographicoutcomesinaprospectivecohortofpatientswithrecentonsetinflammatorypolyarthritis