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Serum adiponectin as a predictor of laboratory response to anti-TNF-α therapy in rheumatoid arthritis

INTRODUCTION: While adiponectin is typically viewed as an anti-inflammatory mediator, such an activity of adiponectin in rheumatoid arthritis (RA) is not so obvious. In the present study we examined whether serum levels of adiponectin reflect the clinical phenotype of RA patients and/or correlate wi...

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Autores principales: Sikorska, Dorota, Rutkowski, Rafał, Łuczak, Joanna, Samborski, Włodzimierz, Witowski, Janusz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Polish Society of Experimental and Clinical Immunology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6305609/
https://www.ncbi.nlm.nih.gov/pubmed/30588174
http://dx.doi.org/10.5114/ceji.2018.80048
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author Sikorska, Dorota
Rutkowski, Rafał
Łuczak, Joanna
Samborski, Włodzimierz
Witowski, Janusz
author_facet Sikorska, Dorota
Rutkowski, Rafał
Łuczak, Joanna
Samborski, Włodzimierz
Witowski, Janusz
author_sort Sikorska, Dorota
collection PubMed
description INTRODUCTION: While adiponectin is typically viewed as an anti-inflammatory mediator, such an activity of adiponectin in rheumatoid arthritis (RA) is not so obvious. In the present study we examined whether serum levels of adiponectin reflect the clinical phenotype of RA patients and/or correlate with severity of the disease and the response to anti-TNF-α therapy. MATERIAL AND METHODS: Twenty-one female RA patients qualified to receive anti-TNF-α treatment were prospectively assessed before and after 12 weeks of therapy. Patients underwent full clinical and biochemical assessment. Disease activity was assessed by the Modified Disease Activity Scores (DAS28). Serum concentrations of adiponectin were measured with an immunoassay. The individuals were divided into two subgroups according to whether their baseline serum adiponectin was below or above the median value. The subgroups did not differ in basic demographic, anthropometric, and clinical parameters. RESULTS: Anti-TNF-α treatment resulted in a significant clinical (DAS28) improvement in patients from both subgroups, but no significant differences between basal and post-treatment serum adiponectin concentrations were observed. However, patients with higher baseline adiponectin experienced a significant and more pronounced improvement in laboratory parameters of inflammation (ESR, CRP, neutrophil count, neutrophil-to-lymphocyte ratio). CONCLUSIONS: It is possible that adiponectin exerts systemic anti-inflammatory effects independently of the local activity of RA.
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spelling pubmed-63056092018-12-26 Serum adiponectin as a predictor of laboratory response to anti-TNF-α therapy in rheumatoid arthritis Sikorska, Dorota Rutkowski, Rafał Łuczak, Joanna Samborski, Włodzimierz Witowski, Janusz Cent Eur J Immunol Clinical Immunology INTRODUCTION: While adiponectin is typically viewed as an anti-inflammatory mediator, such an activity of adiponectin in rheumatoid arthritis (RA) is not so obvious. In the present study we examined whether serum levels of adiponectin reflect the clinical phenotype of RA patients and/or correlate with severity of the disease and the response to anti-TNF-α therapy. MATERIAL AND METHODS: Twenty-one female RA patients qualified to receive anti-TNF-α treatment were prospectively assessed before and after 12 weeks of therapy. Patients underwent full clinical and biochemical assessment. Disease activity was assessed by the Modified Disease Activity Scores (DAS28). Serum concentrations of adiponectin were measured with an immunoassay. The individuals were divided into two subgroups according to whether their baseline serum adiponectin was below or above the median value. The subgroups did not differ in basic demographic, anthropometric, and clinical parameters. RESULTS: Anti-TNF-α treatment resulted in a significant clinical (DAS28) improvement in patients from both subgroups, but no significant differences between basal and post-treatment serum adiponectin concentrations were observed. However, patients with higher baseline adiponectin experienced a significant and more pronounced improvement in laboratory parameters of inflammation (ESR, CRP, neutrophil count, neutrophil-to-lymphocyte ratio). CONCLUSIONS: It is possible that adiponectin exerts systemic anti-inflammatory effects independently of the local activity of RA. Polish Society of Experimental and Clinical Immunology 2018-10-30 2018 /pmc/articles/PMC6305609/ /pubmed/30588174 http://dx.doi.org/10.5114/ceji.2018.80048 Text en Copyright: © 2018 Polish Society of Experimental and Clinical Immunology http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle Clinical Immunology
Sikorska, Dorota
Rutkowski, Rafał
Łuczak, Joanna
Samborski, Włodzimierz
Witowski, Janusz
Serum adiponectin as a predictor of laboratory response to anti-TNF-α therapy in rheumatoid arthritis
title Serum adiponectin as a predictor of laboratory response to anti-TNF-α therapy in rheumatoid arthritis
title_full Serum adiponectin as a predictor of laboratory response to anti-TNF-α therapy in rheumatoid arthritis
title_fullStr Serum adiponectin as a predictor of laboratory response to anti-TNF-α therapy in rheumatoid arthritis
title_full_unstemmed Serum adiponectin as a predictor of laboratory response to anti-TNF-α therapy in rheumatoid arthritis
title_short Serum adiponectin as a predictor of laboratory response to anti-TNF-α therapy in rheumatoid arthritis
title_sort serum adiponectin as a predictor of laboratory response to anti-tnf-α therapy in rheumatoid arthritis
topic Clinical Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6305609/
https://www.ncbi.nlm.nih.gov/pubmed/30588174
http://dx.doi.org/10.5114/ceji.2018.80048
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