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Unexpectedly decreased plasma cytokines in patients with chronic back pain

INTRODUCTION: Chronic back pain is one of the most important socioeconomic problems that affects the global population. Elevated levels of inflammatory mediators, such as cytokines, have been correlated with pain, but their role in chronic back pain remains unclear. The effectiveness of anti-inflamm...

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Autores principales: Capossela, Simona, Pavlicek, David, Bertolo, Alessandro, Landmann, Gunther, Stoyanov, Jivko V
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6016579/
https://www.ncbi.nlm.nih.gov/pubmed/29950891
http://dx.doi.org/10.2147/JPR.S153872
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author Capossela, Simona
Pavlicek, David
Bertolo, Alessandro
Landmann, Gunther
Stoyanov, Jivko V
author_facet Capossela, Simona
Pavlicek, David
Bertolo, Alessandro
Landmann, Gunther
Stoyanov, Jivko V
author_sort Capossela, Simona
collection PubMed
description INTRODUCTION: Chronic back pain is one of the most important socioeconomic problems that affects the global population. Elevated levels of inflammatory mediators, such as cytokines, have been correlated with pain, but their role in chronic back pain remains unclear. The effectiveness of anti-inflammatory drugs seems to be limited for chronic back pain. The authors wanted to investigate the levels of inflammatory mediators in long-term medically treated patients with persistent chronic back pain. METHODS: Cytokine plasma levels of patients with chronic back pain (n=23), compared to pain-free healthy controls (n=30), were investigated by immunoassay. Patients with chronic back pain were exposed to long-term conservative medical therapy with physiotherapy and anti-inflammatories, also combined with antidepressants and/or muscle-relaxants. RESULTS: The patients with chronic back pain expressed lower levels of the chemokines MCP1, CCL5, and CXCL6 compared to pain-free healthy controls. Significantly lower concentrations of the anti-inflammatory cytokines, interleukin (IL)-4 and granulocyte-colony stimulating factor were also found. Interestingly, levels of proinflammatory cytokines (IL-2, IL-6, IL-1β, tumor necrosis factor alpha), IL-10, granulocyte-macrophage colony-stimulating factor, and stromal cell-derived factor 1 alpha showed no significant differences between both groups. CONCLUSION: This decrease of inflammatory mediators in medically treated patients with chronic back pain is of unclear origin and might be either a long-term side effect of medical therapy or related to chronic pain. Further longitudinal research is necessary to elucidate the underlying cause of these findings.
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spelling pubmed-60165792018-06-27 Unexpectedly decreased plasma cytokines in patients with chronic back pain Capossela, Simona Pavlicek, David Bertolo, Alessandro Landmann, Gunther Stoyanov, Jivko V J Pain Res Original Research INTRODUCTION: Chronic back pain is one of the most important socioeconomic problems that affects the global population. Elevated levels of inflammatory mediators, such as cytokines, have been correlated with pain, but their role in chronic back pain remains unclear. The effectiveness of anti-inflammatory drugs seems to be limited for chronic back pain. The authors wanted to investigate the levels of inflammatory mediators in long-term medically treated patients with persistent chronic back pain. METHODS: Cytokine plasma levels of patients with chronic back pain (n=23), compared to pain-free healthy controls (n=30), were investigated by immunoassay. Patients with chronic back pain were exposed to long-term conservative medical therapy with physiotherapy and anti-inflammatories, also combined with antidepressants and/or muscle-relaxants. RESULTS: The patients with chronic back pain expressed lower levels of the chemokines MCP1, CCL5, and CXCL6 compared to pain-free healthy controls. Significantly lower concentrations of the anti-inflammatory cytokines, interleukin (IL)-4 and granulocyte-colony stimulating factor were also found. Interestingly, levels of proinflammatory cytokines (IL-2, IL-6, IL-1β, tumor necrosis factor alpha), IL-10, granulocyte-macrophage colony-stimulating factor, and stromal cell-derived factor 1 alpha showed no significant differences between both groups. CONCLUSION: This decrease of inflammatory mediators in medically treated patients with chronic back pain is of unclear origin and might be either a long-term side effect of medical therapy or related to chronic pain. Further longitudinal research is necessary to elucidate the underlying cause of these findings. Dove Medical Press 2018-06-21 /pmc/articles/PMC6016579/ /pubmed/29950891 http://dx.doi.org/10.2147/JPR.S153872 Text en © 2018 Capossela et al. This work is published by Dove Medical Press Limite The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Capossela, Simona
Pavlicek, David
Bertolo, Alessandro
Landmann, Gunther
Stoyanov, Jivko V
Unexpectedly decreased plasma cytokines in patients with chronic back pain
title Unexpectedly decreased plasma cytokines in patients with chronic back pain
title_full Unexpectedly decreased plasma cytokines in patients with chronic back pain
title_fullStr Unexpectedly decreased plasma cytokines in patients with chronic back pain
title_full_unstemmed Unexpectedly decreased plasma cytokines in patients with chronic back pain
title_short Unexpectedly decreased plasma cytokines in patients with chronic back pain
title_sort unexpectedly decreased plasma cytokines in patients with chronic back pain
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6016579/
https://www.ncbi.nlm.nih.gov/pubmed/29950891
http://dx.doi.org/10.2147/JPR.S153872
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