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Immune-inflammatory and hypothalamic-pituitary-adrenal axis biomarkers are altered in patients with non-specific low back pain: A systematic review

This systematic review aimed to investigate immune-inflammatory and hypothalamic-pituitary-adrenal (HPA) axis biomarkers in individuals with non-specific low back pain (NSLBP) compared to healthy control. The search was performed in five databases until 4 November 2021. Two reviewers independently c...

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Autores principales: Sanabria-Mazo, Juan P., Colomer-Carbonell, Ariadna, Carmona-Cervelló, Meritxell, Feliu-Soler, Albert, Borràs, Xavier, Grasa, Mar, Esteve, Montserrat, Maes, Michael, Edo, Sílvia, Sanz, Antoni, Luciano, Juan V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9478440/
https://www.ncbi.nlm.nih.gov/pubmed/36119028
http://dx.doi.org/10.3389/fimmu.2022.945513
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author Sanabria-Mazo, Juan P.
Colomer-Carbonell, Ariadna
Carmona-Cervelló, Meritxell
Feliu-Soler, Albert
Borràs, Xavier
Grasa, Mar
Esteve, Montserrat
Maes, Michael
Edo, Sílvia
Sanz, Antoni
Luciano, Juan V.
author_facet Sanabria-Mazo, Juan P.
Colomer-Carbonell, Ariadna
Carmona-Cervelló, Meritxell
Feliu-Soler, Albert
Borràs, Xavier
Grasa, Mar
Esteve, Montserrat
Maes, Michael
Edo, Sílvia
Sanz, Antoni
Luciano, Juan V.
author_sort Sanabria-Mazo, Juan P.
collection PubMed
description This systematic review aimed to investigate immune-inflammatory and hypothalamic-pituitary-adrenal (HPA) axis biomarkers in individuals with non-specific low back pain (NSLBP) compared to healthy control. The search was performed in five databases until 4 November 2021. Two reviewers independently conducted screenings, data extraction, risk of bias, and methodological quality assessment of 14 unique studies. All studies reported the source of the fluid analyzed: nine studies used serum, two used plasma, one used serum and plasma, and two studies used salivary cortisol. We found preliminary and limited evidence (only one study for each biomarker) of increased levels in growth differentiation factor 15 (GDF-15), interleukin-23 (IL-23), transforming growth factor–beta (TGF-β), and soluble tumor necrosis factor receptor 1 (sTNF-R1) in NSLBP. Inconsistent and limited evidence was identified for interleukin-10 (IL-10). Although C-reactive protein (CRP), interleukin-6 (IL-6), and tumor necrosis factor–alpha (TNF-α) levels appear to increase in NSLBP, only one study per each biomarker reported statistically significant differences. Interleukin-1 beta (IL-1β), interleukin-17 (IL-17), interferon gamma (IFN-γ), and high-sensitivity CRP (hsCRP) showed no significant differences. Regarding cortisol, one study showed a significant increase and another a significant decrease. More robust evidence between GDF-15, IL-23, TGF-β, and sTNF-R1 with NSLBP is needed. Moreover, contrary to the findings reported in previous studies, when comparing results exclusively with healthy control, insufficient robust evidence for IL-6, TNF-α, and CRP was found in NSLBP. In addition, cortisol response (HPA-related biomarker) showed a dysregulated functioning in NSLBP, with incongruent evidence regarding its directionality. Therefore, our effort is to find adjusted evidence to conclude which immune-inflammatory and HPA axis biomarkers are altered in NSLBP and how much their levels are affected. SYSTEMATIC REVIEW REGISTRATION: https://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42020176153, identifier CRD42020176153.
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spelling pubmed-94784402022-09-17 Immune-inflammatory and hypothalamic-pituitary-adrenal axis biomarkers are altered in patients with non-specific low back pain: A systematic review Sanabria-Mazo, Juan P. Colomer-Carbonell, Ariadna Carmona-Cervelló, Meritxell Feliu-Soler, Albert Borràs, Xavier Grasa, Mar Esteve, Montserrat Maes, Michael Edo, Sílvia Sanz, Antoni Luciano, Juan V. Front Immunol Immunology This systematic review aimed to investigate immune-inflammatory and hypothalamic-pituitary-adrenal (HPA) axis biomarkers in individuals with non-specific low back pain (NSLBP) compared to healthy control. The search was performed in five databases until 4 November 2021. Two reviewers independently conducted screenings, data extraction, risk of bias, and methodological quality assessment of 14 unique studies. All studies reported the source of the fluid analyzed: nine studies used serum, two used plasma, one used serum and plasma, and two studies used salivary cortisol. We found preliminary and limited evidence (only one study for each biomarker) of increased levels in growth differentiation factor 15 (GDF-15), interleukin-23 (IL-23), transforming growth factor–beta (TGF-β), and soluble tumor necrosis factor receptor 1 (sTNF-R1) in NSLBP. Inconsistent and limited evidence was identified for interleukin-10 (IL-10). Although C-reactive protein (CRP), interleukin-6 (IL-6), and tumor necrosis factor–alpha (TNF-α) levels appear to increase in NSLBP, only one study per each biomarker reported statistically significant differences. Interleukin-1 beta (IL-1β), interleukin-17 (IL-17), interferon gamma (IFN-γ), and high-sensitivity CRP (hsCRP) showed no significant differences. Regarding cortisol, one study showed a significant increase and another a significant decrease. More robust evidence between GDF-15, IL-23, TGF-β, and sTNF-R1 with NSLBP is needed. Moreover, contrary to the findings reported in previous studies, when comparing results exclusively with healthy control, insufficient robust evidence for IL-6, TNF-α, and CRP was found in NSLBP. In addition, cortisol response (HPA-related biomarker) showed a dysregulated functioning in NSLBP, with incongruent evidence regarding its directionality. Therefore, our effort is to find adjusted evidence to conclude which immune-inflammatory and HPA axis biomarkers are altered in NSLBP and how much their levels are affected. SYSTEMATIC REVIEW REGISTRATION: https://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42020176153, identifier CRD42020176153. Frontiers Media S.A. 2022-09-02 /pmc/articles/PMC9478440/ /pubmed/36119028 http://dx.doi.org/10.3389/fimmu.2022.945513 Text en Copyright © 2022 Sanabria-Mazo, Colomer-Carbonell, Carmona-Cervelló, Feliu-Soler, Borràs, Grasa, Esteve, Maes, Edo, Sanz and Luciano https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Sanabria-Mazo, Juan P.
Colomer-Carbonell, Ariadna
Carmona-Cervelló, Meritxell
Feliu-Soler, Albert
Borràs, Xavier
Grasa, Mar
Esteve, Montserrat
Maes, Michael
Edo, Sílvia
Sanz, Antoni
Luciano, Juan V.
Immune-inflammatory and hypothalamic-pituitary-adrenal axis biomarkers are altered in patients with non-specific low back pain: A systematic review
title Immune-inflammatory and hypothalamic-pituitary-adrenal axis biomarkers are altered in patients with non-specific low back pain: A systematic review
title_full Immune-inflammatory and hypothalamic-pituitary-adrenal axis biomarkers are altered in patients with non-specific low back pain: A systematic review
title_fullStr Immune-inflammatory and hypothalamic-pituitary-adrenal axis biomarkers are altered in patients with non-specific low back pain: A systematic review
title_full_unstemmed Immune-inflammatory and hypothalamic-pituitary-adrenal axis biomarkers are altered in patients with non-specific low back pain: A systematic review
title_short Immune-inflammatory and hypothalamic-pituitary-adrenal axis biomarkers are altered in patients with non-specific low back pain: A systematic review
title_sort immune-inflammatory and hypothalamic-pituitary-adrenal axis biomarkers are altered in patients with non-specific low back pain: a systematic review
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9478440/
https://www.ncbi.nlm.nih.gov/pubmed/36119028
http://dx.doi.org/10.3389/fimmu.2022.945513
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