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Macrophage migration inhibitory factor: a potential biomarker for chronic low back pain in patients with Modic changes
BACKGROUND: Low back pain (LBP) is a leading cause of disability worldwide, but the aetiology remains poorly understood. Finding relevant biomarkers may lead to better understanding of disease mechanisms. Patients with vertebral endplate bone marrow lesions visualised on MRI as Modic changes (MCs) h...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8336134/ https://www.ncbi.nlm.nih.gov/pubmed/34344830 http://dx.doi.org/10.1136/rmdopen-2021-001726 |
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author | Gjefsen, Elisabeth Gervin, Kristina Goll, Guro Bråten, Lars Christian Haugli Wigemyr, Monica Aass, Hans Christian D Vigeland, Maria Dehli Schistad, Elina Pedersen, Linda Margareth Pripp, Are Hugo Storheim, Kjersti Selmer, Kaja Kristine Zwart, John Anker |
author_facet | Gjefsen, Elisabeth Gervin, Kristina Goll, Guro Bråten, Lars Christian Haugli Wigemyr, Monica Aass, Hans Christian D Vigeland, Maria Dehli Schistad, Elina Pedersen, Linda Margareth Pripp, Are Hugo Storheim, Kjersti Selmer, Kaja Kristine Zwart, John Anker |
author_sort | Gjefsen, Elisabeth |
collection | PubMed |
description | BACKGROUND: Low back pain (LBP) is a leading cause of disability worldwide, but the aetiology remains poorly understood. Finding relevant biomarkers may lead to better understanding of disease mechanisms. Patients with vertebral endplate bone marrow lesions visualised on MRI as Modic changes (MCs) have been proposed as a distinct LBP phenotype, and inflammatory mediators may be involved in the development of MCs. OBJECTIVES: To identify possible serum biomarkers for LBP in patients with MCs. METHODS: In this case control study serum levels of 40 cytokines were compared between patients with LBP and MC type 1 (n=46) or type 2 (n=37) and healthy controls (n=50). RESULTS: Analyses identified significantly higher levels of six out of 40 cytokines in the MC type 1 group (MC1), and five in the MC type 2 group (MC2) compared with healthy controls. Six cytokines were moderately correlated with pain. Principal component analyses revealed clustering and separation of patients with LBP and controls, capturing 40.8% of the total variance, with 10 cytokines contributing to the separation. Macrophage migration inhibitory factor (MIF) alone accounted for 92% of the total contribution. Further, receiver operating characteristics analysis revealed that MIF showed an acceptable ability to distinguish between patients and controls (area under the curve=0.79). CONCLUSIONS: These results suggest that cytokines may play a role in LBP with MCs. The clinical significance of the findings is unknown. MIF strongly contributed to clustering of patients with LBP with MCs and controls, and might be a biomarker for MCs. Ultimately, these results may guide future research on novel treatments for this patient group. |
format | Online Article Text |
id | pubmed-8336134 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-83361342021-08-20 Macrophage migration inhibitory factor: a potential biomarker for chronic low back pain in patients with Modic changes Gjefsen, Elisabeth Gervin, Kristina Goll, Guro Bråten, Lars Christian Haugli Wigemyr, Monica Aass, Hans Christian D Vigeland, Maria Dehli Schistad, Elina Pedersen, Linda Margareth Pripp, Are Hugo Storheim, Kjersti Selmer, Kaja Kristine Zwart, John Anker RMD Open Spine BACKGROUND: Low back pain (LBP) is a leading cause of disability worldwide, but the aetiology remains poorly understood. Finding relevant biomarkers may lead to better understanding of disease mechanisms. Patients with vertebral endplate bone marrow lesions visualised on MRI as Modic changes (MCs) have been proposed as a distinct LBP phenotype, and inflammatory mediators may be involved in the development of MCs. OBJECTIVES: To identify possible serum biomarkers for LBP in patients with MCs. METHODS: In this case control study serum levels of 40 cytokines were compared between patients with LBP and MC type 1 (n=46) or type 2 (n=37) and healthy controls (n=50). RESULTS: Analyses identified significantly higher levels of six out of 40 cytokines in the MC type 1 group (MC1), and five in the MC type 2 group (MC2) compared with healthy controls. Six cytokines were moderately correlated with pain. Principal component analyses revealed clustering and separation of patients with LBP and controls, capturing 40.8% of the total variance, with 10 cytokines contributing to the separation. Macrophage migration inhibitory factor (MIF) alone accounted for 92% of the total contribution. Further, receiver operating characteristics analysis revealed that MIF showed an acceptable ability to distinguish between patients and controls (area under the curve=0.79). CONCLUSIONS: These results suggest that cytokines may play a role in LBP with MCs. The clinical significance of the findings is unknown. MIF strongly contributed to clustering of patients with LBP with MCs and controls, and might be a biomarker for MCs. Ultimately, these results may guide future research on novel treatments for this patient group. BMJ Publishing Group 2021-08-03 /pmc/articles/PMC8336134/ /pubmed/34344830 http://dx.doi.org/10.1136/rmdopen-2021-001726 Text en © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Spine Gjefsen, Elisabeth Gervin, Kristina Goll, Guro Bråten, Lars Christian Haugli Wigemyr, Monica Aass, Hans Christian D Vigeland, Maria Dehli Schistad, Elina Pedersen, Linda Margareth Pripp, Are Hugo Storheim, Kjersti Selmer, Kaja Kristine Zwart, John Anker Macrophage migration inhibitory factor: a potential biomarker for chronic low back pain in patients with Modic changes |
title | Macrophage migration inhibitory factor: a potential biomarker for chronic low back pain in patients with Modic changes |
title_full | Macrophage migration inhibitory factor: a potential biomarker for chronic low back pain in patients with Modic changes |
title_fullStr | Macrophage migration inhibitory factor: a potential biomarker for chronic low back pain in patients with Modic changes |
title_full_unstemmed | Macrophage migration inhibitory factor: a potential biomarker for chronic low back pain in patients with Modic changes |
title_short | Macrophage migration inhibitory factor: a potential biomarker for chronic low back pain in patients with Modic changes |
title_sort | macrophage migration inhibitory factor: a potential biomarker for chronic low back pain in patients with modic changes |
topic | Spine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8336134/ https://www.ncbi.nlm.nih.gov/pubmed/34344830 http://dx.doi.org/10.1136/rmdopen-2021-001726 |
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