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Serum biomarkers in people with chronic low back pain and Modic 1 changes: a case-control study

We aimed to compare serum biomarkers of inflammation, redox status and cartilage degradation between chronic low back pain (cLBP) patients with and without Modic 1 changes. We used a convenience sample of patients recruited from a single center, case-control study, conducted in a tertiary care cente...

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Autores principales: Boisson, Margaux, Borderie, Didier, Henrotin, Yves, Teboul-Coré, Stéphanie, Lefèvre-Colau, Marie-Martine, Rannou, François, Nguyen, Christelle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6620434/
https://www.ncbi.nlm.nih.gov/pubmed/31292506
http://dx.doi.org/10.1038/s41598-019-46508-x
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author Boisson, Margaux
Borderie, Didier
Henrotin, Yves
Teboul-Coré, Stéphanie
Lefèvre-Colau, Marie-Martine
Rannou, François
Nguyen, Christelle
author_facet Boisson, Margaux
Borderie, Didier
Henrotin, Yves
Teboul-Coré, Stéphanie
Lefèvre-Colau, Marie-Martine
Rannou, François
Nguyen, Christelle
author_sort Boisson, Margaux
collection PubMed
description We aimed to compare serum biomarkers of inflammation, redox status and cartilage degradation between chronic low back pain (cLBP) patients with and without Modic 1 changes. We used a convenience sample of patients recruited from a single center, case-control study, conducted in a tertiary care center. From December, 2014 to May, 2016, 2,292 patients were consecutively screened, 34 met inclusion criteria and were prospectively enrolled in the present study. Cases (n = 13) were defined as patients with Modic 1 changes detected on MRI and controls (n = 21) as cLBP patients without (Modic 0). To assess serum biomarkers of inflammation, redox status and cartilage degradation, fasting serum samples were collected in a standardized manner and analyzed by immunoassays and spectrophotometry. Mean (95% CI) age was 44.1 (40.0–48.1) years and mean LBP duration was 72.5 (53.0–91.9) months. Serum biomarkers of inflammation (IL-1β, IL-6, IL-8 and TNF-α), redox status (total thiols, advanced oxidation protein products and carbonyl groups) and cartilage degradation (Coll2-1 and Coll2-1NO(2)) did not differ between cLBP patients with and without Modic 1 changes. In summary, we did not find any differences in serum biomarkers between cLBP patients with and without Modic 1 changes. Interpretation is limited by convenience sampling and small sample size.
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spelling pubmed-66204342019-07-19 Serum biomarkers in people with chronic low back pain and Modic 1 changes: a case-control study Boisson, Margaux Borderie, Didier Henrotin, Yves Teboul-Coré, Stéphanie Lefèvre-Colau, Marie-Martine Rannou, François Nguyen, Christelle Sci Rep Article We aimed to compare serum biomarkers of inflammation, redox status and cartilage degradation between chronic low back pain (cLBP) patients with and without Modic 1 changes. We used a convenience sample of patients recruited from a single center, case-control study, conducted in a tertiary care center. From December, 2014 to May, 2016, 2,292 patients were consecutively screened, 34 met inclusion criteria and were prospectively enrolled in the present study. Cases (n = 13) were defined as patients with Modic 1 changes detected on MRI and controls (n = 21) as cLBP patients without (Modic 0). To assess serum biomarkers of inflammation, redox status and cartilage degradation, fasting serum samples were collected in a standardized manner and analyzed by immunoassays and spectrophotometry. Mean (95% CI) age was 44.1 (40.0–48.1) years and mean LBP duration was 72.5 (53.0–91.9) months. Serum biomarkers of inflammation (IL-1β, IL-6, IL-8 and TNF-α), redox status (total thiols, advanced oxidation protein products and carbonyl groups) and cartilage degradation (Coll2-1 and Coll2-1NO(2)) did not differ between cLBP patients with and without Modic 1 changes. In summary, we did not find any differences in serum biomarkers between cLBP patients with and without Modic 1 changes. Interpretation is limited by convenience sampling and small sample size. Nature Publishing Group UK 2019-07-10 /pmc/articles/PMC6620434/ /pubmed/31292506 http://dx.doi.org/10.1038/s41598-019-46508-x Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Boisson, Margaux
Borderie, Didier
Henrotin, Yves
Teboul-Coré, Stéphanie
Lefèvre-Colau, Marie-Martine
Rannou, François
Nguyen, Christelle
Serum biomarkers in people with chronic low back pain and Modic 1 changes: a case-control study
title Serum biomarkers in people with chronic low back pain and Modic 1 changes: a case-control study
title_full Serum biomarkers in people with chronic low back pain and Modic 1 changes: a case-control study
title_fullStr Serum biomarkers in people with chronic low back pain and Modic 1 changes: a case-control study
title_full_unstemmed Serum biomarkers in people with chronic low back pain and Modic 1 changes: a case-control study
title_short Serum biomarkers in people with chronic low back pain and Modic 1 changes: a case-control study
title_sort serum biomarkers in people with chronic low back pain and modic 1 changes: a case-control study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6620434/
https://www.ncbi.nlm.nih.gov/pubmed/31292506
http://dx.doi.org/10.1038/s41598-019-46508-x
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