Startseite The serum concentrations of leptin and MCP-1 independently predict low back pain duration
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The serum concentrations of leptin and MCP-1 independently predict low back pain duration

  • Giuseppe Lippi ORCID logo EMAIL logo , Concetta Dagostino , Ruggero Buonocore , Rosalia Aloe , Chiara Bonaguri , Guido Fanelli und Massimo Allegri
Veröffentlicht/Copyright: 11. Januar 2017
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Abstract

Background:

Low back pain (LBP) is a very frequent condition, affecting most people at some point throughout their life. This cross-sectional study was aimed to investigate a selected panel of cytokines and inflammatory biomarkers in patients with or without LBP.

Methods:

The study population consisted of 104 patients diagnosed with LBP (52 non-persistent and 52 persistent) and 52 healthy subjects with no LBP. Blood samples were collected for assessment of adiponectin, leptin, monocyte chemoattractant protein-1 (MCP-1) and C reactive protein (CRP). The duration of LBP was categorized as “no pain”, “non-persistent LBP” and “persistent LBP”.

Results:

Higher values of CRP and lower concentrations of both leptin and MCP-1 were found in LBP patients compared to controls, whereas adiponectin did not differ among groups. MCP-1 was also lower in patients with non-persistent than in those with persistent LBP. Age, leptin (relative risk, 11.8; 95% CI, 3.9–35.8) and MCP-1 (relative risk, 2.7; 95% CI, 1.7–4.4) were independently associated with presence and duration of LBP. The combination of age, leptin and MCP-1 predicted 61% of the risk of LBP duration. The area under the curve of MCP-1 for distinguishing persistent from non-persistent LBP was 0.65 (95% CI, 0.54–0.76).

Conclusions:

Then results of our study suggest that leptin and MCP-1 may be promising biomarkers for diagnosis of acute LBP and its risk to become chronic.


Corresponding author: Prof. Giuseppe Lippi, Section of Clinical Biochemistry, University Hospital of Verona, Piazzale LA Scuro, 37134 Verona, Italy

  1. Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.

  2. Research funding: The study was supported by a grant (602736 PainOmics) of European Community (Call of Proposal FP7-HEALTH-2013-INNOVATION-1 – Topic: HEALTH.2013.2.2.1-5 – Understanding and controlling pain).

  3. Employment or leadership: None declared.

  4. Honorarium: None declared.

  5. Competing interests: The funding organization(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.

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Received: 2016-11-10
Accepted: 2016-12-3
Published Online: 2017-1-11
Published in Print: 2017-8-28

©2017 Walter de Gruyter GmbH, Berlin/Boston

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