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Discovery of circulating blood biomarkers in patients with and without Modic changes of the lumbar spine: a preliminary analysis

  • Khaled Aboushaala,
  • Ana V. Chee,
  • Sheila J. Toro,
  • Rajko Vucicevic,
  • Catherine Yuh,
  • Jake Dourdourekas,
  • Ishani K. Patel,
  • Alejandro Espinoza-Orias,
  • Chundo Oh,
  • Lena Al-Harthi,
  • Jaro Karppinen,
  • Edward J. Goldberg,
  • Frank M. Phillips,
  • Matthew Colman,
  • Frances M. K. Williams,
  • Jeffrey A. Borgia,
  • Stefan Green,
  • Christopher Forsyth,
  • Howard S. An,
  • Dino Samartzis

摘要

Purpose

The following study aimed to determine the existence of blood biomarkers in symptomatic patients with or without lumbar Modic changes (MC).

Methods

A cross-sectional sub-analyses of a prospective cohort was performed. Fasting blood samples were collected from patients with and without lumbar MC who had undergone spinal fusion or microdiscectomy. An 80-plex panel and CCL5/RANTES were used to assess preoperative plasma cytokine concentrations. Patient demographics and imaging phenotypes were also assessed.

Results

Thirty-one subjects were analysed (n = 18 no MC; n = 13 MC). No significant differences were found in age, sex, body mass index, smoking and alcohol history, and surgical procedure (i.e. fusion, decompression) between the two groups (p > 0.05). Several statistically significant blood biomarkers in MC patients were identified, including elevated levels of C–C Motif Chemokine Ligand 5 (CCL5, p = 0.0006), while Macrophage Migration Inhibitory Factor (MIF) was significantly lower (p = 0.009). Additionally, C-X-C Motif Chemokine Ligand 5 (CXCL5, p = 0.052), Pentraxin 3 (PTX3, p = 0.06) and Galectin-3 (Gal-3, p = 0.07) showed potential relevance. Moreover, MC patients exhibited significantly higher levels of disc degeneration (p = 0.0001) and displacement severity (p = 0.020). Based on multivariate analyses and controlling for disc degeneration/displacement, CCL5 (OR 1.02; 95% CI 1.002–1.033; p = 0.028) and MIF (OR 0.60; 95% CI 0.382–0.951; p = 0.030) were independently associated with MC patients.

Conclusion

This “proof-of-concept” study is the first to identify specific and significantly circulating blood biomarkers associated with symptomatic patients with lumbar MC, independent of disc alterations of degeneration and/or bulges/herniations. Specifically, differences in CCL5 and MIF protein levels were significantly noted in MC patients compared to those without MC.