Serum levels of biomarkers of bone and cartilage destruction and new bone formation in different cohorts of patients with axial spondyloarthritis with and without tumor necrosis factor-alpha blocker treatment
2008

Biomarkers in Axial Spondyloarthritis and TNF-α Blocker Treatment

Sample size: 105 publication 10 minutes Evidence: moderate

Author Information

Author(s): Heiner Appel, Louise Janssen, Joachim Listing, René Heydrich, Martin Rudwaleit, Joachim Sieper

Primary Institution: Charité Berlin, Campus Benjamin Franklin

Hypothesis

The study investigates the relationship between inflammation, bone destruction, and new bone formation in patients with axial spondyloarthritis treated with TNF-α blockers.

Conclusion

The study found that successful treatment of inflammation in axial spondyloarthritis patients with TNF-α blockers is associated with new bone formation.

Supporting Evidence

  • Serum levels of MMP-3, VEGF, and BALP were stable in TNF-α blocker-naïve patients over 2 years.
  • Adalimumab treatment led to significant decreases in MMP-3 and VEGF levels.
  • BALP levels increased significantly after 36 to 52 weeks of adalimumab treatment.
  • A negative correlation was found between MMP-3 and BALP levels during treatment.
  • VEGF levels correlated with disease activity indicators like CRP and BASDAI.

Takeaway

Doctors looked at blood markers in patients with a type of arthritis to see how treatment helps their bones heal.

Methodology

The study measured serum levels of MMP-3, VEGF, and BALP in TNF-α blocker-naïve and adalimumab-treated patients over specified time periods.

Limitations

The study may have limitations related to sample size and the specific cohorts analyzed.

Participant Demographics

The TNF-α blocker-naïve cohort had a mean age of 37.75 years, with 61.97% male and 81.69% HLA-B27 positive; the adalimumab-treated cohort had a mean age of 40.12 years.

Statistical Information

P-Value

P < 0.001 for BALP increase in treated patients

Statistical Significance

p<0.001

Digital Object Identifier (DOI)

10.1186/ar2537

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