Associations of vascular and bone status in arthritis patients

Anita Pusztai1, Attila Hamar1, Monika Czókolyová1

  • 1Division of Rheumatology, Faculty of Medicine, University of Debrecen, Nagyerdei Str 98, Debrecen, 4032, Hungary.

Scientific Reports
|October 1, 2021
PubMed

Insights

Rheumatoid arthritis and ankylosing spondylitis patients treated with anti-TNF therapy show links between bone metabolism and vascular disease. Inflammation and disease activity in arthritis may influence both bone and vascular health.

Area of Science:

  • Rheumatology
  • Vascular Biology
  • Bone Metabolism

Background:

  • Rheumatoid arthritis (RA) and ankylosing spondylitis (AS) are associated with increased risk of cardiovascular (CV) disease and osteoporosis (OP).
  • Understanding the interplay between bone metabolism and vascular pathophysiology in these conditions is crucial for patient management.

Purpose of the Study:

  • To assess bone and vascular biomarkers and parameters in RA and AS patients.
  • To determine the effect of 1-year anti-TNF therapy on these markers.
  • To identify correlations between vascular pathophysiology and bone metabolism.

Main Methods:

  • A 12-month follow-up study included 36 RA patients and 17 AS patients treated with anti-TNF agents (etanercept, certolizumab pegol, or infliximab).
  • Bone and vascular markers were measured using ELISA.
  • Bone density was assessed by DXA and quantitative CT (QCT).
  • Vascular parameters included flow-mediated dilation (FMD), intima-media thickness (IMT), and pulse-wave velocity (PWV) measured by ultrasound.

Main Results:

  • Multiple correlation analyses revealed significant associations between bone and vascular markers.
  • Osteoprotegerin, sclerostin, and cathepsin K correlated with FMD, IMT, and PWV, respectively.
  • Bone mineral density (BMD) measured by QCT inversely correlated with IMT, while platelet-derived growth factor BB and IMT correlated with BMD.
  • Anti-TNF treatment, along with baseline osteocalcin, P1NP, or vitamin D3 levels, influenced one-year changes in IMT.
  • Disease activity indices and CRP levels affected correlations between bone and vascular markers.

Conclusions:

  • Significant correlations exist between bone and vascular biomarkers in RA and AS patients undergoing anti-TNF therapy.
  • Specific bone markers are associated with vascular pathophysiology, and vice versa.
  • Systemic inflammation and disease activity in arthritis appear to be key drivers of both vascular and bone disease.

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