Osteoporosis International

, Volume 12, Issue 12, pp 1031–1035

Relationship Between Disease Activity and Serum Levels of Vitamin D Metabolites and Parathyroid Hormone in Ankylosing Spondylitis

  • U. Lange
  • O. Jung
  • J. Teichmann
  • G. Neeck
Original Article

DOI: 10.1007/s001980170013

Cite this article as:
Lange, U., Jung, O., Teichmann, J. et al. Osteoporos Int (2001) 12: 1031. doi:10.1007/s001980170013

Abstract:

Vertebral fractures due to osteoporosis are a common but frequently unrecognized complication of ankylosing spondylitis (AS) and various factors may contribute to the development of osteoporosis in AS. It is known that inflammatory activity in rheumatic disease (i.e., proinflammatory cytokines) itself plays a possible role in the pathophysiology of bone loss. 1,25-Dihydroxyvitamin D3 (1,25(OH)2D3) seems to be another possible candidate for mediatory function in regulating both the inflammatory process and bone turnover. The aim of this study was to evaluate the relation between disease activity, bone turnover and calciotropic hormones. In 70 patients with established AS and an age- and sex-matched control group, the relation between disease activity (erythrocyte sedimentation rate, C-reactive protein, Bath Ankylosing Spondylitis Disease Activity Index), and serum levels of vitamin D metabolites, parathyroid hormone (PTH), bone alkaline phosphatase (bAP) and urinary pyridinium crosslinks were determined. Serum levels of 1,25(OH)2D3 (p<0.01) and PTH (p<0.01) were negatively correlated with disease activity, the excretion of urinary pyridinium crosslinks showed a positive correlation with disease activity (p<0.01), and 1,25(OH)2D3 and PTH were positively correlated with bAP (p<0.01). These results indicate that high disease activity in AS is associated with an alteration in vitamin D metabolism and increased bone resorption. Furthermore, the decreased levels of 1,25(OH)2D3 may contribute to a negative calcium balance and inhibition of bone formation. Our results suggest further research is necessary to determine whether low levels of 1,25(OH)2D3 as an endogenous immune modulator suppressing activated T cells and cell proliferation may accelerate the inflammation process in AS.

Key words:Ankylosing spondylitis – Disease activity – Osteopenia – Osteoporosis – Vitamin D metabolism 

Copyright information

© International Osteoporosis Foundation and National Osteoporosis Foundation 2001

Authors and Affiliations

  • U. Lange
    • 1
  • O. Jung
    • 2
  • J. Teichmann
    • 3
  • G. Neeck
    • 1
  1. 1.Kerckhoff Clinic and Foundation, Department of Rheumatology, University of Giessen, Bad NauheimDE
  2. 2.IV. Medical Clinic – Nephrology, University of Frankfurt;DE
  3. 3. III. Medical Clinic, University of Giessen, GermanyDE

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