Serum levels of parathyroid hormone and markers of bone metabolism in patients with rheumatoid arthritis. Relationship to disease activity and glucocorticoid treatment

• Published in: Scandinavian journal of clinical and laboratory investigation 2001, Vol.61 (6), p.491-501
• Main Author: Jensen, M. Hansen, J. C. Madsen, G. Kollerup, M. Stoltenberg, A. Florescu, P. Schwarz, T.
• Format: Article
• Language: English
• Subjects: Anti-Inflammatory Agents - therapeutic use; Arthritis, Rheumatoid - blood; Arthritis, Rheumatoid - drug therapy; Biological and medical sciences; Biomarkers - blood; Bone and Bones - metabolism; Bone Metabolism Rheumatoid Arthritis; Cohort Studies; Cross-Sectional Studies; Diseases of the osteoarticular system; Glucocorticoids - therapeutic use; Humans; Inflammatory joint diseases; Medical sciences; Parathyroid Hormone - blood; Steroids
• ISSN: 0036-5513; 1502-7686
• DOI: 10.1080/00365510152567130

Objective : To evaluate the influence of inflammatory activity and glucocorticoid (GC) treatment on serum parathyroid hormone (s-PTH) and bone metabolism in patients with rheumatoid arthritis (RA). Furthermore, in patients with active RA, to examine the PTH secretion and Ca 2 + set point before and after treatment with GC. Methods : A range of biochemical markers of bone metabolism and calcium homeostasis were measured in 95 patients with definite RA stratified into groups according to disease activity and GC treatment. In a subgroup of 12 patients with active disease, initiating slow-acting-anti-rheumatic-drugs (SAARDs) &#45 GC, the PTH secretion and calcium set point were evaluated by use of the Cica clamp technique before and after 1 month of treatment. Results : S-osteocalcin, s-total alkaline phosphatase (s-TAP) and s-carboxyterminal crosslinked telopeptide of type I collagen (s-ICTP) were elevated in all groups. The levels of urine pyridinoline (Pyr) and s-albumin-corrected calcium (s-AlbCorrCa 2 + ) were elevated in patients with active disease and patients treated with GC. S-PTH and s-phosphate were within normal ranges. S-TAP, s-ICTP, Pyr and s-AlbCorrCa 2 + correlated positively with indices of disease activity. In the subgroups undergoing the Cica clamp technique, no difference in PTH responsiveness of B-Ca 2 + was unveiled. Conclusion : Neither active disease nor GC therapy appears to induce secondary hyperparathyroidism, nor is there an alteration in PTH responsiveness of B-Ca 2 + in patients with RA. The increased levels of markers of type I collagen metabolism (s-ICTP, Pyr) and s-AlbCorrCa 2 + in patients with active disease and patients treated with GC may be a result of increased degradation in synovium, cartilage and bone due to the inflammatory process.