URINARY COLLAGEN CROSS-LINK EXCRETION - A BETTER INDEX OF BONE-RESORPTION THAN HYDROXYPROLINE IN PAGETS-DISEASE OF BONE

Citation
Nat. Hamdy et al., URINARY COLLAGEN CROSS-LINK EXCRETION - A BETTER INDEX OF BONE-RESORPTION THAN HYDROXYPROLINE IN PAGETS-DISEASE OF BONE, Bone and mineral, 22(1), 1993, pp. 1-8
Citations number
26
Categorie Soggetti
Endocrynology & Metabolism
Journal title
ISSN journal
01696009
Volume
22
Issue
1
Year of publication
1993
Pages
1 - 8
Database
ISI
SICI code
0169-6009(1993)22:1<1:UCCE-A>2.0.ZU;2-J
Abstract
The 24 h urinary excretion of the collagen degradation products pyridi noline (Pyr) and deoxypyridinoline (Dpyr) have been proposed as specif ic and quantitative indices of bone resorption. We compared the value of the urinary excretion of Pyr and Dpyr to that of hydroxyproline (OH P) in 11 patients with Paget's disease of bone before and during treat ment with inhibitors of bone resorption, during admission to a metabol ic ward and maintenance on a gelatin-free diet. Pyr and Dpyr excretion rates were significantly correlated with those of OHP (r = 0.81 and 0 .77, respectively, P < 0.001; n = 106). The rate and degree of suppres sion of bone resorption were monitored in 6 of the patients similarly treated with intravenous dimethyl-APD at a dose of 4 mg/day for 10 day s, by daily measurements of the 24 h urinary excretion of Pyr, Dpyr an d OHP. Treatment with dimethyl-APD resulted in a decrease in the three indices of bone resorption. The percentage change from baseline value s was similar for the three indices, although changes in Dpyr appeared to follow more closely those of OHP. Our findings suggest that Pyr an d Dpyr are useful and specific indices of bone resorption in Paget's d isease of bone. They appear to confer no advantage, however, over the traditional determination of the urinary excretion of OHP, in the moni toring of response to treatment of such patients with inhibitors of bo ne resorption. Further studies are required to establish the value of these new biochemical indices of bone resorption, possibly in more sub tle disorders of bone metabolism such as osteoporosis.