Urinary assays for type I collagen metabolites provide a non invasive index
of bone resorption in humans, and are widely used in the management of pat
ients with metabolic bone diseases. The specific aims of this study were to
investigate the feasibility of using commercial human assay kits for quant
ifying the urinary excretion of type I collagen metabolites in dogs of diff
erent ages. Urine and serum samples were collected from 35 beagle dogs in f
ive age groups (0 to 1 years, 1 to 2 years; 2 to 3 years; 3 to 7 years; > 8
years old). Urinary concentrations of pyridinoline (Pyd), deoxypyridinolin
e (Dpd), and the carboxy- and amino-terminal crosslinked telopeptides of ty
pe I collagen (CTx and NTx, respectively) were measured with commercial enz
yme-linked immunoassay kits. Serum concentrations of another type I collage
n metabolite, the carboxy-terminal cross-linked teloptide of type I collage
n (ICTP), were measured with a commercial radioimmunoassay.
Dilutional studies indicated that the four urinary assays show specific cro
ss-reactivity with canine urine. Age-related differences in urinary marker
excretion were identified, with young dogs excreting the highest concentrat
ions of Pyd, Dpd, NTx and CTx. The correlation between the individual urina
ry markers was excellent (r = 0.87 to 0.98), while the correlation between
serum ICTP and individual urinary markers was weaker (r = 0.52 to 0.64). Th
ese results validate the usefulness of the commercial assay kits in monitor
ing type I collagen metabolism in dogs. Histomorphometric studies have conf
irmed the relationship between collagen degradation and bone resorption in
humans, and similar studies are now needed in dogs. (C) 2000 Harcourt Publi
shers Ltd.