We studied 77 women divided into postmenopausal osteoporotic and premenopau
sal and postmenopausal non-osteoporotic groups in order to evaluate bone me
tabolism and diagnostic value of biochemical markers of bone turnover in po
stmenopausal osteoporosis. Postmenopausal osteoporotic (n: 40), postmenopau
sal non-osteoporotic (n: 24) and premenopausal non-osteoporotic (n: 13) gro
ups were defined according to bone mineral density (BMD) scores obtained wi
th dual energy X-ray absorptiometry (DEXA). Urinary deoxypyridinoline (Dpd)
, pyridinoline (Pyd), serum total alkaline phosphatase (ALP), bone specific
alkaline phosphatase (BALP), osteocalcin (BGP), total calcium, phosphorus,
and creatinine levels were determined. Urinary Dpd and Pyd levels of postm
enopausal osteoporotic group (8.7 and 18.7 mu mol/mg creatinine) were signi
ficantly higher than postmenopausal control (5.1 and 11.7 mu mol/mg creatin
ine. p<0.0001) and premenopausal control (6.0 and 13.0 mu mol/mg creatinine
, p<0.0005 and p<0.001) groups. Bone formation markers were not significant
ly different between groups, although BGP correlated with Dpd and Pyd (r: 0
.26 and r: 0.31, p<0.05) in osteoporotic subjects. From receiver operating
curve (ROC) analysis Dpd had the best diagnostic value (0.846), followed by
Pyd (0.802) in evaluation of osteoporosis, whereas BALP (0.570) and BGP (0
.528) were relatively inefficient in the discrimination of postmenopausal o
steoporosis. This study suggests that bone resorption markers are more effi
cient than bone formation markers in the diagnosis of postmenopausal osteop
orosis. Urinary Dpd/creatinine ratio has the highest diagnostic value.