beta(2)-microglobulin has been observed to behave as a biological mark
er of bone remodeling. We measured beta(2)-microglobulin and tartrate-
resistant acid phosphatase (TRAP), a specific biological marker of bon
e remodeling, in 225 women: healthy premenopausal controls, healthy po
stmenopausal controls, and patients with diseases characterized by enh
anced bone turnover (postmenopausal osteoporosis, primary hyperparathy
roidism, primary hyperthyroidism, polyostotic Paget's bone disease), a
nd in other Paget's group before and after calcitonin treatment. beta(
2)-microglobulin levels differed significantly between the healthy pre
menopausal women (n = 38) and the women with hyperparathyroidism (n =
20) compared with all the other groups. However, beta(2)-microglobulin
levels did not differ significantly between healthy postmenopausal wo
men (n = 38) and patients with Paget's bone disease (n = 40) (P = 0.50
95), or between women with postmenopausal osteoporosis (n = 30) and wo
men with hyperthyroidism (n = 20) (P = 0.7890). TRAP concentrations di
ffered significantly in all the groups paired except for women with Pa
get's bone disease and women with either hyperparathyroidism or hypert
hyroidism (P = 0.5179 and 0.6993, respectively); likewise, TRAP levels
did not differ significantly between the women with hyperparathyroidi
sm and those with hyperthyroidism (P = 0.7804). After calcitonin treat
ment, there was a 22% increase in beta(2)-microglobulin, a 17% decreas
e in TRAP, and a 39% decrease in alkaline phosphatase, all of which we
re significant at P < 0.0001. Our findings indicate that serum beta(2)
-microglobulin, like osteocalcin, behaves as a biological marker of re
modeling in a number of diseases with enhanced bone remodeling but not
in Paget's bone disease.