“…Therefore, all the TRAP measured in this study was osteoclast-dependent. Although other biological markers of bone resorption are currently in fashion [3,22], TRAP meets more than enough criteria for considering it an adequate marker of bone resorption: 1) It correlates significantly and inversely with estrogen levels before and after Gn-RH agonist treatment [23], and in normal circumstances TRAP decreases with menarche and increases after menopause [24], 2) TRAP is elevated in diseases that are accompanied by a high remodeling rate [25], 3) TRAP correlates negatively with bone mass [23] and positively with alkaline phosphatase [26], as confirmed by this and other studies [23,26], 4) TRAP is sensitive to the effect of drugs that slow remodeling and reduce osteoclastic activity [27], 5) Osteoclastic TRAP is similar to serum TRAP 5b, as shown by electrophoretic mobility on acid gel [28], 6) Its specificity, because circulating TRAP 5b is exclusively osteoclastic in origin, increases its value as a marker of bone remodeling, 7) Finally, its determination in blood is easy [7] and free from the potential errors of markers quantitated in urine. Therefore, we do not think that more expensive markers, which require more complicated and sophisticated techniques, are necessary for evaluating bone resorption.…”