We demonstrated the characteristics of bone metabolism in osteoporotic women who responded to activate-depress-free-repeat (ADFR) treatment for 6 months.
Forty female outpatients with postmenopausal or senile osteoporosis, aged 48 to 89 years (mean 72.6±1.8 years), were divided into an ADFR treatment group and a control group. ADFR treatment was as follows: activate stage, alfacalcidol (Alfarol
®) 1.0μg/day for 2 weeks; depress stage, elcatonin (Elcitonin
®) 10 units×6/2 weeks for 2 weeks; free stage, Alfarol 0.5μg/day for 4 weeks. The control group was treated with calcium lactate 5.0g/day. Bone mineral density (BMD) was measured by the digital image processing (DIP) method.
After 6 months of treatment, percent changes in BMD (BMD%) and alkaline phosphatase (Alp%) in the ADFR group were significantly higher than those in the control group (p<0.05 and p<0.01, respectively). The ADFR group was subdivided into a responder group (n=14) whose BMD% increased, and a non-responder group (n=6) whose BMD% decreased. Alp% in the responder group was significantly greater (p<0.05), whereas the percent changes in both urinary calcium/creatinine% (U-Ca/Cr%) and urinary hydroxyproline/creatinine% (U-HP/Cr%) were significantly lower than those in the non-responder group (p<0.05 and p<0.01, respectively).
These results showed that the bone metabolism characteristics of responders to ADFR treatment for 6 months were higher Alp% and lower U-Ca/Cr% and U-HP/Cr% as compared with those of non-responders.
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