Ks. Tsai et al., The effectiveness of cyclic and continuous oral clodronate therapy on bonedensity and markers in osteopenic postmenopausal women, CALCIF TIS, 64(5), 1999, pp. 384-388
Bisphosphonates have been used effectively to treat established osteoporosi
s and prevent postmenopausal bone loss. However, the optimal manner of its
administration-whether cyclic or continuous-has not been well established.
This study investigated the efficacy of cyclic and continuous oral administ
ration of clodronate in 54 newly identified osteopenic postmenopausal women
in a randomized, double-blind, crossover fashion. The participants were ra
ndomly separated into two groups. The cyclic group (n = 29) received 800 mg
twice daily of oral clodronate for 2 weeks every 3 months for the first 12
months followed by placebo for the second 12 months. The continuous group
(n = 25) received placebo in the first 12 months and ingested 400 mg of clo
dronate once daily for the second 12 months. The urinary amino-terminal (NT
X(TM)) and carboxy-terminal (CrossLaps(TM)) cross-linked fragments of type
I collagen, both markers of bone resorption, showed a marked decrease (25-5
0%) with both regimens during the period of active treatment. In the cyclic
group, the levels of these two markers increased in the second 12 months w
ith placebo, but did not return to the baseline completely. However, bone m
ineral density (BMD), determined by dual-energy X-ray absorptiometry (DXA),
showed no significant change of BMD at various sites after 1 year of activ
e treatment in both groups. Thoracic and lumbar spine X-ray showed no new v
ertebral fracture in either group after 2 years of treatment. With the two
treatment protocols in this study, oral clodronate was effective in decreas
ing postmenopausal bone resorption, causing no significant changes in BMD a
t various sites.