The effect on bone mass and bone markers of different doses of ibandronate: A new bisphosphonate for prevention and treatment of postmenopausal osteoporosis: A 1-year, randomized, double-blind, placebo-controlled dose-finding study

被引:124
作者
Ravn, P [1 ]
Clemmesen, B [1 ]
Riis, BJ [1 ]
Christiansen, C [1 ]
机构
[1] CTR CLIN & BASIC RES,DK-2750 BALLERUP,DENMARK
关键词
osteoporosis; bone turnover; bisphosphonates; ibandronate;
D O I
10.1016/S8756-3282(96)00229-3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The present article describes the results from a phase II dose finding study of the effect of ibandronate, a new, third generation bisphosphonate, in postmenopausal osteoporosis, One hundred and eighty postmenopausal, white women, at least 10 years past a natural menopause, with osteopenia defined as a bone mineral density (BMD) in the distal forearm at least 1.5 SD below the premenopausal mean, entered and 141 (78%) completed a 12 months randomized, double-blind, placebo-controlled study, The women received 0.25, 0.5, 1.0, 2.5, or 5.0 mg ibandronate daily or placebo, All women received a daily calcium supplementation of 1000 mg Ca2+, Bone mass and biochemical markers of bone turnover were measured every 3 months throughout the study period, The average changes in bone mass showed positive outcome in all regions in the groups receiving ibandronate 2.5 and 5.0 mg, The responses in the two groups were not significantly different, although there was a tendency toward a higher response in bone mass in the group receiving ibandronate 2.5 mg, where the increase in BMD was 4.6 +/- 3.1% (SD) in the spine (p < 0.001), 1.3 +/- 3.0% (SD) to 3.5 +/- 5.3% (SD) in the different regions of the proximal femur ip < 0.03 to p < 0.002), and 2.0 +/- 1.9% (SD) in total body bone mineral content (BMC) (p < 0.001), There was no significant changes in bone mass in the group receiving calcium (placebo) and ibandronate 0.25 mg, Dose-related responses were found in all biochemical markers of bone turnover, In average, serum osteocalcin decreased 13 +/- 14% (SD) (placebo) and 35 +/- 14%(SD) (5.0 mg), Urinary excretions of breakdown products of type I collagen decreased 35 +/- 21% (SD) (placebo) and 78 +/- 28 % (SD) (5.0 mg), p < 0.001 in all groups, In conclusion, the results suggest that ibandronate treatment increases bone mass in all skeletal regions in a dose dependent manner with 2.5 mg being the most effective dose, Ibandronate treatment reduces bone turnover to premenopausal levels and is well tolerated. (C) 1996 by Elsevier Science Inc.
引用
收藏
页码:527 / 533
页数:7
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