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Relationship between changes in bone mineral density and vertebral fracture risk associated with risedronate: greater increases in bone mineral density do not relate to greater decreases in fracture risk

Relationship between changes in bone mineral density and vertebral fracture risk associated with risedronate: greater increases in bone mineral density do not relate to greater decreases in fracture risk
Relationship between changes in bone mineral density and vertebral fracture risk associated with risedronate: greater increases in bone mineral density do not relate to greater decreases in fracture risk
Low bone mineral density (BMD) is correlated with increased fracture risk. Whether greater BMD increases induced by osteoporosis drugs are related to greater decreases in fracture risk is controversial. We analyzed the relationship between BMD change and fracture risk in postmenopausal osteoporotic women receiving antiresorptive treatment. The analysis combined data from three pivotal risedronate fracture end-point trials. Women received risedronate (n = 2047) or placebo (n = 1177) daily for up to 3 yr. The BMD and vertebral radiographs were assessed periodically during 3 yr. The estimated risk of new vertebral fracture was compared between patients whose BMD increased and those whose BMD decreased. Risedronate-treated patients whose BMD decreased were at a significantly greater risk (p = 0.003) of sustaining a vertebral fracture than patients whose BMD increased. The fracture risk was similar (about 10%) in risedronate-treated patients whose increases in BMD were < 5% (the median change from baseline) and in those whose increases were ? 5% (p = 0.453). The changes in lumbar spine BMD explained only 18% (95% confidence interval [CI], 10%, 26%; p < 0.001) of risedronate's vertebral fracture efficacy. Although patients showing an increase in BMD had a lower fracture risk than patients showing a decrease in BMD, greater increases in BMD did not necessarily predict greater decreases in fracture risk.
bone mineral density, vertebral fractures, risedronate, surrogate measure, osteoporosis, antiresorptive therapy
1094-6950
255-261
Watts, Nelson B.
5c0d14e9-020d-4e1f-802a-163636c5f0ea
Cooper, Cyrus
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Lindsay, Robert
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Eastell, Richard
b19615e4-bc97-4ddf-b8d7-7f48b7220228
Manhart, Michael D.
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Barton, Ian P.
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van Staa, Tjeerd-Pieter
f840d545-0e8d-40fe-9124-976826190cc3
Adachi, Jonathan D.
b332030f-9df9-4fb8-8547-7192a37b2522
Watts, Nelson B.
5c0d14e9-020d-4e1f-802a-163636c5f0ea
Cooper, Cyrus
e05f5612-b493-4273-9b71-9e0ce32bdad6
Lindsay, Robert
9508787f-a0b6-4155-95f7-33c57e4f56a0
Eastell, Richard
b19615e4-bc97-4ddf-b8d7-7f48b7220228
Manhart, Michael D.
790677b6-b0b1-4d29-8458-5e795a3e4db0
Barton, Ian P.
5e0ccee1-81ef-49d3-bd45-ec29e95f26f7
van Staa, Tjeerd-Pieter
f840d545-0e8d-40fe-9124-976826190cc3
Adachi, Jonathan D.
b332030f-9df9-4fb8-8547-7192a37b2522

Watts, Nelson B., Cooper, Cyrus, Lindsay, Robert, Eastell, Richard, Manhart, Michael D., Barton, Ian P., van Staa, Tjeerd-Pieter and Adachi, Jonathan D. (2004) Relationship between changes in bone mineral density and vertebral fracture risk associated with risedronate: greater increases in bone mineral density do not relate to greater decreases in fracture risk. Journal of Clinical Densitometry, 7 (3), 255-261.

Record type: Article

Abstract

Low bone mineral density (BMD) is correlated with increased fracture risk. Whether greater BMD increases induced by osteoporosis drugs are related to greater decreases in fracture risk is controversial. We analyzed the relationship between BMD change and fracture risk in postmenopausal osteoporotic women receiving antiresorptive treatment. The analysis combined data from three pivotal risedronate fracture end-point trials. Women received risedronate (n = 2047) or placebo (n = 1177) daily for up to 3 yr. The BMD and vertebral radiographs were assessed periodically during 3 yr. The estimated risk of new vertebral fracture was compared between patients whose BMD increased and those whose BMD decreased. Risedronate-treated patients whose BMD decreased were at a significantly greater risk (p = 0.003) of sustaining a vertebral fracture than patients whose BMD increased. The fracture risk was similar (about 10%) in risedronate-treated patients whose increases in BMD were < 5% (the median change from baseline) and in those whose increases were ? 5% (p = 0.453). The changes in lumbar spine BMD explained only 18% (95% confidence interval [CI], 10%, 26%; p < 0.001) of risedronate's vertebral fracture efficacy. Although patients showing an increase in BMD had a lower fracture risk than patients showing a decrease in BMD, greater increases in BMD did not necessarily predict greater decreases in fracture risk.

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More information

Published date: 2004
Keywords: bone mineral density, vertebral fractures, risedronate, surrogate measure, osteoporosis, antiresorptive therapy

Identifiers

Local EPrints ID: 26116
URI: http://eprints.soton.ac.uk/id/eprint/26116
ISSN: 1094-6950
PURE UUID: d7768828-28af-4992-8564-c22583798e6c
ORCID for Cyrus Cooper: ORCID iD orcid.org/0000-0003-3510-0709

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Date deposited: 12 Apr 2006
Last modified: 18 Mar 2024 02:44

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Contributors

Author: Nelson B. Watts
Author: Cyrus Cooper ORCID iD
Author: Robert Lindsay
Author: Richard Eastell
Author: Michael D. Manhart
Author: Ian P. Barton
Author: Tjeerd-Pieter van Staa
Author: Jonathan D. Adachi

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