Abstract | BACKGROUND: The aim of this study was to assess the efficacy, tolerability and safety of risedronate in adults with CF. METHODS: Patients with a lumbar spine (LS), total hip (TH) or femoral neck (FN) bone mineral density (BMD) Z-score of -1 or less were randomised to receive risedronate 35 mg weekly or placebo, and calcium (1g)+ vitamin D(3) (800IU). RESULTS: At baseline, BMD Z-scores in the risedronate (n=17) and placebo (n=19) groups were similar. By 24 months, 7/17 risedronate patients vs 0/19 placebo patients stopped the study medication due to bone pain. After 24 months treatment, the mean difference (95% CI) in change in LS, TH and FN BMD between the risedronate vs placebo groups was 4.3% (0.4, 8.2) p=0.03; 4.0% (-0.5, 8.6) p=0.08; and 2.4% (-3.5, 8.2) p=0.41. CONCLUSIONS: After two years treatment there was a significant increase in LS BMD with weekly risedronate compared to placebo.
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Authors | Charles S Haworth, Linda Sharples, Vikki Hughes, Sarah L Elkin, Margaret E Hodson, Steven P Conway, Christine Etherington, J Stuart Elborn, Jackie Rendall, Ella Wheaton, Emma Kadri, Jane Elliott, Helen C Barker, Philip W P Bearcroft, Thinn Hlaing, Juliet E Compston |
Journal | Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society
(J Cyst Fibros)
Vol. 10
Issue 6
Pg. 470-6
(Dec 2011)
ISSN: 1873-5010 [Electronic] Netherlands |
PMID | 21849264
(Publication Type: Journal Article, Multicenter Study, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2011 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved. |
Chemical References |
- Bone Density Conservation Agents
- Risedronic Acid
- Etidronic Acid
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Topics |
- Adult
- Bone Density
(drug effects)
- Bone Density Conservation Agents
(administration & dosage, pharmacology)
- Cystic Fibrosis
- Drug Administration Schedule
- Etidronic Acid
(administration & dosage, analogs & derivatives, pharmacology)
- Female
- Humans
- Male
- Risedronic Acid
- Single-Blind Method
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