Abstract | BACKGROUND: METHODS: This randomised, double-blind, placebo-controlled study was conducted to determine the efficacy of 17.5 mg once-weekly risedronate in the prevention of hip fracture in women with PD. Patients were randomly assigned to 17.5 mg risedronate once a week (n=136) or a placebo (n=136) combined with daily 1000 IU of ergocalciferol. Incidence of hip fractures was compared between the two groups during the 2-year follow-up. RESULTS:
Hip fractures occurred in 15 patients in the placebo group and 3 patients in the risedronate group. The RR for hip fractures in the risedronate group as compared with the placebo group was 0.20 (95% CI 0.06 to 0.66). In the risedronate group, serum calcium levels decreased during the follow-up, while the levels in the placebo group increased. BMD increased by 3.4% in the risedronate group and decreased by 3.2% in the placebo group (p<0.01). CONCLUSIONS:
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Authors | Yoshihiro Sato, Jun Iwamoto, Yoshiaki Honda |
Journal | Journal of neurology, neurosurgery, and psychiatry
(J Neurol Neurosurg Psychiatry)
Vol. 82
Issue 12
Pg. 1390-3
(Dec 2011)
ISSN: 1468-330X [Electronic] England |
PMID | 21825080
(Publication Type: Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't, Retracted Publication)
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Chemical References |
- Bone Density Conservation Agents
- Ergocalciferols
- Risedronic Acid
- Etidronic Acid
- Calcium
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Topics |
- Aged
- Aged, 80 and over
- Bone Density
(drug effects)
- Bone Density Conservation Agents
(administration & dosage, therapeutic use)
- Calcium
(blood)
- Drug Administration Schedule
- Drug Therapy, Combination
(adverse effects, methods)
- Ergocalciferols
(administration & dosage, therapeutic use)
- Etidronic Acid
(administration & dosage, analogs & derivatives, therapeutic use)
- Female
- Hip Fractures
(blood, complications, drug therapy, prevention & control)
- Humans
- Parkinson Disease
(blood, complications, drug therapy)
- Risedronic Acid
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