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From the Department of Neurology (Dr. Sato), Mitate Hospital, Tagawa; Department of Sport Medicine (Dr. Iwamoto), Keio University School of Medicine, Tokyo; and Departments of Rehabilitation Medicine (Dr. Kanoko) and Vascular Biology (Dr. Satoh), Hirosaki University School of Medicine, Hirosaki, Japan.
Address correspondence and reprint requests to Dr. Yoshihiro Sato, Department of Neurology, Mitate Hospital, 3237 Yugeta, Tagawa 8260041, Japan; e-mail: y-sato{at}ktarn.or.jp
Background: There is a high incidence of hip fractures in patients with hemiplegic stroke. Bone mineral density (BMD) is decreased in the hemiplegic side in patients after stroke, correlating with the degree of paralysis and of hypovitaminosis D.
Objective: To evaluate the efficacy of risedronate in reducing the severity of osteoporosis and in decreasing the risk of hip fractures in elderly women following an acute stroke.
Methods: This was a 12-month, randomized, double blind, placebo-controlled trial. In a prospective study of stroke patients, 187 patients received a daily dose of 2.5 mg risedronate for 12 months, and the remaining 187 received placebo. Incidence of hip fracture was compared between the two groups at the endpoint of the study.
Results: Seven patients sustained hip fractures on the hemiplegic side in the placebo group, and one hip fracture occurred in the risedronate group (p = 0.0360; OR = 7.0). BMD increased by 1.5% and decreased by 4.9% in the risedronate group and placebo group (p < 0.0001). Urinary deoxypyridinoline, a bone resorption marker, decreased by 53.4% in the risedronate group and increased by 35.8% in the placebo group.
Conclusion: Treatment with risedronate increases bone mineral density in elderly women following an acute stroke and prevents hip fractures.
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Neurology 2005 64: 772-773.
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