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糖皮质激素性骨质疏松症:发病机制、诊断与管理

Glucocorticoid-induced osteoporosis: pathogenesis, diagnosis, and management.

作者信息

McIlwain Harris H

机构信息

Tampa Medical Group Research, 4700 N. Habana Avenue, Suite 303, Tampa, FL 33614, USA.

出版信息

Prev Med. 2003 Feb;36(2):243-9. doi: 10.1016/s0091-7435(02)00019-1.

Abstract

Glucocorticoid-induced bone loss is dose- and duration-related, develops rapidly (within months of therapy), and leads to an increased risk of fractures. Moreover, less than one in four patients prescribed oral glucocorticoids receive any treatment to prevent or treat osteoporosis. The American College of Rheumatology recommends bisphosphonate therapy to prevent bone loss in most patients beginning long-term glucocorticoid therapy (prednisone equivalent of > or =5 mg/day for at least 3 months), and in men and postmenopausal women receiving long-term glucocorticoids who have an abnormal bone mineral density (T score below -1). Patients with glucocorticoid-induced osteoporosis are at particularly high risk for fractures, and should be treated aggressively to reduce fracture risk. Risedronate is approved in the United States for both prevention and treatment of glucocorticoid-induced osteoporosis and alendronate is approved for treatment. Both drugs increase bone mass in patients with established glucocorticoid-induced osteoporosis. Risedronate has been shown to significantly reduce the incidence of fractures after 1 year of treatment. Prevention or treatment of glucocorticoid-induced bone loss is recommended for patients at risk.

摘要

糖皮质激素诱导的骨质流失与剂量和疗程相关,发展迅速(在治疗数月内),并导致骨折风险增加。此外,在接受口服糖皮质激素治疗的患者中,不到四分之一的人接受任何预防或治疗骨质疏松症的措施。美国风湿病学会建议,对于大多数开始长期糖皮质激素治疗(泼尼松等效剂量≥5毫克/天,至少3个月)的患者,以及骨矿物质密度异常(T值低于-1)的接受长期糖皮质激素治疗的男性和绝经后女性,采用双膦酸盐治疗以预防骨质流失。糖皮质激素诱导的骨质疏松症患者骨折风险特别高,应积极治疗以降低骨折风险。利塞膦酸钠在美国被批准用于预防和治疗糖皮质激素诱导的骨质疏松症,阿仑膦酸钠被批准用于治疗。两种药物均可增加已确诊的糖皮质激素诱导的骨质疏松症患者的骨量。利塞膦酸钠已被证明在治疗1年后可显著降低骨折发生率。建议对有风险的患者预防或治疗糖皮质激素诱导的骨质流失。

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