Tamura Yasuhiro, Okinaga Hiroko, Takami Hiroshi
Department of Internal Medicine, Teikyo University School of Medicine, 2-11-1 Kaga, Itabashi-Ku, Tokyo 173-8605, Japan.
Biomed Pharmacother. 2004 Nov;58(9):500-4. doi: 10.1016/j.biopha.2004.08.018.
Glucocorticoids are important drugs in the treatment of variety diseases, but long-term period use can lead to various adverse effects, including osteoporosis. Glucocorticoid-induced osteoporosis is mainly caused by inhibition of osteoblastic bone formation, which results not only in decreased bone mineral density, but reduction of bone strength by trabecular thinning in bone microstructures. The evidence suggests that daily oral glucocorticoid doses higher than 5 mg prednisolone or equivalent increase the risk of fracture within 3-6 months after the start of therapy. High-dose inhaled glucocorticoids may also increase fracture risk. The diagnostic procedures are similar to those for primary osteoporosis, but the diagnostic threshold for bone mineral density needs to be higher than that for primary osteoporosis. Treatment with vitamin D, calcitonin, sex hormone replacement, and bisphosphonates has been shown to be effective, and bisphosphonates have been demonstrated to be the most valuable drugs for glucocorticoid-induced osteoporosis. There are several lines of evidence indicating that they are effective in preventing and treating low bone mineral density and in reducing fracture risk.
糖皮质激素是治疗多种疾病的重要药物,但长期使用会导致各种不良反应,包括骨质疏松。糖皮质激素诱导的骨质疏松主要是由成骨细胞骨形成受抑制引起的,这不仅会导致骨矿物质密度降低,还会因骨微结构中的小梁变薄而使骨强度降低。有证据表明,每日口服泼尼松龙剂量高于5毫克或等效剂量,在治疗开始后的3至6个月内会增加骨折风险。高剂量吸入糖皮质激素也可能增加骨折风险。诊断程序与原发性骨质疏松症相似,但骨矿物质密度的诊断阈值需要高于原发性骨质疏松症。维生素D、降钙素、性激素替代疗法和双膦酸盐治疗已被证明是有效的,双膦酸盐已被证明是治疗糖皮质激素诱导的骨质疏松最有价值的药物。有几条证据表明,它们在预防和治疗低骨矿物质密度以及降低骨折风险方面是有效的。