Department of Rheumatology , Research Center, Epidemiology and Biostatistics Sorbonne Paris Cité, Cochin Hospital, INSERM U1153, Paris Descartes University , Paris , France.
RMD Open. 2015 Apr 8;1(1):e000014. doi: 10.1136/rmdopen-2014-000014. eCollection 2015.
Corticosteroid-induced osteoporosis is the most common form of secondary osteoporosis and the first cause in young people. Bone loss and increased rate of fractures occur early after the initiation of corticosteroid therapy, and are then related to dosage and treatment duration. The increase in fracture risk is not fully assessed by bone mineral density measurements, as it is also related to alteration of bone quality and increased risk of falls. In patients with rheumatoid arthritis, a treat-to-target strategy focusing on low disease activity including through the use of low dose of prednisone, is a key determinant of bone loss prevention. Bone loss magnitude is variable and there is no clearly identified predictor of the individual risk of fracture. Prevention or treatment of osteoporosis should be considered in all patients who receive prednisone. Bisphosphonates and the anabolic agent parathyroid hormone (1-34) have shown their efficacy in the treatment of corticosteroid-induced osteoporosis. Recent international guidelines are available and should guide management of corticosteroid-induced osteoporosis, which remains under-diagnosed and under-treated. Duration of antiosteoporotic treatment should be discussed at the individual level, depending on the subject's characteristics and on the underlying inflammation evolution.
皮质类固醇性骨质疏松症是最常见的继发性骨质疏松症,也是年轻人骨质疏松症的首要病因。皮质类固醇治疗开始后早期即出现骨丢失和骨折发生率增加,与药物剂量和治疗持续时间相关。骨折风险的增加不能仅通过骨密度测量来充分评估,因为它还与骨质量的改变和跌倒风险增加有关。在类风湿关节炎患者中,通过使用小剂量泼尼松实现低疾病活动度的达标治疗策略是预防骨丢失的关键决定因素。骨丢失程度具有变异性,并且没有明确的个体骨折风险预测因素。应考虑对所有接受泼尼松治疗的患者预防或治疗骨质疏松症。双膦酸盐和合成代谢剂甲状旁腺激素(1-34)已显示出在治疗皮质类固醇性骨质疏松症方面的疗效。目前有国际指南可供使用,应指导皮质类固醇性骨质疏松症的管理,这种疾病仍存在诊断不足和治疗不足的情况。抗骨质疏松治疗的持续时间应根据个体的特点和潜在炎症的演变在个体层面进行讨论。