Leslie Dan Faculty of Pharmacy, University of Toronto, Toronto, Canada.
Institute for Clinical Evaluative Sciences, Toronto, Canada.
J Bone Miner Res. 2018 Mar;33(3):419-429. doi: 10.1002/jbmr.3318. Epub 2017 Dec 11.
The benefit of oral bisphosphonates in reducing fracture risk in glucocorticoid-induced osteoporosis is controversial. We aimed to estimate the effectiveness of oral bisphosphonates in reducing fracture risk in a cohort of new chronic oral glucocorticoid users. We created three matched cohorts using health care administrative data from Ontario, Canada. We included residents aged 66 years and older initiating chronic oral glucocorticoids (≥450 mg prednisone equivalent and ≥2 glucocorticoid prescriptions within a 6-month window) between January 1998 and September 2014. Exposed patients were those who initiated an oral bisphosphonate (alendronate, etidronate, or risedronate) within the first 6 months of starting chronic oral glucocorticoid therapy. Exposed cohorts (3945 alendronate, 5825 risedronate, and 8464 etidronate) were each matched 1:1 to unexposed patients on glucocorticoid exposure, fracture risk factors, and propensity score. We examined incident hip (primary outcome), vertebral, forearm, and humerus fractures using Cox proportional hazard models. Alendronate (hazard ratio [HR] = 0.46, 95% confidence interval [CI] 0.25-0.80) and risedronate (HR = 0.58, 95% CI 0.36-0.90) were associated with reduced hip fracture risk. Alendronate (HR = 0.52, 95% CI 0.39-0.68), etidronate (HR = 0.59, 95% CI 0.48-0.73) and risedronate (HR = 0.47 95% CI 0.36-0.60) were associated with reduced vertebral fracture risk. No risk reduction in forearm or humerus fractures was apparent for any bisphosphonate. Among older chronic glucocorticoid initiators, all oral bisphosphonates reduced vertebral fracture risk, yet only alendronate and risedronate reduced hip fracture risk. Results were similar between men and women. We provided compelling evidence that early initiation of oral bisphosphonates during chronic oral glucocorticoid therapy is beneficial to prevent osteoporotic fractures. © 2017 American Society for Bone and Mineral Research.
口服双膦酸盐在减少糖皮质激素诱导性骨质疏松症骨折风险方面的益处存在争议。我们旨在评估在新的慢性口服糖皮质激素使用者队列中,口服双膦酸盐降低骨折风险的效果。我们使用来自加拿大安大略省的医疗保健管理数据创建了三个匹配队列。我们纳入了 1998 年 1 月至 2014 年 9 月期间开始接受慢性口服糖皮质激素治疗(≥450mg 泼尼松等效物且在 6 个月内开具≥2 张糖皮质激素处方)且年龄≥66 岁的居民。暴露组患者在开始慢性口服糖皮质激素治疗的前 6 个月内开始使用口服双膦酸盐(阿仑膦酸钠、依替膦酸钠或利塞膦酸钠)。暴露队列(3945 例阿仑膦酸钠、5825 例利塞膦酸钠和 8464 例依替膦酸钠)均按糖皮质激素暴露、骨折风险因素和倾向评分 1:1 与未暴露患者匹配。我们使用 Cox 比例风险模型检查了髋部(主要结局)、椎体、前臂和肱骨骨折的发生率。阿仑膦酸钠(风险比[HR] = 0.46,95%置信区间[CI] 0.25-0.80)和利塞膦酸钠(HR = 0.58,95%CI 0.36-0.90)与髋部骨折风险降低相关。阿仑膦酸钠(HR = 0.52,95%CI 0.39-0.68)、依替膦酸钠(HR = 0.59,95%CI 0.48-0.73)和利塞膦酸钠(HR = 0.47,95%CI 0.36-0.60)与椎体骨折风险降低相关。任何双膦酸盐均未显示前臂或肱骨骨折风险降低。在老年慢性糖皮质激素初治者中,所有口服双膦酸盐均降低了椎体骨折风险,但只有阿仑膦酸钠和利塞膦酸钠降低了髋部骨折风险。男性和女性的结果相似。我们提供了令人信服的证据表明,在慢性口服糖皮质激素治疗期间早期开始口服双膦酸盐有益于预防骨质疏松性骨折。