San Francisco Coordinating Center, California Pacific Medical Research Institute, San Francisco, CA, USA.
J Bone Miner Res. 2012 Aug;27(8):1804-10. doi: 10.1002/jbmr.1625.
The WHO Fracture Risk Assessment Tool (FRAX; http://www.shef.ac.uk/FRAX) estimates the 10-year probability of major osteoporotic fracture. Clodronate and bazedoxifene reduced nonvertebral and clinical fracture more effectively on a relative scale in women with higher FRAX scores. We used data from the Fracture Intervention Trial (FIT) to evaluate the interaction between FRAX score and treatment with alendronate. We combined the Clinical Fracture (CF) arm and Vertebral Fracture (VF) arm of FIT. The CF and VF arm of FIT randomized 4432 and 2027 women, respectively, to placebo or alendronate for 4 and 3 years, respectively. FRAX risk factors were assessed at baseline. FRAX scores were calculated by WHO. We used Poisson regression models to assess the interaction between alendronate and FRAX score on the risk of nonvertebral, clinical, major osteoporotic, and radiographic vertebral fractures. Overall, alendronate significantly reduced the risk of nonvertebral fracture (incidence rate ratio [IRR] 0.86; 95% confidence interval [CI], 0.75-0.99), but the effect was greater for femoral neck (FN) bone mineral density (BMD) T-score ≤ -2.5 (IRR 0.76; 95% CI, 0.62-0.93) than for FN T-score > -2.5 (IRR 0.96; 95% CI, 0.80-1.16) (p = 0.02, interaction between alendronate and FN BMD). However, there was no evidence of an interaction between alendronate and FRAX score with FN BMD for risk of nonvertebral fracture (interaction p = 0.61). The absolute benefit of alendronate was greatest among women with highest FRAX scores. Results were similar for clinical fractures, major osteoporotic fractures, and radiographic vertebral fractures and whether or not FRAX scores included FN BMD. Among this cohort of women with low bone mass there was no significant interaction between FRAX score and alendronate for nonvertebral, clinical or major osteoporotic fractures, or radiographic vertebral fractures. These results suggest that the effect of alendronate on a relative scale does not vary by FRAX score. A randomized controlled trial testing the effect of antifracture agents among women with high FRAX score but without osteoporosis is warranted.
世界卫生组织(WHO)骨折风险评估工具(FRAX;http://www.shef.ac.uk/FRAX)估计了 10 年内主要骨质疏松性骨折的概率。氯屈膦酸盐和巴多昔芬在 FRAX 评分较高的女性中,在相对比例上更有效地减少了非椎体和临床骨折。我们使用骨折干预试验(FIT)的数据来评估 FRAX 评分与阿伦膦酸钠治疗之间的相互作用。我们将 FIT 的临床骨折(CF)组和椎体骨折(VF)组合并。FIT 的 CF 和 VF 组分别将 4432 名和 2027 名女性随机分配至安慰剂或阿伦膦酸钠组,分别接受 4 年和 3 年的治疗。FRAX 危险因素在基线时进行评估。FRAX 评分由世界卫生组织计算。我们使用泊松回归模型评估阿伦膦酸钠与 FRAX 评分对非椎体、临床、主要骨质疏松性和影像学椎体骨折风险的相互作用。总体而言,阿伦膦酸钠显著降低了非椎体骨折的风险(发病率比 [IRR] 0.86;95%置信区间 [CI],0.75-0.99),但对于股骨颈(FN)骨密度(BMD)T 评分≤-2.5(IRR 0.76;95%CI,0.62-0.93)的效果大于 FN T 评分>-2.5(IRR 0.96;95%CI,0.80-1.16)(p=0.02,阿伦膦酸钠与 FN BMD 之间的相互作用)。然而,对于非椎体骨折的风险,没有证据表明阿伦膦酸钠与 FRAX 评分与 FN BMD 之间存在相互作用(相互作用 p=0.61)。在 FRAX 评分最高的女性中,阿伦膦酸钠的绝对获益最大。对于临床骨折、主要骨质疏松性骨折和影像学椎体骨折,以及 FRAX 评分是否包含 FN BMD,结果均相似。在这群低骨量的女性中,FRAX 评分与阿伦膦酸钠之间对于非椎体、临床或主要骨质疏松性骨折或影像学椎体骨折没有显著的相互作用。这些结果表明,阿伦膦酸钠的相对疗效在 FRAX 评分上没有差异。需要进行一项随机对照试验来测试抗骨折药物在 FRAX 评分高但无骨质疏松症的女性中的疗效。