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抗骨质疏松药物对临床骨折风险降低的荟萃分析:直接和间接比较以及荟萃回归。

Meta-Analysis of Clinical Fracture Risk Reduction of Antiosteoporosis Drugs: Direct and Indirect Comparisons and Meta-Regressions.

机构信息

Department of Internal Medicine, Division of Endocrinology, Saint Louis University School of Medicine, St Louis, Missouri.

Department of Internal Medicine, Division of Endocrinology, Saint Louis University School of Medicine, St Louis, Missouri.

出版信息

Endocr Pract. 2021 Nov;27(11):1082-1092. doi: 10.1016/j.eprac.2021.06.015. Epub 2021 Jul 10.

Abstract

OBJECTIVE

Antiosteoporotic drug (AOD) trials have variabilities in duration and fracture risks. This study evaluated AOD's versus controls regarding reduction in relative rates and rate differences in vertebral and hip fractures and comparative costs.

METHODS

Primary randomized controlled trials of antiosteoporotic drugs in postmenopausal women with documentation of vertebral fracture rates or hip fracture rates were extracted from meta-analyses and PubMed through February 2021. Direct and indirect meta-analyses and meta-regressions analyzed the fracture reductions.

RESULTS

There were 24 randomized controlled trials of drug versus placebo (73 862 women) and 10 randomized controlled trials of drug versus drug. The reductions in the relative rates of vertebral fractures were significant for antiresorptive (alendronate, risedronate, zoledronate, denosumab, and raloxifene) and anabolic (teriparatide, abaloparatide, and romosozumab) drugs. Denosumab, teriparatide, and abaloparatide were more effective in reducing vertebral fracture rates than oral bisphosphates (all P < .05) but were not more effective in reducing vertebral fracture rates than zoledronate. The reductions in hip fracture rates were significant for alendronate, denosumab, and zoledronate (all P < .05), without significant differences among drugs. Anabolic drugs did not show significant hip fracture rate reduction. Meta-regression of rate differences enabled the calculation of costs per vertebral fracture prevented, which were estimated at >$100 000 for anabolic drugs and between $2289 and $28 947 for antiresorptive drugs. Many direct drug versus drug trials were underpowered to demonstrate benefits of one drug over another.

CONCLUSION

This study suggests goal-directed, cost-effective therapies relative to patient risk for vertebral and hip fractures. Anabolic drugs are better at preventing vertebral fractures than oral bisphosphonates. Anabolic drugs are not superior to zoledronate or denosumab and are substantially more expensive. When comparing drugs that prevented hip fractures, there was no statistical benefit of any drug.

摘要

目的

抗骨质疏松药物(AOD)试验在持续时间和骨折风险方面存在差异。本研究评估了 AOD 与对照组在降低椎体和髋部骨折的相对发生率和发生率差异以及比较成本方面的效果。

方法

从荟萃分析和 PubMed 中提取了绝经后妇女使用抗骨质疏松药物的随机对照试验,这些试验记录了椎体骨折发生率或髋部骨折发生率,这些试验通过元分析和直接和间接元分析和元回归分析来评估骨折减少的效果。

结果

共有 24 项药物与安慰剂(73862 名女性)的随机对照试验和 10 项药物与药物的随机对照试验。抗吸收剂(阿仑膦酸钠、利塞膦酸钠、唑来膦酸、地舒单抗和雷洛昔芬)和合成代谢药物(特立帕肽、abaloparatide 和 romosozumab)对椎体骨折发生率的降低有显著效果。地舒单抗、特立帕肽和 abaloparatide 比口服双膦酸盐更有效地降低椎体骨折发生率(均 P<0.05),但与唑来膦酸相比,降低椎体骨折发生率的效果并不显著。阿仑膦酸钠、地舒单抗和唑来膦酸对髋部骨折发生率的降低有显著效果(均 P<0.05),但药物之间无显著差异。合成代谢药物并未显示出髋部骨折发生率的显著降低。对率差的元回归使我们能够计算出每例椎体骨折预防的成本,估计合成代谢药物的成本超过 10 万美元,抗吸收药物的成本在 2289 美元至 28947 美元之间。许多直接的药物与药物试验在证明一种药物优于另一种药物的疗效方面的能力不足。

结论

本研究提示,针对椎体和髋部骨折的风险,采用目标导向、具有成本效益的治疗方法。合成代谢药物在预防椎体骨折方面优于口服双膦酸盐。合成代谢药物并不优于唑来膦酸或地舒单抗,而且成本要高得多。在比较预防髋部骨折的药物时,没有任何一种药物具有统计学上的优势。

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