Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
Dr. David Hanley Osteoporosis Centre, Richmond Road Diagnostic & Treatment Centre, 1820 Richmond Road SW, Calgary, Alberta, T2T 5C7, Canada.
Osteoporos Int. 2021 Jul;32(7):1313-1320. doi: 10.1007/s00198-021-05826-5. Epub 2021 Jan 12.
Prevention of early menopausal bone loss may reduce the future burden of osteoporosis. In this modelling exercise, an osteoporosis prevention strategy involving 5-year infusions of zoledronic acid, beginning early in menopause, reduced long-term fracture risk and the proportion of aging women with femoral neck densitometric osteoporosis. This strategy warrants further evaluation.
Preventing early menopausal bone loss may substantially reduce the future burden of osteoporosis. We modelled the effects of infrequent zoledronic acid infusions on long-term fracture risk.
Data from the Canadian Multicentre Osteoporosis Study (CaMos) were used to determine the expected natural history of femoral neck areal bone mineral density (BMD) and fracture risk (using FRAX®) from ages 50-80 for women with no antiresorptive drug exposures. We modelled the effects of three infusions of zoledronic acid (at ages 50, 55, 60) on long-term fracture risk, assuming this intervention would preserve BMD until age 65 years, followed by losses mirroring early menopausal BMD loss.
At age 65, untreated women and zoledronic acid recipients had expected mean (SD) femoral neck T-scores of - 1.5(1.0) and - 0.8(1.0), 10-year major osteoporotic fracture (MOF) risks of 9.8%(5.0) and 8.0%(3.7) and hip fracture risks of 1.7%(2.4) and 0.8%(1.2), respectively. At age 80, untreated women and zoledronic acid recipients had expected femoral neck T-scores of - 1.9(0.9) and - 1.4(0.9), MOF risks of 17.9%(8.2) and 14.9%(6.4) and hip fracture risks of 6.3%(6.2) and 4.4%(4.5), respectively. The expected proportion of women with femoral neck T-score ≤ - 2.5 was 14.9% for untreated women and 3.8% for zoledronic acid recipients at age 65, increasing to 28.1% and 12.0%, respectively, at age 80. Numbers-needed-to-treat to prevent one case of densitometric osteoporosis were 9 at age 65 and 5 at age 80.
Infrequent infusions of zoledronic acid, initiated early in menopause, are expected to reduce long-term fracture risk and result in a substantial reduction in the proportion of women with densitometric osteoporosis after age 65.
预防绝经早期的骨质流失可能会降低未来骨质疏松症的负担。本研究通过建立模型,评估在绝经早期开始、每 5 年静脉输注唑来膦酸 5 年的骨质疏松预防策略对长期骨折风险和股骨颈骨密度骨质疏松症的老年女性比例的影响。
使用加拿大骨质疏松多中心研究(CaMos)的数据,确定无抗吸收药物暴露的女性从 50 岁到 80 岁的股骨颈面积骨矿物质密度(BMD)和骨折风险(使用 FRAX®)的自然史。我们建立了模型,评估了三剂唑来膦酸(50 岁、55 岁、60 岁)对长期骨折风险的影响,假设该干预措施可以将 BMD 保持到 65 岁,之后的 BMD 损失与绝经早期的 BMD 损失相似。
在 65 岁时,未治疗的女性和唑来膦酸组的预期平均(SD)股骨颈 T 评分分别为-1.5(1.0)和-0.8(1.0),10 年主要骨质疏松性骨折(MOF)风险分别为 9.8%(5.0)和 8.0%(3.7),髋部骨折风险分别为 1.7%(2.4)和 0.8%(1.2)。在 80 岁时,未治疗的女性和唑来膦酸组的预期股骨颈 T 评分分别为-1.9(0.9)和-1.4(0.9),MOF 风险分别为 17.9%(8.2)和 14.9%(6.4),髋部骨折风险分别为 6.3%(6.2)和 4.4%(4.5)。未治疗的女性在 65 岁时,预计有 14.9%的女性股骨颈 T 评分≤-2.5,而唑来膦酸组的这一比例为 3.8%,到 80 岁时,这一比例分别上升至 28.1%和 12.0%。预防一例骨密度骨质疏松症的需要治疗人数(NNT)在 65 岁时为 9 人,在 80 岁时为 5 人。
在绝经早期开始、每 5 年静脉输注唑来膦酸的方案预计会降低长期骨折风险,并在 65 岁以后显著降低股骨颈骨密度骨质疏松症的女性比例。