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根据骨折风险状况确定骨质疏松症的双膦酸盐药物假期

Bisphosphonate drug holidays in osteoporosis according to fracture risk profile.

作者信息

Salmoral Asunción, Peris P, López Medina C, Flórez H, Barceló M, Pascual Pastor M, Ros I, Grados D, Aguado P, García S, López L, Gifre L, Cerdá D, Aguilar F J, Panero B, Costa E, Casado E, Hernández B, Martínez Ferrer A, Graña J, Gómez I, Guañabens N

机构信息

Department of Rheumatology, University Hospital Reina Sofía, Maimonides Institute for Biomedical Research of Córdoba (IMIBIC), University of Córdoba, Cordoba, Spain.

Department of Rheumatology, Hospital Clínic, Institut d'Investigacions Biomediques August Pi I Sunyer (IDIBAPS), University of Barcelona, Barcelona, Spain.

出版信息

Osteoporos Int. 2025 Feb;36(2):245-254. doi: 10.1007/s00198-024-07309-9. Epub 2024 Dec 3.

Abstract

UNLABELLED

We analyzed the incidence of fractures and changes in bone mineral density and bone turnover markers in 264 patients who discontinued bisphosphonates. Fractures were recorded in 12.3%. Half were clinical vertebral fractures. We identified patients with a high-risk profile who should not discontinue treatment.

OBJECTIVE

The optimal length of bisphosphonate discontinuation is unknown, as is the type of patient who could benefit from this approach. The objectives of the study were to analyze, in clinical practice, the incidence of fractures and associated risk factors, changes in bone mineral density (BMD) and bone turnover markers (BTMs) after discontinuation of bisphosphonates.

METHODS

This observational retrospective study included 264 patients from 14 Spanish rheumatology departments. Postmenopausal women or men with osteoporosis received alendronate or risedronate for ≥ 5 years or zoledronate for ≥ 3 years and had discontinued treatment for ≥ 1 year or ≥ 2 years, respectively. Spinal X-rays were obtained before discontinuation and in suspected clinical vertebral fracture during follow-up. BMD and BTMs were determined before discontinuation and at different time points.

RESULTS

The mean discontinuation time was 2.7 (± 6.7) years. Thirty-two patients (12.3%) had 36 fractures, mainly clinical vertebral fractures. The main risk factor for fracture was a high-risk profile (femoral neck T-score ≤ -2.5 and/or a history of fracture and/or multiple fractures [≥ 5 years]) before discontinuation. At 12 months, 10.41% of patients with high-risk profile experienced a fracture, being 0.8% and 1.08% in moderate- and low-risk patients, respectively. Significant BMD loss at the femoral neck and total hip was detected, with duration of discontinuation being the key factor. PINP was the marker with the greatest changes.

CONCLUSIONS

We identified a profile of patients with osteoporosis who should not discontinue bisphosphonates, owing to the possibility of fractures, especially vertebral, which are already evident the first year after discontinuation.

摘要

未标注

我们分析了264例停用双膦酸盐类药物患者的骨折发生率、骨密度和骨转换标志物的变化。12.3%的患者发生了骨折。其中一半为临床椎体骨折。我们确定了不应停药的高危患者。

目的

双膦酸盐类药物停药的最佳时长尚不清楚,同样,能从这种方法中获益的患者类型也不明确。本研究的目的是在临床实践中分析骨折发生率及相关危险因素、双膦酸盐类药物停药后骨密度(BMD)和骨转换标志物(BTMs)的变化。

方法

这项观察性回顾性研究纳入了来自西班牙14个风湿病科的264例患者。绝经后骨质疏松女性或男性分别接受阿仑膦酸钠或利塞膦酸钠治疗≥5年或唑来膦酸治疗≥3年,且分别停药≥1年或≥2年。在停药前及随访期间疑似临床椎体骨折时拍摄脊柱X线片。在停药前及不同时间点测定骨密度和骨转换标志物。

结果

平均停药时间为2.7(±6.7)年。32例患者(12.3%)发生了36处骨折,主要为临床椎体骨折。骨折的主要危险因素是停药前的高危特征(股骨颈T值≤-2.5和/或有骨折病史和/或多发骨折[≥5年])。12个月时,高危患者中有10.41%发生骨折,中度和低度风险患者的骨折发生率分别为0.8%和1.08%。股骨颈和全髋骨密度有显著丢失,停药时长是关键因素。PINP是变化最大的标志物。

结论

我们确定了一类骨质疏松患者,因其有骨折风险,尤其是椎体骨折风险,在停药后第一年就已明显,所以不应停用双膦酸盐类药物。

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