Department of Osteology & Biomechanics, University Medical Center Hamburg-Eppendorf, D-22529 Hamburg, Germany.
Acta Biomater. 2010 Dec;6(12):4513-21. doi: 10.1016/j.actbio.2010.07.019. Epub 2010 Jul 21.
Strontium ranelate (SR) is one therapeutic option for reducing risk of fracture in osteoporosis. The effects of SR treatment on hydroxyapatite (HA) previously altered by bisphosphonate (BP) administration remain to be established. Patients who have received long-term BP treatment and present with persistent high fracture risk are of particular interest. Paired iliac crest biopsies from 15 patients post-BP therapy were subjected to a baseline biopsy and a follow-up biopsy after treatment with 2g SR day⁻¹ after either 6 months (n=5) or 12 months (n=10). Dual energy X-ray absorptiometry scans, serum parameters and biochemical markers were obtained. Quantitative backscattered electron imaging and energy-dispersive X-ray analyses combined with micro-X-ray fluorescence determinations were performed to observe any mineralization changes. Static 2-D histomorphometry was carried out to evaluate cellular and structural indices. After 6 months of SR treatment, increases in osteoid surface and strontium content were observed, but no other indices showed significant change. After 12 months of SR treatment, there was a significant increase in bone volume and trabecular thickness, and further increases in strontium content and backscattered signal intensity. These structural changes were accompanied by increased numbers of osteoblasts and increased osteoid surface and volume. Additionally, low bone resorption, as measured by beta-cross-laps, and a low number of osteoclasts were observed. SR treatment led to increased strontium content within the BP-HA nanocomposites and to increased osteoid indices and bone volume, which is indicative of newly formed bone, while osteoclasts were still suppressed. These data points suggest that SR might be considered as a therapeutic option for patients following long-term BP treatment.
雷奈酸锶(SR)是降低骨质疏松症骨折风险的一种治疗选择。 先前接受双膦酸盐(BP)治疗后对羟磷灰石(HA)的 SR 治疗效果仍有待确定。 特别关注那些长期接受 BP 治疗且持续存在高骨折风险的患者。 对 15 名接受 BP 治疗后的患者的髂嵴活检进行了基线活检和治疗后 6 个月(n=5)或 12 个月(n=10)后每天 2g SR 治疗的随访活检。 获得了双能 X 射线吸收法扫描,血清参数和生化标志物。 进行了定量背散射电子成像和能量色散 X 射线分析以及微 X 射线荧光测定,以观察任何矿化变化。 进行了静态 2-D 组织形态计量学以评估细胞和结构指数。 在 SR 治疗 6 个月后,观察到类骨质表面和锶含量增加,但其他指数没有明显变化。 在 SR 治疗 12 个月后,骨量和小梁厚度显著增加,锶含量和背散射信号强度进一步增加。 这些结构变化伴随着成骨细胞数量增加和类骨质表面和体积增加。 此外,β-交联环的低骨吸收和破骨细胞数量减少。 SR 治疗导致 BP-HA 纳米复合材料中的锶含量增加,类骨质指数和骨量增加,这表明形成了新骨,而破骨细胞仍受到抑制。 这些数据表明,SR 可被视为长期接受 BP 治疗的患者的治疗选择。