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唑来膦酸对肌腱-骨愈合的负面影响。

Negative effect of zoledronic acid on tendon-to-bone healing.

机构信息

a Division of Orthopedic Surgery , Oslo University Hospital (OUS) , Norway.

b Institute of Clinical Medicine, Faculty of Medicine, University of Oslo (UIO).

出版信息

Acta Orthop. 2018 Jun;89(3):360-366. doi: 10.1080/17453674.2018.1440189. Epub 2018 Mar 1.

Abstract

Background and purpose - Outcome after ligament reconstruction or tendon repair depends on secure tendon-to-bone healing. Increased osteoclastic activity resulting in local bone loss may contribute to delayed healing of the tendon-bone interface. The objective of this study was to evaluate the effect of the bisphosphonate zoledronic acid (ZA) on tendon-to-bone healing. Methods - Wistar rats (n = 92) had their right Achilles tendon cut proximally, pulled through a bone tunnel in the distal tibia and sutured anteriorly. After 1 week animals were randomized to receive a single dose of ZA (0.1 mg/kg IV) or control. Healing was evaluated at 3 and 6 weeks by mechanical testing, dual-energy X-ray absorptiometry and histology including immunohistochemical staining of osteoclasts. Results - ZA treatment resulted in 19% (95% CI 5-33%) lower pullout strength and 43% (95% CI 14-72%) lower stiffness of the tendon-bone interface, compared with control (2-way ANOVA; p = 0.009, p = 0.007). Administration of ZA did not affect bone mineral density (BMD) or bone mineral content (BMC). Histological analyses did not reveal differences in callus formation or osteoclasts between the study groups. Interpretation - ZA reduced pullout strength and stiffness of the tendon-bone interface. The study does not provide support for ZA as adjuvant treatment in tendon-to-bone healing.

摘要

背景与目的-韧带重建或肌腱修复后的结果取决于肌腱与骨的牢固愈合。破骨细胞活性增加导致局部骨丢失可能会影响肌腱与骨界面的愈合延迟。本研究的目的是评估双膦酸盐唑来膦酸(ZA)对肌腱与骨愈合的影响。方法- Wistar 大鼠(n = 92)将其右侧跟腱近端切断,穿过胫骨远端的骨隧道,并在前侧缝合。1 周后,动物随机接受单次 ZA(0.1mg/kg IV)或对照治疗。通过机械测试、双能 X 射线吸收法和组织学(包括破骨细胞的免疫组织化学染色)评估 3 周和 6 周时的愈合情况。结果-ZA 治疗组与对照组相比,肌腱与骨界面的拔出强度降低 19%(95%CI 5-33%),刚度降低 43%(95%CI 14-72%)(2 路 ANOVA;p = 0.009,p = 0.007)。ZA 给药并不影响骨密度(BMD)或骨矿物质含量(BMC)。组织学分析未显示研究组之间在骨痂形成或破骨细胞方面存在差异。结论-ZA 降低了肌腱与骨界面的拔出强度和刚度。本研究不支持 ZA 作为肌腱与骨愈合的辅助治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68d8/6055777/940605c35f10/iort-89-360.F01.jpg

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