Moran Meghan M, Wilson Brittany M, Ross Ryan D, Virdi Amarjit S, Sumner Dale Rick
Department of Cell & Molecular Medicine, Rush University Medical Center, Chicago, Illinois.
J Orthop Res. 2017 Dec;35(12):2595-2605. doi: 10.1002/jor.23619. Epub 2017 Jun 28.
We completed a systematic literature review of in vivo animal models that use arthrotomy-based methods to study particle-induced peri-implant osteolysis. The purpose of the review was to characterize the models developed to date, to determine the questions addressed, to assess scientific rigor and transparency, and to identify gaps in knowledge. We probed three literature databases (Medline, Embase, and Scopus) and found 77 manuscripts that fit the search parameters. In the most recent 10 years, researchers mainly used rat and mouse models, whereas in the previous 20 years, large animal, canine, and rabbit models were more common. The studies have demonstrated several pathophysiology pathways, including macrophage migration, particle phagocytosis, increased local production of cytokines and lysosomal enzymes, elevated bone resorption, and suppressed bone formation. The effect of variation in particle characteristics and concentration received limited attention with somewhat mixed findings. Particle contamination by endotoxin was shown to exacerbate peri-implant osteolysis. The possibility of early diagnosis was demonstrated through imaging and biomarker approaches. Several studies showed that both local and systemic delivery of bisphosphonates inhibits the development of particle-induced osteolysis. Other methods of inhibiting osteolysis include the use of anabolic agents and altering the implant design. Few studies examined non-surgical rescue of loosened implants, with conflicting results with alendronate. We found that the manuscripts often lacked the methodological detail now advocated by the ARRIVE guidelines, suggesting that improvement in reporting would be useful to maximize rigor and transparency. © 2017 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 35:2595-2605, 2017.
我们完成了一项关于体内动物模型的系统文献综述,这些模型采用基于关节切开术的方法来研究颗粒诱导的种植体周围骨溶解。该综述的目的是描述迄今为止所开发的模型,确定所解决的问题,评估科学严谨性和透明度,并找出知识空白。我们检索了三个文献数据库(Medline、Embase和Scopus),发现77篇符合检索参数的手稿。在最近10年里,研究人员主要使用大鼠和小鼠模型,而在之前的20年里,大型动物、犬类和兔类模型更为常见。这些研究已经证明了几种病理生理途径,包括巨噬细胞迁移、颗粒吞噬、细胞因子和溶酶体酶的局部产生增加、骨吸收增加以及骨形成受抑制。颗粒特性和浓度变化的影响受到的关注有限,研究结果也有些参差不齐。内毒素引起的颗粒污染被证明会加剧种植体周围骨溶解。通过成像和生物标志物方法证明了早期诊断的可能性。几项研究表明,双膦酸盐的局部和全身给药均能抑制颗粒诱导的骨溶解的发展。其他抑制骨溶解的方法包括使用合成代谢药物和改变种植体设计。很少有研究考察松动种植体的非手术挽救方法,阿仑膦酸钠的研究结果相互矛盾。我们发现这些手稿往往缺乏现在ARRIVE指南所倡导的方法学细节,这表明改进报告将有助于最大限度地提高严谨性和透明度。©2017骨科学研究协会。由Wiley Periodicals, Inc.出版。《矫形外科学研究》35:2595 - 2605, 2017。