Biomechanical and microstructural evaluation of newly formed bone following static/dynamic bone growth modulation in an immature animal model.

在未成熟动物模型中静态/动态骨生长调节后新形成骨的生物力学和微观结构评估。

• 批准号: RGPIN-2014-06364
• 负责人: Villemure, Isabelle
• 金额: $ 2.4万
• 依托单位: École Polytechnique de Montréal
• 依托单位国家: 加拿大
• 项目类别: Discovery Grants Program - Individual
• 财政年份: 2017
• 资助国家: 加拿大
• 起止时间: 2017-01-01 至 2018-12-31
• 项目状态: 已结题
• 来源: https://www.nserc-crsng.gc.ca/ase-oro/Details-Detailles_eng.asp?id=638489
• 关键词: Biomechanical; microstructural; evaluation; newly; formed

CONTEXT: Fusionless medical devices are one of the most promising treatments of pediatric spinal deformities due to their capacity to prevent spinal arthrodesis and repetitive/staged surgeries as in current instrumentation treatments. They are based on the mechanical modulation of bone growth, a process by which forces can modulate bone growth rate. To correct the deformities, these implants restrict unilateral bone growth on the convexity of the spinal curvature by locally increasing compressive stress over vertebral growth plates, where bone growth occurs. Up to now, experimental studies have mainly focused on the effects of static and/or dynamic compression on the growth plates, while the impact of growth modulation on the quality of « newly formed bone », emerging below the growth plate, has not been characterized neither in its microarchitecture nor its biomechanics. With rapidly increasing interest and developments in these fusionless implants, it becomes very important to identify which loading parameters transferred by these devices will impact on the quality of newly formed bone to further guide their design for the treatment of pediatric skeletal deformities. OBJECTIVES AND METHODOLOGY: This program comprises two main research objectives: (I) to characterize the effects of in vivo static vs dynamic growth modulation on the biology and microstructure of newly formed trabecular bone; (II) to evaluate the effects of in vivo static vs dynamic growth modulation on the biomechanical properties of newly formed trabecular bone. As a logical extension of previous work on growth plate mechanobiology, the effects of finely controlled static or cyclic loads on newly formed bone will be investigated using our rat tail model. Static or dynamic compression will be applied using our air-driven device implanted on the rat tail to load the 7th caudal vertebra. In vivo monitoring of newly formed bone microarchitecture will be done using micro-CT imaging to evaluate typical trabecular and cortical parameters. A finite element approach, based on extracted micro-CT geometrical and mechanical data, will be developed and used to non-destructively estimate the mechanical properties of the newly formed bone. The composition and biology of newly formed bone will also be characterized using immunohistochemistry/staining techniques for osteogenesis markers as well as labeling techniques to evaluate bone growth rates. Statistical analyses will allow comparing the impacts of static/dynamic growth modulation on the quality of newly formed bone in terms of microstructure, composition and biomechanics.NOVELTY AND EXPECTED SIGNIFICANCE: Current treatments of spinal deformities, such as scoliosis, involve invasive surgical instrumentation and vertebral fusion. Recent advances in fusionless techniques of the spine, by means of local mechanical modulation of bone growth, have shown great promise in the treatment of these progressive spinal deformities. They present less surgical risks and complications than the traditional surgery and preserve spinal growth, spinal motion and function. It is clear that a better understanding of the factors involved in bone growth modulation are essential to guide and improve the design of novel fusionless techniques, which could be designed more or less constrained to transmit either static or dynamic loads. However, it still is not clear at the moment what loading parameters would be efficient and non-damaging for bone growth modulation. The knowledge that will result from the proposed research program will be of great value for the design of novel fusionless implants for pediatric skeletal deformities, not only in the spine but also in the lower/upper limb deformities.

背景：非融合医疗器械是儿科脊柱畸形最有前途的治疗方法之一，因为它们能够防止脊柱关节固定术和重复/分期手术，如当前的内固定治疗。它们基于骨生长的机械调节，通过该过程力可以调节骨生长速率。为了矫正畸形，这些植入物通过局部增加椎骨生长板上的压缩应力来限制脊柱弯曲凸面上的单侧骨生长，其中骨生长发生在椎骨生长板上。到目前为止，实验研究主要集中在静态和/或动态压缩对生长板的影响上，而生长调节对生长板下出现的“新形成的骨”质量的影响尚未在其微结构或生物力学方面进行表征。随着对这些非融合植入物的兴趣和发展迅速增加，确定这些器械传递的哪些载荷参数将影响新形成骨的质量，以进一步指导其治疗儿科骨骼畸形的设计变得非常重要。动机和方法：该计划包括两个主要研究目标：（I）表征体内静态与动态生长调节对新形成的骨小梁的生物学和微观结构的影响;（II）评价体内静态与动态生长调节对新形成的骨小梁的生物力学特性的影响。作为生长板机械生物学以前的工作的逻辑延伸，精细控制的静态或循环载荷对新形成的骨的影响将使用我们的大鼠尾巴模型进行研究。将使用我们植入大鼠尾部的气动装置施加静态或动态压缩，以加载第7尾椎。将使用微CT成像对新形成的骨微结构进行体内监测，以评价典型的骨小梁和皮质参数。一种有限元方法，提取的micro-CT几何和力学数据的基础上，将被开发和用于非破坏性地估计新形成的骨的力学性能。还将使用成骨标志物的免疫组织化学/染色技术以及评价骨生长速率的标记技术表征新形成骨的组成和生物学。统计分析将允许比较静态/动态生长调制对新形成的骨的微观结构，成分和生物力学方面的质量的影响。新奇和预期的意义：目前的治疗脊柱畸形，如脊柱侧凸，涉及侵入性手术器械和椎体融合。脊柱非融合技术的最新进展，通过局部机械调节骨生长，在治疗这些进行性脊柱畸形方面显示出巨大的前景。与传统手术相比，它们具有更低的手术风险和并发症，并保留了脊柱生长，脊柱运动和功能。很明显，更好地理解骨生长调节中涉及的因素对于指导和改进新型非融合技术的设计至关重要，该技术可以或多或少地被设计为限制传递静态或动态载荷。然而，目前尚不清楚什么样的加载参数对于骨生长调节是有效和非损伤的。从拟议的研究计划中获得的知识将对设计用于儿科骨骼畸形的新型非融合植入物具有重要价值，不仅在脊柱中，而且在下肢/上肢畸形中。