MSk Laboratory, Sir Michael Uren Hub, Department of Surgery and Cancer, Faculty of Medicine, Imperial College London, London, W12 0BZ, UK.
Department of Mechanical Engineering, Faculty of Engineering, Imperial College London, London, SW7 2AZ, UK.
Curr Osteoporos Rep. 2021 Jun;19(3):318-326. doi: 10.1007/s11914-021-00678-8. Epub 2021 Apr 20.
Bone matrix exhibits great complexity in its composition, structure and mechanics. Here, we provide a review of recent research articles and appraise the evidence that bone matrix quality is clinically important and possibly targetable for fracture prevention.
Deformation of mineralised collagen fibrils determines bone fracture mechanics. Slipping and separation at the mineral-fibril and fibril-fibril interfaces, respectively, are the structural mechanisms for plastic deformation and microcrack nucleation. Existing technologies for assessing bone tissue in vivo cannot measure matrix structure or fracture mechanics but have shown limited use in clinical settings for identifying fragility or following treatment outcomes based on composition. Matrix is biomechanically and clinically important, but the knowledge has not translated into clinical practice. The structural mechanisms by which a load is transferred from mineralised collagen fibrils to the whole bone via microcracking have been proven too complex to measure in vivo. The mineral-fibril or fibril-fibril interfaces might be suitable targets for diagnosing fragility or delivering molecules that reduce fracture risk by strengthening the mineral bonds while maintaining flexibility in the fibrils.
骨基质在组成、结构和力学上具有极大的复杂性。在这里,我们对最近的研究文章进行综述,并评估骨基质质量具有临床重要性且可能成为预防骨折的靶点的证据。
矿化胶原纤维的变形决定了骨的力学性能。矿化纤维和纤维之间的滑动和分离分别是塑性变形和微裂纹成核的结构机制。现有的评估活体骨组织的技术无法测量基质结构或力学性能,但在临床上用于识别脆弱性或根据组成跟踪治疗结果的用途有限。基质在生物力学和临床上都很重要,但这方面的知识尚未转化为临床实践。通过微裂纹将负载从矿化胶原纤维传递到整个骨骼的结构机制过于复杂,无法在体内进行测量。矿化纤维或纤维之间的界面可能是诊断脆弱性或通过增强矿物质结合力同时保持纤维柔韧性来降低骨折风险的分子的合适靶点。