Gray Marena, Boughton Oliver, Wiles Crispin, Reinhard Christina, Vo Nghia T, Atwood Robert, Stavri Richard, Cobb Justin P, Hansen Ulrich, Abel Richard L
MSk Laboratory, Sir Michael Uren Hub, Department of Surgery and Cancer, Faculty of Medicine, Imperial College London, London, W12 0BZ, UK.
Warwick Medical School, University of Warwick, Coventry, CV4 7AL, UK.
Sci Rep. 2025 Aug 7;15(1):28894. doi: 10.1038/s41598-025-12494-6.
Microdefects, including microcracks and resorption trenches, may be important contributors to bone fragility. 3D microdefect morphology was imaged using synchrotron micro-CT to develop a classification system for investigating the relationship with bone mechanics and hip-fractures. Femoral heads from ageing hip-fracture patients (n = 5, 74-82 years) were compared to ageing non-fracture controls (n = 5, 72-84 years). Two trabecular cores were prepared from the chiasma; one was imaged using synchrotron micro-CT to measure microdefects and one was mechanically tested to measure tensile strength. Morphological and mechanical data were compared and correlated using Mann Whitney U test and Pearson's rank correlation. All the procedures performed were in accordance with the ethical standards of the Imperial College Tissue Bank (R13004) and the 1984 Declaration of Helsinki. Microdefects varied and were classified into four categories based on shape and measurable parameters. Hip-fracture donors exhibited significantly higher density of all microdefects (p < 0.05). Microdefect volume was strongly negatively correlated with ultimate tensile strength (p < 0.05) and stiffness (p < 0.05). Microdefects might contribute to loss of bone strength and fragility fracture via runaway resorption. Microcracks could promote focussed osteoclastic resorption and the formation of resorption pits which create stress risers leading to the re-formation of microcracks under continued load. CT-based classification methods should be used to explore the complex interaction between microdefects, metabolism, and bone fracture mechanics.
包括微裂纹和吸收沟在内的微缺陷可能是导致骨脆性的重要因素。利用同步加速器显微CT对三维微缺陷形态进行成像,以建立一个分类系统,用于研究其与骨力学和髋部骨折的关系。将老年髋部骨折患者(n = 5,74 - 82岁)的股骨头与老年非骨折对照组(n = 5,72 - 84岁)进行比较。从交叉处制备两个小梁核心;一个用同步加速器显微CT成像以测量微缺陷,另一个进行力学测试以测量拉伸强度。使用曼-惠特尼U检验和皮尔逊等级相关性对形态学和力学数据进行比较和关联。所有操作均符合帝国理工学院组织库(R13004)的伦理标准和1984年《赫尔辛基宣言》。微缺陷各不相同,并根据形状和可测量参数分为四类。髋部骨折供体的所有微缺陷密度均显著更高(p < 0.05)。微缺陷体积与极限拉伸强度(p < 0.05)和刚度(p < 0.05)呈强烈负相关。微缺陷可能通过失控吸收导致骨强度丧失和脆性骨折。微裂纹可促进集中的破骨细胞吸收和吸收坑的形成,这些吸收坑会产生应力集中点,导致在持续载荷下微裂纹重新形成。应使用基于CT的分类方法来探索微缺陷、代谢和骨折力学之间的复杂相互作用。