Biomechanical effects of defect size and location on vertebral fracture

椎体骨折中缺陷大小和位置的生物力学效应

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Abstract

PURPOSE: Investigating the effect of metastatic lesions on the load-bearing capacity of the spinal column is essential for identifying appropriate interventions for patients. Most studies on the effects of tumor size and location on vertebral fractures are computational, with limited experimental data available. Furthermore, it remains unclear which parameters are most critical for assessing fracture risk in metastatic spines. The purpose of the current study was to investigate the effect of lesion size and location on fracture characteristics of the vertebral body and to find contributing factors associated with vertebral fractures. METHODS: Human cadaveric spine segments were dissected from fresh frozen torsos and divided into three groups: intact, central defects affecting only trabecular bones, and anterior defects affecting both cortical and trabecular bones. Computed tomography imaging was performed to measure the geometry and Hounsfield Unit (HU) values and then, these specimens were mechanically tested to failure to record vertebral fracture forces. RESULTS: Compared to the intact specimens (2092 kPa), the average fracture strength in the defect groups were reduced by at least 750 kPa with a defect size as small as 25% of the cross-sectional area (CSA) or 9% of the volume (p=0.0097). Tumor location did not significantly affect vertebral fracture forces (p=0.77), as both locations primarily involved trabecular bone. CONCLUSION: The results of this study suggest that the vertebral body becomes significantly weaker even with simulated lytic defects involving as little as approximately 9% of the vertebral volume or 25% of the vertebral cross-sectional area (CSA). This degree of bone involvement may represent a new biomechanical threshold for assessing fracture risk in metastatic spines with bone loss. These findings underscore the importance of proactive assessment and potential early intervention in patients with small vertebral lytic lesions-particularly in individuals already at elevated risk of vertebral fracture due to conditions such as osteoporosis.

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