Evidence map›Paper›PMID 41878637›Full record

ArticleJournal of medical and biological engineering2025

Biomechanical effects of defect size and location on vertebral fracture.

Asghar Rezaei, Areonna Schreiber, Babak Dashtdar, Cameron Aubert, Abdelrahman M Hamouda, Benjamin Elder, Kenton Kaufman, Lichun Lu

Abstract read
In one paragraph

Article in Journal of medical and biological engineering, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Asghar RezaeiDepartment of Physiology and Biomedical Engineering, Mayo Clinic, Rochester, MN.
Areonna SchreiberDepartment of Physiology and Biomedical Engineering, Mayo Clinic, Rochester, MN.
Babak DashtdarDepartment of Physiology and Biomedical Engineering, Mayo Clinic, Rochester, MN.
Cameron AubertDepartment of Neurologic Surgery, Mayo Clinic, Rochester, MN.
Abdelrahman M HamoudaDepartment of Neurologic Surgery, Mayo Clinic, Rochester, MN.
Benjamin ElderDepartment of Neurologic Surgery, Mayo Clinic, Rochester, MN.
Kenton KaufmanDepartment of Orthopedic Surgery, Mayo Clinic, Rochester, MN.
Lichun LuDepartment of Physiology and Biomedical Engineering, Mayo Clinic, Rochester, MN.

Funding

Mayo Clinic Center for Clinical and Translational Science (CCaTS UL1 Supplement - Dr. Timothy Curry)UL1TR002377 · NCATS · MAYO CLINIC ROCHESTER · PI VESNA D GAROVIC · 2017 to 2026
$78.4M
Metastatic Spine Tumors: Minimally Invasive Fracture Risk Analysis and Treatment - MasterR01AR056212 · NIAMS · MAYO CLINIC ROCHESTER · PI Benjamin D Elder, Lichun Lu · 2008 to 2026
$6.2M
A patient-specific computational technique to predict spine injury risks associated with physical activitiesK25AG068368 · NIA · MAYO CLINIC ROCHESTER · PI REZAEI, ASGHAR · 2021 to 2025
$737k
NCATS NIH HHS UL1 TR002377NIAMS NIH HHS R01 AR056212NIA NIH HHS K25 AG068368
6 · The paper itself

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.

Indexed as

biomechanics of spinelesion size and locationVertebral fracture

Identifiers

PMID41878637
PMCPMC13007978

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.