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Effect of size and location of simulated lytic lesions on the structural properties of human vertebral bodies, a micro-finite element study

Currently, the Spinal Instability Neoplastic Score system is used in clinics to evaluate the risk of fracture in patients with spinal metastases. This method, however, does not always provide a clear guideline due to the complexity in accounting for the effect of metastatic lesions on vertebral stab...

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Autores principales: Costa, M.C., Campello, L.B. Bresani, Ryan, M., Rochester, J., Viceconti, M., Dall'Ara, E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7292861/
https://www.ncbi.nlm.nih.gov/pubmed/32551335
http://dx.doi.org/10.1016/j.bonr.2020.100257
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author Costa, M.C.
Campello, L.B. Bresani
Ryan, M.
Rochester, J.
Viceconti, M.
Dall'Ara, E.
author_facet Costa, M.C.
Campello, L.B. Bresani
Ryan, M.
Rochester, J.
Viceconti, M.
Dall'Ara, E.
author_sort Costa, M.C.
collection PubMed
description Currently, the Spinal Instability Neoplastic Score system is used in clinics to evaluate the risk of fracture in patients with spinal metastases. This method, however, does not always provide a clear guideline due to the complexity in accounting for the effect of metastatic lesions on vertebral stability. The aim of this study was to use a validated micro Finite Element (microFE) modelling approach to analyse the effect of the size and location of lytic metastases on the mechanical properties of human vertebral bodies. Micro Computed Tomography based microFE models were generated with and without lytic lesions simulated as holes within a human vertebral body. Single and multiple lytic lesions were simulated with four different sizes and in five different locations. Bone was assumed homogenous, isotropic and linear elastic, and each vertebra was loaded in axial compression. It was observed that the size of lytic lesions was linearly related with the reduction in structural properties of the vertebral body (reduction of stiffness between 3% and 30% for lesion volume between 4% and 35%). The location of lytic lesions did not show a clear effect on predicted structural properties. Single or multiple lesions with the same volume provided similar results. Locally, there was a homogeneous distribution of axial principal strains among the models with and without lytic lesions. This study highlights the potential of microFE models to study the effect of lesions on the mechanical properties of the human vertebral body.
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spelling pubmed-72928612020-06-17 Effect of size and location of simulated lytic lesions on the structural properties of human vertebral bodies, a micro-finite element study Costa, M.C. Campello, L.B. Bresani Ryan, M. Rochester, J. Viceconti, M. Dall'Ara, E. Bone Rep Articles from the Special Issue on Computational Methods in Bone Research; Edited by Dr Penny Atkins and Dr Patrik Christen Currently, the Spinal Instability Neoplastic Score system is used in clinics to evaluate the risk of fracture in patients with spinal metastases. This method, however, does not always provide a clear guideline due to the complexity in accounting for the effect of metastatic lesions on vertebral stability. The aim of this study was to use a validated micro Finite Element (microFE) modelling approach to analyse the effect of the size and location of lytic metastases on the mechanical properties of human vertebral bodies. Micro Computed Tomography based microFE models were generated with and without lytic lesions simulated as holes within a human vertebral body. Single and multiple lytic lesions were simulated with four different sizes and in five different locations. Bone was assumed homogenous, isotropic and linear elastic, and each vertebra was loaded in axial compression. It was observed that the size of lytic lesions was linearly related with the reduction in structural properties of the vertebral body (reduction of stiffness between 3% and 30% for lesion volume between 4% and 35%). The location of lytic lesions did not show a clear effect on predicted structural properties. Single or multiple lesions with the same volume provided similar results. Locally, there was a homogeneous distribution of axial principal strains among the models with and without lytic lesions. This study highlights the potential of microFE models to study the effect of lesions on the mechanical properties of the human vertebral body. Elsevier 2020-03-09 /pmc/articles/PMC7292861/ /pubmed/32551335 http://dx.doi.org/10.1016/j.bonr.2020.100257 Text en © 2020 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Articles from the Special Issue on Computational Methods in Bone Research; Edited by Dr Penny Atkins and Dr Patrik Christen
Costa, M.C.
Campello, L.B. Bresani
Ryan, M.
Rochester, J.
Viceconti, M.
Dall'Ara, E.
Effect of size and location of simulated lytic lesions on the structural properties of human vertebral bodies, a micro-finite element study
title Effect of size and location of simulated lytic lesions on the structural properties of human vertebral bodies, a micro-finite element study
title_full Effect of size and location of simulated lytic lesions on the structural properties of human vertebral bodies, a micro-finite element study
title_fullStr Effect of size and location of simulated lytic lesions on the structural properties of human vertebral bodies, a micro-finite element study
title_full_unstemmed Effect of size and location of simulated lytic lesions on the structural properties of human vertebral bodies, a micro-finite element study
title_short Effect of size and location of simulated lytic lesions on the structural properties of human vertebral bodies, a micro-finite element study
title_sort effect of size and location of simulated lytic lesions on the structural properties of human vertebral bodies, a micro-finite element study
topic Articles from the Special Issue on Computational Methods in Bone Research; Edited by Dr Penny Atkins and Dr Patrik Christen
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7292861/
https://www.ncbi.nlm.nih.gov/pubmed/32551335
http://dx.doi.org/10.1016/j.bonr.2020.100257
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