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A generative model of hyperelastic strain energy density functions for multiple tissue brain deformation

PURPOSE: Estimation of brain deformation is crucial during neurosurgery. Whilst mechanical characterisation captures stress–strain relationships of tissue, biomechanical models are limited by experimental conditions. This results in variability reported in the literature. The aim of this work was to...

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Autores principales: Granados, Alejandro, Perez-Garcia, Fernando, Schweiger, Martin, Vakharia, Vejay, Vos, Sjoerd B., Miserocchi, Anna, McEvoy, Andrew W., Duncan, John S., Sparks, Rachel, Ourselin, Sébastien
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7822772/
https://www.ncbi.nlm.nih.gov/pubmed/33165705
http://dx.doi.org/10.1007/s11548-020-02284-y
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author Granados, Alejandro
Perez-Garcia, Fernando
Schweiger, Martin
Vakharia, Vejay
Vos, Sjoerd B.
Miserocchi, Anna
McEvoy, Andrew W.
Duncan, John S.
Sparks, Rachel
Ourselin, Sébastien
author_facet Granados, Alejandro
Perez-Garcia, Fernando
Schweiger, Martin
Vakharia, Vejay
Vos, Sjoerd B.
Miserocchi, Anna
McEvoy, Andrew W.
Duncan, John S.
Sparks, Rachel
Ourselin, Sébastien
author_sort Granados, Alejandro
collection PubMed
description PURPOSE: Estimation of brain deformation is crucial during neurosurgery. Whilst mechanical characterisation captures stress–strain relationships of tissue, biomechanical models are limited by experimental conditions. This results in variability reported in the literature. The aim of this work was to demonstrate a generative model of strain energy density functions can estimate the elastic properties of tissue using observed brain deformation. METHODS: For the generative model a Gaussian Process regression learns elastic potentials from 73 manuscripts. We evaluate the use of neo-Hookean, Mooney–Rivlin and 1-term Ogden meta-models to guarantee stability. Single and multiple tissue experiments validate the ability of our generative model to estimate tissue properties on a synthetic brain model and in eight temporal lobe resection cases where deformation is observed between pre- and post-operative images. RESULTS: Estimated parameters on a synthetic model are close to the known reference with a root-mean-square error (RMSE) of 0.1 mm and 0.2 mm between surface nodes for single and multiple tissue experiments. In clinical cases, we were able to recover brain deformation from pre- to post-operative images reducing RMSE of differences from 1.37 to 1.08 mm on the ventricle surface and from 5.89 to 4.84 mm on the resection cavity surface. CONCLUSION: Our generative model can capture uncertainties related to mechanical characterisation of tissue. When fitting samples from elastography and linear studies, all meta-models performed similarly. The Ogden meta-model performed the best on hyperelastic studies. We were able to predict elastic parameters in a reference model on a synthetic phantom. However, deformation observed in clinical cases is only partly explained using our generative model. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s11548-020-02284-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-78227722021-01-28 A generative model of hyperelastic strain energy density functions for multiple tissue brain deformation Granados, Alejandro Perez-Garcia, Fernando Schweiger, Martin Vakharia, Vejay Vos, Sjoerd B. Miserocchi, Anna McEvoy, Andrew W. Duncan, John S. Sparks, Rachel Ourselin, Sébastien Int J Comput Assist Radiol Surg Original Article PURPOSE: Estimation of brain deformation is crucial during neurosurgery. Whilst mechanical characterisation captures stress–strain relationships of tissue, biomechanical models are limited by experimental conditions. This results in variability reported in the literature. The aim of this work was to demonstrate a generative model of strain energy density functions can estimate the elastic properties of tissue using observed brain deformation. METHODS: For the generative model a Gaussian Process regression learns elastic potentials from 73 manuscripts. We evaluate the use of neo-Hookean, Mooney–Rivlin and 1-term Ogden meta-models to guarantee stability. Single and multiple tissue experiments validate the ability of our generative model to estimate tissue properties on a synthetic brain model and in eight temporal lobe resection cases where deformation is observed between pre- and post-operative images. RESULTS: Estimated parameters on a synthetic model are close to the known reference with a root-mean-square error (RMSE) of 0.1 mm and 0.2 mm between surface nodes for single and multiple tissue experiments. In clinical cases, we were able to recover brain deformation from pre- to post-operative images reducing RMSE of differences from 1.37 to 1.08 mm on the ventricle surface and from 5.89 to 4.84 mm on the resection cavity surface. CONCLUSION: Our generative model can capture uncertainties related to mechanical characterisation of tissue. When fitting samples from elastography and linear studies, all meta-models performed similarly. The Ogden meta-model performed the best on hyperelastic studies. We were able to predict elastic parameters in a reference model on a synthetic phantom. However, deformation observed in clinical cases is only partly explained using our generative model. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s11548-020-02284-y) contains supplementary material, which is available to authorized users. Springer International Publishing 2020-11-09 2021 /pmc/articles/PMC7822772/ /pubmed/33165705 http://dx.doi.org/10.1007/s11548-020-02284-y Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Original Article
Granados, Alejandro
Perez-Garcia, Fernando
Schweiger, Martin
Vakharia, Vejay
Vos, Sjoerd B.
Miserocchi, Anna
McEvoy, Andrew W.
Duncan, John S.
Sparks, Rachel
Ourselin, Sébastien
A generative model of hyperelastic strain energy density functions for multiple tissue brain deformation
title A generative model of hyperelastic strain energy density functions for multiple tissue brain deformation
title_full A generative model of hyperelastic strain energy density functions for multiple tissue brain deformation
title_fullStr A generative model of hyperelastic strain energy density functions for multiple tissue brain deformation
title_full_unstemmed A generative model of hyperelastic strain energy density functions for multiple tissue brain deformation
title_short A generative model of hyperelastic strain energy density functions for multiple tissue brain deformation
title_sort generative model of hyperelastic strain energy density functions for multiple tissue brain deformation
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7822772/
https://www.ncbi.nlm.nih.gov/pubmed/33165705
http://dx.doi.org/10.1007/s11548-020-02284-y
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