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Comparison of interpolation methods of predominant cardiomyocyte orientation from in vivo and ex vivo cardiac diffusion tensor imaging data
Cardiac electrophysiology and cardiac mechanics both depend on the average cardiomyocyte long‐axis orientation. In the realm of personalized medicine, knowledge of the patient‐specific changes in cardiac microstructure plays a crucial role. Patient‐specific computational modelling has emerged as a t...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9285076/ https://www.ncbi.nlm.nih.gov/pubmed/34964179 http://dx.doi.org/10.1002/nbm.4667 |
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author | Stimm, Johanna Guenthner, Christian Kozerke, Sebastian Stoeck, Christian T. |
author_facet | Stimm, Johanna Guenthner, Christian Kozerke, Sebastian Stoeck, Christian T. |
author_sort | Stimm, Johanna |
collection | PubMed |
description | Cardiac electrophysiology and cardiac mechanics both depend on the average cardiomyocyte long‐axis orientation. In the realm of personalized medicine, knowledge of the patient‐specific changes in cardiac microstructure plays a crucial role. Patient‐specific computational modelling has emerged as a tool to better understand disease progression. In vivo cardiac diffusion tensor imaging (cDTI) is a vital tool to non‐destructively measure the average cardiomyocyte long‐axis orientation in the heart. However, cDTI suffers from long scan times, rendering volumetric, high‐resolution acquisitions challenging. Consequently, interpolation techniques are needed to populate bio‐mechanical models with patient‐specific average cardiomyocyte long‐axis orientations. In this work, we compare five interpolation techniques applied to in vivo and ex vivo porcine input data. We compare two tensor interpolation approaches, one rule‐based approximation, and two data‐driven, low‐rank models. We demonstrate the advantage of tensor interpolation techniques, resulting in lower interpolation errors than do low‐rank models and rule‐based methods adapted to cDTI data. In an ex vivo comparison, we study the influence of three imaging parameters that can be traded off against acquisition time: in‐plane resolution, signal to noise ratio, and number of acquired short‐axis imaging slices. |
format | Online Article Text |
id | pubmed-9285076 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92850762022-07-15 Comparison of interpolation methods of predominant cardiomyocyte orientation from in vivo and ex vivo cardiac diffusion tensor imaging data Stimm, Johanna Guenthner, Christian Kozerke, Sebastian Stoeck, Christian T. NMR Biomed Research Articles Cardiac electrophysiology and cardiac mechanics both depend on the average cardiomyocyte long‐axis orientation. In the realm of personalized medicine, knowledge of the patient‐specific changes in cardiac microstructure plays a crucial role. Patient‐specific computational modelling has emerged as a tool to better understand disease progression. In vivo cardiac diffusion tensor imaging (cDTI) is a vital tool to non‐destructively measure the average cardiomyocyte long‐axis orientation in the heart. However, cDTI suffers from long scan times, rendering volumetric, high‐resolution acquisitions challenging. Consequently, interpolation techniques are needed to populate bio‐mechanical models with patient‐specific average cardiomyocyte long‐axis orientations. In this work, we compare five interpolation techniques applied to in vivo and ex vivo porcine input data. We compare two tensor interpolation approaches, one rule‐based approximation, and two data‐driven, low‐rank models. We demonstrate the advantage of tensor interpolation techniques, resulting in lower interpolation errors than do low‐rank models and rule‐based methods adapted to cDTI data. In an ex vivo comparison, we study the influence of three imaging parameters that can be traded off against acquisition time: in‐plane resolution, signal to noise ratio, and number of acquired short‐axis imaging slices. John Wiley and Sons Inc. 2021-12-29 2022-05 /pmc/articles/PMC9285076/ /pubmed/34964179 http://dx.doi.org/10.1002/nbm.4667 Text en © 2021 The Authors. NMR in Biomedicine published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Articles Stimm, Johanna Guenthner, Christian Kozerke, Sebastian Stoeck, Christian T. Comparison of interpolation methods of predominant cardiomyocyte orientation from in vivo and ex vivo cardiac diffusion tensor imaging data |
title | Comparison of interpolation methods of predominant cardiomyocyte orientation from in vivo and ex vivo cardiac diffusion tensor imaging data |
title_full | Comparison of interpolation methods of predominant cardiomyocyte orientation from in vivo and ex vivo cardiac diffusion tensor imaging data |
title_fullStr | Comparison of interpolation methods of predominant cardiomyocyte orientation from in vivo and ex vivo cardiac diffusion tensor imaging data |
title_full_unstemmed | Comparison of interpolation methods of predominant cardiomyocyte orientation from in vivo and ex vivo cardiac diffusion tensor imaging data |
title_short | Comparison of interpolation methods of predominant cardiomyocyte orientation from in vivo and ex vivo cardiac diffusion tensor imaging data |
title_sort | comparison of interpolation methods of predominant cardiomyocyte orientation from in vivo and ex vivo cardiac diffusion tensor imaging data |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9285076/ https://www.ncbi.nlm.nih.gov/pubmed/34964179 http://dx.doi.org/10.1002/nbm.4667 |
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