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Liquid crystal phantom for validation of microscopic diffusion anisotropy measurements on clinical MRI systems

PURPOSE: To develop a phantom for validating MRI pulse sequences and data processing methods to quantify microscopic diffusion anisotropy in the human brain. METHODS: Using a liquid crystal consisting of water, detergent, and hydrocarbon, we designed a 0.5‐L spherical phantom showing the theoretical...

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Autores principales: Nilsson, Markus, Larsson, Johan, Lundberg, Dan, Szczepankiewicz, Filip, Witzel, Thomas, Westin, Carl‐Fredrik, Bryskhe, Karin, Topgaard, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5756689/
https://www.ncbi.nlm.nih.gov/pubmed/28686785
http://dx.doi.org/10.1002/mrm.26814
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author Nilsson, Markus
Larsson, Johan
Lundberg, Dan
Szczepankiewicz, Filip
Witzel, Thomas
Westin, Carl‐Fredrik
Bryskhe, Karin
Topgaard, Daniel
author_facet Nilsson, Markus
Larsson, Johan
Lundberg, Dan
Szczepankiewicz, Filip
Witzel, Thomas
Westin, Carl‐Fredrik
Bryskhe, Karin
Topgaard, Daniel
author_sort Nilsson, Markus
collection PubMed
description PURPOSE: To develop a phantom for validating MRI pulse sequences and data processing methods to quantify microscopic diffusion anisotropy in the human brain. METHODS: Using a liquid crystal consisting of water, detergent, and hydrocarbon, we designed a 0.5‐L spherical phantom showing the theoretically highest possible degree of microscopic anisotropy. Data were acquired on the Connectome scanner using echo‐planar imaging signal readout and diffusion encoding with axisymmetric b‐tensors of varying magnitude, anisotropy, and orientation. The mean diffusivity, fractional anisotropy (FA), and microscopic FA (µFA) parameters were estimated. RESULTS: The phantom was observed to have values of mean diffusivity similar to brain tissue, and relaxation times compatible with echo‐planar imaging echo times on the order of 100 ms. The estimated values of µFA were at the theoretical maximum of 1.0, whereas the values of FA spanned the interval from 0.0 to 0.8 as a result of varying orientational order of the anisotropic domains within each voxel. CONCLUSIONS: The proposed phantom can be manufactured by mixing three widely available chemicals in volumes comparable to a human head. The acquired data are in excellent agreement with theoretical predictions, showing that the phantom is ideal for validating methods for measuring microscopic diffusion anisotropy on clinical MRI systems. Magn Reson Med 79:1817–1828, 2018. © 2017 The Authors Magnetic Resonance in Medicine published by Wiley Periodicals, Inc. on behalf of International Society for Magnetic Resonance in Medicine. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
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spelling pubmed-57566892018-02-16 Liquid crystal phantom for validation of microscopic diffusion anisotropy measurements on clinical MRI systems Nilsson, Markus Larsson, Johan Lundberg, Dan Szczepankiewicz, Filip Witzel, Thomas Westin, Carl‐Fredrik Bryskhe, Karin Topgaard, Daniel Magn Reson Med Full Papers—Hardware and Instrumentation PURPOSE: To develop a phantom for validating MRI pulse sequences and data processing methods to quantify microscopic diffusion anisotropy in the human brain. METHODS: Using a liquid crystal consisting of water, detergent, and hydrocarbon, we designed a 0.5‐L spherical phantom showing the theoretically highest possible degree of microscopic anisotropy. Data were acquired on the Connectome scanner using echo‐planar imaging signal readout and diffusion encoding with axisymmetric b‐tensors of varying magnitude, anisotropy, and orientation. The mean diffusivity, fractional anisotropy (FA), and microscopic FA (µFA) parameters were estimated. RESULTS: The phantom was observed to have values of mean diffusivity similar to brain tissue, and relaxation times compatible with echo‐planar imaging echo times on the order of 100 ms. The estimated values of µFA were at the theoretical maximum of 1.0, whereas the values of FA spanned the interval from 0.0 to 0.8 as a result of varying orientational order of the anisotropic domains within each voxel. CONCLUSIONS: The proposed phantom can be manufactured by mixing three widely available chemicals in volumes comparable to a human head. The acquired data are in excellent agreement with theoretical predictions, showing that the phantom is ideal for validating methods for measuring microscopic diffusion anisotropy on clinical MRI systems. Magn Reson Med 79:1817–1828, 2018. © 2017 The Authors Magnetic Resonance in Medicine published by Wiley Periodicals, Inc. on behalf of International Society for Magnetic Resonance in Medicine. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. John Wiley and Sons Inc. 2017-07-07 2018-03 /pmc/articles/PMC5756689/ /pubmed/28686785 http://dx.doi.org/10.1002/mrm.26814 Text en © 2017 The Authors Magnetic Resonance in Medicine published by Wiley Periodicals, Inc. on behalf of International Society for Magnetic Resonance in Medicine This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Full Papers—Hardware and Instrumentation
Nilsson, Markus
Larsson, Johan
Lundberg, Dan
Szczepankiewicz, Filip
Witzel, Thomas
Westin, Carl‐Fredrik
Bryskhe, Karin
Topgaard, Daniel
Liquid crystal phantom for validation of microscopic diffusion anisotropy measurements on clinical MRI systems
title Liquid crystal phantom for validation of microscopic diffusion anisotropy measurements on clinical MRI systems
title_full Liquid crystal phantom for validation of microscopic diffusion anisotropy measurements on clinical MRI systems
title_fullStr Liquid crystal phantom for validation of microscopic diffusion anisotropy measurements on clinical MRI systems
title_full_unstemmed Liquid crystal phantom for validation of microscopic diffusion anisotropy measurements on clinical MRI systems
title_short Liquid crystal phantom for validation of microscopic diffusion anisotropy measurements on clinical MRI systems
title_sort liquid crystal phantom for validation of microscopic diffusion anisotropy measurements on clinical mri systems
topic Full Papers—Hardware and Instrumentation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5756689/
https://www.ncbi.nlm.nih.gov/pubmed/28686785
http://dx.doi.org/10.1002/mrm.26814
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