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Multi-Compartment T2 Relaxometry Using a Spatially Constrained Multi-Gaussian Model
The brain’s myelin content can be mapped by T2-relaxometry, which resolves multiple differentially relaxing T2 pools from multi-echo MRI. Unfortunately, the conventional fitting procedure is a hard and numerically ill-posed problem. Consequently, the T2 distributions and myelin maps become very sens...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4045663/ https://www.ncbi.nlm.nih.gov/pubmed/24896833 http://dx.doi.org/10.1371/journal.pone.0098391 |
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author | Raj, Ashish Pandya, Sneha Shen, Xiaobo LoCastro, Eve Nguyen, Thanh D. Gauthier, Susan A. |
author_facet | Raj, Ashish Pandya, Sneha Shen, Xiaobo LoCastro, Eve Nguyen, Thanh D. Gauthier, Susan A. |
author_sort | Raj, Ashish |
collection | PubMed |
description | The brain’s myelin content can be mapped by T2-relaxometry, which resolves multiple differentially relaxing T2 pools from multi-echo MRI. Unfortunately, the conventional fitting procedure is a hard and numerically ill-posed problem. Consequently, the T2 distributions and myelin maps become very sensitive to noise and are frequently difficult to interpret diagnostically. Although regularization can improve stability, it is generally not adequate, particularly at relatively low signal to noise ratio (SNR) of around 100–200. The purpose of this study was to obtain a fitting algorithm which is able to overcome these difficulties and generate usable myelin maps from noisy acquisitions in a realistic scan time. To this end, we restrict the T2 distribution to only 3 distinct resolvable tissue compartments, modeled as Gaussians: myelin water, intra/extra-cellular water and a slow relaxing cerebrospinal fluid compartment. We also impose spatial smoothness expectation that volume fractions and T2 relaxation times of tissue compartments change smoothly within coherent brain regions. The method greatly improves robustness to noise, reduces spatial variations, improves definition of white matter fibers, and enhances detection of demyelinating lesions. Due to efficient design, the additional spatial aspect does not cause an increase in processing time. The proposed method was applied to fast spiral acquisitions on which conventional fitting gives uninterpretable results. While these fast acquisitions suffer from noise and inhomogeneity artifacts, our preliminary results indicate the potential of spatially constrained 3-pool T2 relaxometry. |
format | Online Article Text |
id | pubmed-4045663 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-40456632014-06-09 Multi-Compartment T2 Relaxometry Using a Spatially Constrained Multi-Gaussian Model Raj, Ashish Pandya, Sneha Shen, Xiaobo LoCastro, Eve Nguyen, Thanh D. Gauthier, Susan A. PLoS One Research Article The brain’s myelin content can be mapped by T2-relaxometry, which resolves multiple differentially relaxing T2 pools from multi-echo MRI. Unfortunately, the conventional fitting procedure is a hard and numerically ill-posed problem. Consequently, the T2 distributions and myelin maps become very sensitive to noise and are frequently difficult to interpret diagnostically. Although regularization can improve stability, it is generally not adequate, particularly at relatively low signal to noise ratio (SNR) of around 100–200. The purpose of this study was to obtain a fitting algorithm which is able to overcome these difficulties and generate usable myelin maps from noisy acquisitions in a realistic scan time. To this end, we restrict the T2 distribution to only 3 distinct resolvable tissue compartments, modeled as Gaussians: myelin water, intra/extra-cellular water and a slow relaxing cerebrospinal fluid compartment. We also impose spatial smoothness expectation that volume fractions and T2 relaxation times of tissue compartments change smoothly within coherent brain regions. The method greatly improves robustness to noise, reduces spatial variations, improves definition of white matter fibers, and enhances detection of demyelinating lesions. Due to efficient design, the additional spatial aspect does not cause an increase in processing time. The proposed method was applied to fast spiral acquisitions on which conventional fitting gives uninterpretable results. While these fast acquisitions suffer from noise and inhomogeneity artifacts, our preliminary results indicate the potential of spatially constrained 3-pool T2 relaxometry. Public Library of Science 2014-06-04 /pmc/articles/PMC4045663/ /pubmed/24896833 http://dx.doi.org/10.1371/journal.pone.0098391 Text en © 2014 Raj et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Raj, Ashish Pandya, Sneha Shen, Xiaobo LoCastro, Eve Nguyen, Thanh D. Gauthier, Susan A. Multi-Compartment T2 Relaxometry Using a Spatially Constrained Multi-Gaussian Model |
title | Multi-Compartment T2 Relaxometry Using a Spatially Constrained Multi-Gaussian Model |
title_full | Multi-Compartment T2 Relaxometry Using a Spatially Constrained Multi-Gaussian Model |
title_fullStr | Multi-Compartment T2 Relaxometry Using a Spatially Constrained Multi-Gaussian Model |
title_full_unstemmed | Multi-Compartment T2 Relaxometry Using a Spatially Constrained Multi-Gaussian Model |
title_short | Multi-Compartment T2 Relaxometry Using a Spatially Constrained Multi-Gaussian Model |
title_sort | multi-compartment t2 relaxometry using a spatially constrained multi-gaussian model |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4045663/ https://www.ncbi.nlm.nih.gov/pubmed/24896833 http://dx.doi.org/10.1371/journal.pone.0098391 |
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