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Brain White Matter Hyperintensity Lesion Characterization in T(2) Fluid-Attenuated Inversion Recovery Magnetic Resonance Images: Shape, Texture, and Potential Growth

Prior methods in characterizing age-related white matter hyperintensity (WMH) lesions on T(2) fluid-attenuated inversion recovery (FLAIR) magnetic resonance images (MRI) have mainly been limited to understanding the sizes of, and occasionally the locations of WMH lesions. Systematic morphological ch...

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Autores principales: Gwo, Chih-Ying, Zhu, David C., Zhang, Rong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6477529/
https://www.ncbi.nlm.nih.gov/pubmed/31057353
http://dx.doi.org/10.3389/fnins.2019.00353
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author Gwo, Chih-Ying
Zhu, David C.
Zhang, Rong
author_facet Gwo, Chih-Ying
Zhu, David C.
Zhang, Rong
author_sort Gwo, Chih-Ying
collection PubMed
description Prior methods in characterizing age-related white matter hyperintensity (WMH) lesions on T(2) fluid-attenuated inversion recovery (FLAIR) magnetic resonance images (MRI) have mainly been limited to understanding the sizes of, and occasionally the locations of WMH lesions. Systematic morphological characterization has been missing. In this work, we proposed innovative methods to fill this knowledge gap. We developed an innovative and proof-of-concept method to characterize and quantify the shape (based on Zernike transformation) and texture (based on fuzzy logic) of WMH lesions. We have also developed a multi-dimension feature vector approach to cluster WMH lesions into distinctive groups based on their shape and then texture features. We then developed an approach to calculate the potential growth index (PGI) of WMH lesions based on the image intensity distributions at the edge of the WMH lesions using a region-growing algorithm. High-quality T(2) FLAIR images containing clearly identifiable WMH lesions with various sizes from six cognitively normal older adults were used in our method development Analyses of Variance (ANOVAs) showed significant differences in PGI among WMH group clusters in terms of either the shape (P = 1.06 × 10(−2)) or the texture (P < 1 × 10(−20)) features. In conclusion, we propose a systematic framework on which the shape and texture features of WMH lesions can be quantified and may be used to predict lesion growth in older adults.
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spelling pubmed-64775292019-05-03 Brain White Matter Hyperintensity Lesion Characterization in T(2) Fluid-Attenuated Inversion Recovery Magnetic Resonance Images: Shape, Texture, and Potential Growth Gwo, Chih-Ying Zhu, David C. Zhang, Rong Front Neurosci Neuroscience Prior methods in characterizing age-related white matter hyperintensity (WMH) lesions on T(2) fluid-attenuated inversion recovery (FLAIR) magnetic resonance images (MRI) have mainly been limited to understanding the sizes of, and occasionally the locations of WMH lesions. Systematic morphological characterization has been missing. In this work, we proposed innovative methods to fill this knowledge gap. We developed an innovative and proof-of-concept method to characterize and quantify the shape (based on Zernike transformation) and texture (based on fuzzy logic) of WMH lesions. We have also developed a multi-dimension feature vector approach to cluster WMH lesions into distinctive groups based on their shape and then texture features. We then developed an approach to calculate the potential growth index (PGI) of WMH lesions based on the image intensity distributions at the edge of the WMH lesions using a region-growing algorithm. High-quality T(2) FLAIR images containing clearly identifiable WMH lesions with various sizes from six cognitively normal older adults were used in our method development Analyses of Variance (ANOVAs) showed significant differences in PGI among WMH group clusters in terms of either the shape (P = 1.06 × 10(−2)) or the texture (P < 1 × 10(−20)) features. In conclusion, we propose a systematic framework on which the shape and texture features of WMH lesions can be quantified and may be used to predict lesion growth in older adults. Frontiers Media S.A. 2019-04-16 /pmc/articles/PMC6477529/ /pubmed/31057353 http://dx.doi.org/10.3389/fnins.2019.00353 Text en Copyright © 2019 Gwo, Zhu and Zhang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Gwo, Chih-Ying
Zhu, David C.
Zhang, Rong
Brain White Matter Hyperintensity Lesion Characterization in T(2) Fluid-Attenuated Inversion Recovery Magnetic Resonance Images: Shape, Texture, and Potential Growth
title Brain White Matter Hyperintensity Lesion Characterization in T(2) Fluid-Attenuated Inversion Recovery Magnetic Resonance Images: Shape, Texture, and Potential Growth
title_full Brain White Matter Hyperintensity Lesion Characterization in T(2) Fluid-Attenuated Inversion Recovery Magnetic Resonance Images: Shape, Texture, and Potential Growth
title_fullStr Brain White Matter Hyperintensity Lesion Characterization in T(2) Fluid-Attenuated Inversion Recovery Magnetic Resonance Images: Shape, Texture, and Potential Growth
title_full_unstemmed Brain White Matter Hyperintensity Lesion Characterization in T(2) Fluid-Attenuated Inversion Recovery Magnetic Resonance Images: Shape, Texture, and Potential Growth
title_short Brain White Matter Hyperintensity Lesion Characterization in T(2) Fluid-Attenuated Inversion Recovery Magnetic Resonance Images: Shape, Texture, and Potential Growth
title_sort brain white matter hyperintensity lesion characterization in t(2) fluid-attenuated inversion recovery magnetic resonance images: shape, texture, and potential growth
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6477529/
https://www.ncbi.nlm.nih.gov/pubmed/31057353
http://dx.doi.org/10.3389/fnins.2019.00353
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