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Quantitative assessment of myelination patterns in preterm neonates using T2-weighted MRI
Myelination is considered to be an important developmental process during human brain maturation and closely correlated with gestational age. Quantitative assessment of the myelination status requires dedicated imaging, but the conventional T(2)-weighted scans routinely acquired during clinical imag...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6736873/ https://www.ncbi.nlm.nih.gov/pubmed/31506514 http://dx.doi.org/10.1038/s41598-019-49350-3 |
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author | Wang, Siying Ledig, Christian Hajnal, Joseph V. Counsell, Serena J. Schnabel, Julia A. Deprez, Maria |
author_facet | Wang, Siying Ledig, Christian Hajnal, Joseph V. Counsell, Serena J. Schnabel, Julia A. Deprez, Maria |
author_sort | Wang, Siying |
collection | PubMed |
description | Myelination is considered to be an important developmental process during human brain maturation and closely correlated with gestational age. Quantitative assessment of the myelination status requires dedicated imaging, but the conventional T(2)-weighted scans routinely acquired during clinical imaging of neonates carry signatures that are thought to be associated with myelination. In this work, we develop a quatitative marker of progressing myelination for assessment preterm neonatal brain maturation based on novel automatic segmentation method for myelin-like signals on T(2)-weighted magnetic resonance images. Firstly we define a segmentation protocol for myelin-like signals. We then develop an expectation-maximization framework to obtain the automatic segmentations of myelin-like signals with explicit class for partial volume voxels whose locations are configured in relation to the composing pure tissues via second-order Markov random fields. The proposed segmentation achieves high Dice overlaps of 0.83 with manual annotations. The automatic segmentations are then used to track volumes of myelinated tissues in the regions of the central brain structures and brainstem. Finally, we construct a spatio-temporal growth models for myelin-like signals, which allows us to predict gestational age at scan in preterm infants with root mean squared error 1.41 weeks. |
format | Online Article Text |
id | pubmed-6736873 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67368732019-09-20 Quantitative assessment of myelination patterns in preterm neonates using T2-weighted MRI Wang, Siying Ledig, Christian Hajnal, Joseph V. Counsell, Serena J. Schnabel, Julia A. Deprez, Maria Sci Rep Article Myelination is considered to be an important developmental process during human brain maturation and closely correlated with gestational age. Quantitative assessment of the myelination status requires dedicated imaging, but the conventional T(2)-weighted scans routinely acquired during clinical imaging of neonates carry signatures that are thought to be associated with myelination. In this work, we develop a quatitative marker of progressing myelination for assessment preterm neonatal brain maturation based on novel automatic segmentation method for myelin-like signals on T(2)-weighted magnetic resonance images. Firstly we define a segmentation protocol for myelin-like signals. We then develop an expectation-maximization framework to obtain the automatic segmentations of myelin-like signals with explicit class for partial volume voxels whose locations are configured in relation to the composing pure tissues via second-order Markov random fields. The proposed segmentation achieves high Dice overlaps of 0.83 with manual annotations. The automatic segmentations are then used to track volumes of myelinated tissues in the regions of the central brain structures and brainstem. Finally, we construct a spatio-temporal growth models for myelin-like signals, which allows us to predict gestational age at scan in preterm infants with root mean squared error 1.41 weeks. Nature Publishing Group UK 2019-09-10 /pmc/articles/PMC6736873/ /pubmed/31506514 http://dx.doi.org/10.1038/s41598-019-49350-3 Text en © The Author(s) 2019 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Wang, Siying Ledig, Christian Hajnal, Joseph V. Counsell, Serena J. Schnabel, Julia A. Deprez, Maria Quantitative assessment of myelination patterns in preterm neonates using T2-weighted MRI |
title | Quantitative assessment of myelination patterns in preterm neonates using T2-weighted MRI |
title_full | Quantitative assessment of myelination patterns in preterm neonates using T2-weighted MRI |
title_fullStr | Quantitative assessment of myelination patterns in preterm neonates using T2-weighted MRI |
title_full_unstemmed | Quantitative assessment of myelination patterns in preterm neonates using T2-weighted MRI |
title_short | Quantitative assessment of myelination patterns in preterm neonates using T2-weighted MRI |
title_sort | quantitative assessment of myelination patterns in preterm neonates using t2-weighted mri |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6736873/ https://www.ncbi.nlm.nih.gov/pubmed/31506514 http://dx.doi.org/10.1038/s41598-019-49350-3 |
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