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Assessing intracortical myelin in the living human brain using myelinated cortical thickness
Alterations in the myelination of the cerebral cortex may underlie abnormal cortical function in a variety of brain diseases. Here, we describe a technique for investigating changes in intracortical myelin in clinical populations on the basis of cortical thickness measurements with magnetic resonanc...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4615825/ https://www.ncbi.nlm.nih.gov/pubmed/26557052 http://dx.doi.org/10.3389/fnins.2015.00396 |
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author | Rowley, Christopher D. Bazin, Pierre-Louis Tardif, Christine L. Sehmbi, Manpreet Hashim, Eyesha Zaharieva, Nadejda Minuzzi, Luciano Frey, Benicio N. Bock, Nicholas A. |
author_facet | Rowley, Christopher D. Bazin, Pierre-Louis Tardif, Christine L. Sehmbi, Manpreet Hashim, Eyesha Zaharieva, Nadejda Minuzzi, Luciano Frey, Benicio N. Bock, Nicholas A. |
author_sort | Rowley, Christopher D. |
collection | PubMed |
description | Alterations in the myelination of the cerebral cortex may underlie abnormal cortical function in a variety of brain diseases. Here, we describe a technique for investigating changes in intracortical myelin in clinical populations on the basis of cortical thickness measurements with magnetic resonance imaging (MRI) at 3 Tesla. For this, we separately compute the thickness of the shallower, lightly myelinated portion of the cortex and its deeper, heavily myelinated portion (referred to herein as unmyelinated and myelinated cortex, respectively). Our expectation is that the thickness of the myelinated cortex will be a specific biomarker for disruptions in myeloarchitecture. We show representative atlases of total cortical thickness, T, unmyelinated cortical thickness, G, and myelinated cortical thickness, M, for a healthy group of 20 female subjects. We further demonstrate myelinated cortical thickness measurements in a preliminary clinical study of 10 bipolar disorder type-I subjects and 10 healthy controls, and report significant decreases in the middle frontal gyrus in T, G, and M in the disorder, with the largest percentage change occurring in M. This study highlights the potential of myelinated cortical thickness measurements for investigating intracortical myelin involvement in brain disease at clinically relevant field strengths and resolutions. |
format | Online Article Text |
id | pubmed-4615825 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-46158252015-11-09 Assessing intracortical myelin in the living human brain using myelinated cortical thickness Rowley, Christopher D. Bazin, Pierre-Louis Tardif, Christine L. Sehmbi, Manpreet Hashim, Eyesha Zaharieva, Nadejda Minuzzi, Luciano Frey, Benicio N. Bock, Nicholas A. Front Neurosci Neuroscience Alterations in the myelination of the cerebral cortex may underlie abnormal cortical function in a variety of brain diseases. Here, we describe a technique for investigating changes in intracortical myelin in clinical populations on the basis of cortical thickness measurements with magnetic resonance imaging (MRI) at 3 Tesla. For this, we separately compute the thickness of the shallower, lightly myelinated portion of the cortex and its deeper, heavily myelinated portion (referred to herein as unmyelinated and myelinated cortex, respectively). Our expectation is that the thickness of the myelinated cortex will be a specific biomarker for disruptions in myeloarchitecture. We show representative atlases of total cortical thickness, T, unmyelinated cortical thickness, G, and myelinated cortical thickness, M, for a healthy group of 20 female subjects. We further demonstrate myelinated cortical thickness measurements in a preliminary clinical study of 10 bipolar disorder type-I subjects and 10 healthy controls, and report significant decreases in the middle frontal gyrus in T, G, and M in the disorder, with the largest percentage change occurring in M. This study highlights the potential of myelinated cortical thickness measurements for investigating intracortical myelin involvement in brain disease at clinically relevant field strengths and resolutions. Frontiers Media S.A. 2015-10-23 /pmc/articles/PMC4615825/ /pubmed/26557052 http://dx.doi.org/10.3389/fnins.2015.00396 Text en Copyright © 2015 Rowley, Bazin, Tardif, Sehmbi, Hashim, Zaharieva, Minuzzi, Frey and Bock. 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) or licensor 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 Rowley, Christopher D. Bazin, Pierre-Louis Tardif, Christine L. Sehmbi, Manpreet Hashim, Eyesha Zaharieva, Nadejda Minuzzi, Luciano Frey, Benicio N. Bock, Nicholas A. Assessing intracortical myelin in the living human brain using myelinated cortical thickness |
title | Assessing intracortical myelin in the living human brain using myelinated cortical thickness |
title_full | Assessing intracortical myelin in the living human brain using myelinated cortical thickness |
title_fullStr | Assessing intracortical myelin in the living human brain using myelinated cortical thickness |
title_full_unstemmed | Assessing intracortical myelin in the living human brain using myelinated cortical thickness |
title_short | Assessing intracortical myelin in the living human brain using myelinated cortical thickness |
title_sort | assessing intracortical myelin in the living human brain using myelinated cortical thickness |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4615825/ https://www.ncbi.nlm.nih.gov/pubmed/26557052 http://dx.doi.org/10.3389/fnins.2015.00396 |
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