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Whole brain myelin mapping using T1- and T2-weighted MR imaging data
Despite recent advancements in MR imaging, non-invasive mapping of myelin in the brain still remains an open issue. Here we attempted to provide a potential solution. Specifically, we developed a processing workflow based on T1-w and T2-w MR data to generate an optimized myelin enhanced contrast ima...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4151508/ https://www.ncbi.nlm.nih.gov/pubmed/25228871 http://dx.doi.org/10.3389/fnhum.2014.00671 |
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author | Ganzetti, Marco Wenderoth, Nicole Mantini, Dante |
author_facet | Ganzetti, Marco Wenderoth, Nicole Mantini, Dante |
author_sort | Ganzetti, Marco |
collection | PubMed |
description | Despite recent advancements in MR imaging, non-invasive mapping of myelin in the brain still remains an open issue. Here we attempted to provide a potential solution. Specifically, we developed a processing workflow based on T1-w and T2-w MR data to generate an optimized myelin enhanced contrast image. The workflow allows whole brain mapping using the T1-w/T2-w technique, which was originally introduced as a non-invasive method for assessing cortical myelin content. The hallmark of our approach is a retrospective calibration algorithm, applied to bias-corrected T1-w and T2-w images, that relies on image intensities outside the brain. This permits standardizing the intensity histogram of the ratio image, thereby allowing for across-subject statistical analyses. Quantitative comparisons of image histograms within and across different datasets confirmed the effectiveness of our normalization procedure. Not only did the calibrated T1-w/T2-w images exhibit a comparable intensity range, but also the shape of the intensity histograms was largely corresponding. We also assessed the reliability and specificity of the ratio image compared to other MR-based techniques, such as magnetization transfer ratio (MTR), fractional anisotropy (FA), and fluid-attenuated inversion recovery (FLAIR). With respect to these other techniques, T1-w/T2-w had consistently high values, as well as low inter-subject variability, in brain structures where myelin is most abundant. Overall, our results suggested that the T1-w/T2-w technique may be a valid tool supporting the non-invasive mapping of myelin in the brain. Therefore, it might find important applications in the study of brain development, aging and disease. |
format | Online Article Text |
id | pubmed-4151508 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-41515082014-09-16 Whole brain myelin mapping using T1- and T2-weighted MR imaging data Ganzetti, Marco Wenderoth, Nicole Mantini, Dante Front Hum Neurosci Neuroscience Despite recent advancements in MR imaging, non-invasive mapping of myelin in the brain still remains an open issue. Here we attempted to provide a potential solution. Specifically, we developed a processing workflow based on T1-w and T2-w MR data to generate an optimized myelin enhanced contrast image. The workflow allows whole brain mapping using the T1-w/T2-w technique, which was originally introduced as a non-invasive method for assessing cortical myelin content. The hallmark of our approach is a retrospective calibration algorithm, applied to bias-corrected T1-w and T2-w images, that relies on image intensities outside the brain. This permits standardizing the intensity histogram of the ratio image, thereby allowing for across-subject statistical analyses. Quantitative comparisons of image histograms within and across different datasets confirmed the effectiveness of our normalization procedure. Not only did the calibrated T1-w/T2-w images exhibit a comparable intensity range, but also the shape of the intensity histograms was largely corresponding. We also assessed the reliability and specificity of the ratio image compared to other MR-based techniques, such as magnetization transfer ratio (MTR), fractional anisotropy (FA), and fluid-attenuated inversion recovery (FLAIR). With respect to these other techniques, T1-w/T2-w had consistently high values, as well as low inter-subject variability, in brain structures where myelin is most abundant. Overall, our results suggested that the T1-w/T2-w technique may be a valid tool supporting the non-invasive mapping of myelin in the brain. Therefore, it might find important applications in the study of brain development, aging and disease. Frontiers Media S.A. 2014-09-02 /pmc/articles/PMC4151508/ /pubmed/25228871 http://dx.doi.org/10.3389/fnhum.2014.00671 Text en Copyright © 2014 Ganzetti, Wenderoth and Mantini. http://creativecommons.org/licenses/by/3.0/ 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 Ganzetti, Marco Wenderoth, Nicole Mantini, Dante Whole brain myelin mapping using T1- and T2-weighted MR imaging data |
title | Whole brain myelin mapping using T1- and T2-weighted MR imaging data |
title_full | Whole brain myelin mapping using T1- and T2-weighted MR imaging data |
title_fullStr | Whole brain myelin mapping using T1- and T2-weighted MR imaging data |
title_full_unstemmed | Whole brain myelin mapping using T1- and T2-weighted MR imaging data |
title_short | Whole brain myelin mapping using T1- and T2-weighted MR imaging data |
title_sort | whole brain myelin mapping using t1- and t2-weighted mr imaging data |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4151508/ https://www.ncbi.nlm.nih.gov/pubmed/25228871 http://dx.doi.org/10.3389/fnhum.2014.00671 |
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