Cargando…

Reproducibility and Reliability of Quantitative and Weighted T(1) and T(2)(∗) Mapping for Myelin-Based Cortical Parcellation at 7 Tesla

Different magnetic resonance (MR) parameters, such as R(1) (=1/T(1)) or T(2)(∗), have been used to visualize non-invasively the myelin distribution across the cortical sheet. Myelin contrast is consistently enhanced in the primary sensory and some higher order cortical areas (such as MT or the cingu...

Descripción completa

Detalles Bibliográficos
Autores principales: Haast, Roy A. M., Ivanov, Dimo, Formisano, Elia, Uludaǧ, Kâmil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5114304/
https://www.ncbi.nlm.nih.gov/pubmed/27917112
http://dx.doi.org/10.3389/fnana.2016.00112
_version_ 1782468324631773184
author Haast, Roy A. M.
Ivanov, Dimo
Formisano, Elia
Uludaǧ, Kâmil
author_facet Haast, Roy A. M.
Ivanov, Dimo
Formisano, Elia
Uludaǧ, Kâmil
author_sort Haast, Roy A. M.
collection PubMed
description Different magnetic resonance (MR) parameters, such as R(1) (=1/T(1)) or T(2)(∗), have been used to visualize non-invasively the myelin distribution across the cortical sheet. Myelin contrast is consistently enhanced in the primary sensory and some higher order cortical areas (such as MT or the cingulate cortex), which renders it suitable for subject-specific anatomical cortical parcellation. However, no systematic comparison has been performed between the previously proposed MR parameters, i.e., the longitudinal and transversal relaxation values (or their ratios), for myelin mapping at 7 Tesla. In addition, usually these MR parameters are acquired in a non-quantitative manner (“weighted” parameters). Here, we evaluated the differences in ‘parcellability,’ contrast-to-noise ratio (CNR) and inter- and intra-subject variability and reproducibility, respectively, between high-resolution cortical surface maps based on these weighted MR parameters and their quantitative counterparts in ten healthy subjects. All parameters were obtained in a similar acquisition time and possible transmit- or receive-biases were removed during post-processing. It was found that CNR per unit time and parcellability were lower for the transversal compared to the longitudinal relaxation parameters. Further, quantitative R(1) was characterized by the lowest inter- and intra-subject coefficient of variation (5.53 and 1.63%, respectively), making R(1) a better parameter to map the myelin distribution compared to the other parameters. Moreover, quantitative MRI approaches offer the advantage of absolute rather than relative characterization of the underlying biochemical composition of the tissue, allowing more reliable comparison within subjects and between healthy subjects and patients. Finally, we explored two parcellation methods (thresholding the MR parameter values vs. surface gradients of these values) to determine areal borders based on the cortical surface pattern. It is shown that both methods are partially observer-dependent, needing manual interaction (i.e., choice of threshold or connecting high gradient values) to provide unambiguous borders.
format Online
Article
Text
id pubmed-5114304
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-51143042016-12-02 Reproducibility and Reliability of Quantitative and Weighted T(1) and T(2)(∗) Mapping for Myelin-Based Cortical Parcellation at 7 Tesla Haast, Roy A. M. Ivanov, Dimo Formisano, Elia Uludaǧ, Kâmil Front Neuroanat Neuroanatomy Different magnetic resonance (MR) parameters, such as R(1) (=1/T(1)) or T(2)(∗), have been used to visualize non-invasively the myelin distribution across the cortical sheet. Myelin contrast is consistently enhanced in the primary sensory and some higher order cortical areas (such as MT or the cingulate cortex), which renders it suitable for subject-specific anatomical cortical parcellation. However, no systematic comparison has been performed between the previously proposed MR parameters, i.e., the longitudinal and transversal relaxation values (or their ratios), for myelin mapping at 7 Tesla. In addition, usually these MR parameters are acquired in a non-quantitative manner (“weighted” parameters). Here, we evaluated the differences in ‘parcellability,’ contrast-to-noise ratio (CNR) and inter- and intra-subject variability and reproducibility, respectively, between high-resolution cortical surface maps based on these weighted MR parameters and their quantitative counterparts in ten healthy subjects. All parameters were obtained in a similar acquisition time and possible transmit- or receive-biases were removed during post-processing. It was found that CNR per unit time and parcellability were lower for the transversal compared to the longitudinal relaxation parameters. Further, quantitative R(1) was characterized by the lowest inter- and intra-subject coefficient of variation (5.53 and 1.63%, respectively), making R(1) a better parameter to map the myelin distribution compared to the other parameters. Moreover, quantitative MRI approaches offer the advantage of absolute rather than relative characterization of the underlying biochemical composition of the tissue, allowing more reliable comparison within subjects and between healthy subjects and patients. Finally, we explored two parcellation methods (thresholding the MR parameter values vs. surface gradients of these values) to determine areal borders based on the cortical surface pattern. It is shown that both methods are partially observer-dependent, needing manual interaction (i.e., choice of threshold or connecting high gradient values) to provide unambiguous borders. Frontiers Media S.A. 2016-11-18 /pmc/articles/PMC5114304/ /pubmed/27917112 http://dx.doi.org/10.3389/fnana.2016.00112 Text en Copyright © 2016 Haast, Ivanov, Formisano and Uludaǧ. 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 Neuroanatomy
Haast, Roy A. M.
Ivanov, Dimo
Formisano, Elia
Uludaǧ, Kâmil
Reproducibility and Reliability of Quantitative and Weighted T(1) and T(2)(∗) Mapping for Myelin-Based Cortical Parcellation at 7 Tesla
title Reproducibility and Reliability of Quantitative and Weighted T(1) and T(2)(∗) Mapping for Myelin-Based Cortical Parcellation at 7 Tesla
title_full Reproducibility and Reliability of Quantitative and Weighted T(1) and T(2)(∗) Mapping for Myelin-Based Cortical Parcellation at 7 Tesla
title_fullStr Reproducibility and Reliability of Quantitative and Weighted T(1) and T(2)(∗) Mapping for Myelin-Based Cortical Parcellation at 7 Tesla
title_full_unstemmed Reproducibility and Reliability of Quantitative and Weighted T(1) and T(2)(∗) Mapping for Myelin-Based Cortical Parcellation at 7 Tesla
title_short Reproducibility and Reliability of Quantitative and Weighted T(1) and T(2)(∗) Mapping for Myelin-Based Cortical Parcellation at 7 Tesla
title_sort reproducibility and reliability of quantitative and weighted t(1) and t(2)(∗) mapping for myelin-based cortical parcellation at 7 tesla
topic Neuroanatomy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5114304/
https://www.ncbi.nlm.nih.gov/pubmed/27917112
http://dx.doi.org/10.3389/fnana.2016.00112
work_keys_str_mv AT haastroyam reproducibilityandreliabilityofquantitativeandweightedt1andt2mappingformyelinbasedcorticalparcellationat7tesla
AT ivanovdimo reproducibilityandreliabilityofquantitativeandweightedt1andt2mappingformyelinbasedcorticalparcellationat7tesla
AT formisanoelia reproducibilityandreliabilityofquantitativeandweightedt1andt2mappingformyelinbasedcorticalparcellationat7tesla
AT uludagkamil reproducibilityandreliabilityofquantitativeandweightedt1andt2mappingformyelinbasedcorticalparcellationat7tesla