Cargando…

Quantitative Magnetic Resonance Imaging of Cortical Multiple Sclerosis Pathology

Although significant improvements have been made regarding the visualization and characterization of cortical multiple sclerosis (MS) lesions using magnetic resonance imaging (MRI), cortical lesions (CL) continue to be under-detected in vivo, and we have a limited understanding of the causes of GM p...

Descripción completa

Detalles Bibliográficos
Autores principales: Tardif, Christine L., Bedell, Barry J., Eskildsen, Simon F., Collins, D. Louis, Pike, G. Bruce
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3506905/
https://www.ncbi.nlm.nih.gov/pubmed/23213531
http://dx.doi.org/10.1155/2012/742018
_version_ 1782250976691879936
author Tardif, Christine L.
Bedell, Barry J.
Eskildsen, Simon F.
Collins, D. Louis
Pike, G. Bruce
author_facet Tardif, Christine L.
Bedell, Barry J.
Eskildsen, Simon F.
Collins, D. Louis
Pike, G. Bruce
author_sort Tardif, Christine L.
collection PubMed
description Although significant improvements have been made regarding the visualization and characterization of cortical multiple sclerosis (MS) lesions using magnetic resonance imaging (MRI), cortical lesions (CL) continue to be under-detected in vivo, and we have a limited understanding of the causes of GM pathology. The objective of this study was to characterize the MRI signature of CLs to help interpret the changes seen in vivo and elucidate the factors limiting their visualization. A quantitative 3D high-resolution (350 μm isotropic) MRI study at 3 Tesla of a fixed post mortem cerebral hemisphere from a patient with MS is presented in combination with matched immunohistochemistry. Type III subpial lesions are characterized by an increase in T1, T2 and M0, and a decrease in MTR in comparison to the normal appearing cortex (NAC). All quantitative MR parameters were associated with cortical GM myelin content, while T1 showed the strongest correlation. The histogram analysis showed extensive overlap between CL and NAC for all MR parameters and myelin content. This is due to the poor contrast in myelin content between CL and NAC in comparison to the variability in myelo-architecture throughout the healthy cortex. This latter comparison is highlighted by the representation of T1 times on cortical surfaces at several laminar depths.
format Online
Article
Text
id pubmed-3506905
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Hindawi Publishing Corporation
record_format MEDLINE/PubMed
spelling pubmed-35069052012-12-04 Quantitative Magnetic Resonance Imaging of Cortical Multiple Sclerosis Pathology Tardif, Christine L. Bedell, Barry J. Eskildsen, Simon F. Collins, D. Louis Pike, G. Bruce Mult Scler Int Research Article Although significant improvements have been made regarding the visualization and characterization of cortical multiple sclerosis (MS) lesions using magnetic resonance imaging (MRI), cortical lesions (CL) continue to be under-detected in vivo, and we have a limited understanding of the causes of GM pathology. The objective of this study was to characterize the MRI signature of CLs to help interpret the changes seen in vivo and elucidate the factors limiting their visualization. A quantitative 3D high-resolution (350 μm isotropic) MRI study at 3 Tesla of a fixed post mortem cerebral hemisphere from a patient with MS is presented in combination with matched immunohistochemistry. Type III subpial lesions are characterized by an increase in T1, T2 and M0, and a decrease in MTR in comparison to the normal appearing cortex (NAC). All quantitative MR parameters were associated with cortical GM myelin content, while T1 showed the strongest correlation. The histogram analysis showed extensive overlap between CL and NAC for all MR parameters and myelin content. This is due to the poor contrast in myelin content between CL and NAC in comparison to the variability in myelo-architecture throughout the healthy cortex. This latter comparison is highlighted by the representation of T1 times on cortical surfaces at several laminar depths. Hindawi Publishing Corporation 2012 2012-11-18 /pmc/articles/PMC3506905/ /pubmed/23213531 http://dx.doi.org/10.1155/2012/742018 Text en Copyright © 2012 Christine L. Tardif et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Tardif, Christine L.
Bedell, Barry J.
Eskildsen, Simon F.
Collins, D. Louis
Pike, G. Bruce
Quantitative Magnetic Resonance Imaging of Cortical Multiple Sclerosis Pathology
title Quantitative Magnetic Resonance Imaging of Cortical Multiple Sclerosis Pathology
title_full Quantitative Magnetic Resonance Imaging of Cortical Multiple Sclerosis Pathology
title_fullStr Quantitative Magnetic Resonance Imaging of Cortical Multiple Sclerosis Pathology
title_full_unstemmed Quantitative Magnetic Resonance Imaging of Cortical Multiple Sclerosis Pathology
title_short Quantitative Magnetic Resonance Imaging of Cortical Multiple Sclerosis Pathology
title_sort quantitative magnetic resonance imaging of cortical multiple sclerosis pathology
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3506905/
https://www.ncbi.nlm.nih.gov/pubmed/23213531
http://dx.doi.org/10.1155/2012/742018
work_keys_str_mv AT tardifchristinel quantitativemagneticresonanceimagingofcorticalmultiplesclerosispathology
AT bedellbarryj quantitativemagneticresonanceimagingofcorticalmultiplesclerosispathology
AT eskildsensimonf quantitativemagneticresonanceimagingofcorticalmultiplesclerosispathology
AT collinsdlouis quantitativemagneticresonanceimagingofcorticalmultiplesclerosispathology
AT pikegbruce quantitativemagneticresonanceimagingofcorticalmultiplesclerosispathology