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Feasibility of Imaging Myelin Lesions in Multiple Sclerosis

The goal of this study was to provide a feasibility assessment for PET imaging of multiple sclerosis (MS) lesions based on their decreased myelin content relative to the surrounding normal-appearing brain tissue. The imaging agent evaluated for this purpose is a molecule that binds strongly and spec...

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Detalles Bibliográficos
Autores principales: Zavodszky, Maria I., Graf, John F., Tan Hehir, Cristina A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3157216/
https://www.ncbi.nlm.nih.gov/pubmed/21860614
http://dx.doi.org/10.1155/2011/953806
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author Zavodszky, Maria I.
Graf, John F.
Tan Hehir, Cristina A.
author_facet Zavodszky, Maria I.
Graf, John F.
Tan Hehir, Cristina A.
author_sort Zavodszky, Maria I.
collection PubMed
description The goal of this study was to provide a feasibility assessment for PET imaging of multiple sclerosis (MS) lesions based on their decreased myelin content relative to the surrounding normal-appearing brain tissue. The imaging agent evaluated for this purpose is a molecule that binds strongly and specifically to myelin basic protein. Physiology-based pharmacokinetic modeling combined with PET image simulation applied to a brain model was used to examine whether such an agent would allow the differentiation of artificial lesions 4–10 mm in diameter from the surrounding normal-looking white and gray matter. Furthermore, we examined how changes in agent properties, model parameters, and experimental conditions can influence imageability, identifying a set of conditions under which imaging of MS lesions might be feasible. Based on our results, we concluded that PET imaging has the potential to become a useful complementary method to MRI for MS diagnosis and therapy monitoring.
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spelling pubmed-31572162011-08-22 Feasibility of Imaging Myelin Lesions in Multiple Sclerosis Zavodszky, Maria I. Graf, John F. Tan Hehir, Cristina A. Int J Biomed Imaging Research Article The goal of this study was to provide a feasibility assessment for PET imaging of multiple sclerosis (MS) lesions based on their decreased myelin content relative to the surrounding normal-appearing brain tissue. The imaging agent evaluated for this purpose is a molecule that binds strongly and specifically to myelin basic protein. Physiology-based pharmacokinetic modeling combined with PET image simulation applied to a brain model was used to examine whether such an agent would allow the differentiation of artificial lesions 4–10 mm in diameter from the surrounding normal-looking white and gray matter. Furthermore, we examined how changes in agent properties, model parameters, and experimental conditions can influence imageability, identifying a set of conditions under which imaging of MS lesions might be feasible. Based on our results, we concluded that PET imaging has the potential to become a useful complementary method to MRI for MS diagnosis and therapy monitoring. Hindawi Publishing Corporation 2011 2011-08-15 /pmc/articles/PMC3157216/ /pubmed/21860614 http://dx.doi.org/10.1155/2011/953806 Text en Copyright © 2011 Maria I. Zavodszky 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
Zavodszky, Maria I.
Graf, John F.
Tan Hehir, Cristina A.
Feasibility of Imaging Myelin Lesions in Multiple Sclerosis
title Feasibility of Imaging Myelin Lesions in Multiple Sclerosis
title_full Feasibility of Imaging Myelin Lesions in Multiple Sclerosis
title_fullStr Feasibility of Imaging Myelin Lesions in Multiple Sclerosis
title_full_unstemmed Feasibility of Imaging Myelin Lesions in Multiple Sclerosis
title_short Feasibility of Imaging Myelin Lesions in Multiple Sclerosis
title_sort feasibility of imaging myelin lesions in multiple sclerosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3157216/
https://www.ncbi.nlm.nih.gov/pubmed/21860614
http://dx.doi.org/10.1155/2011/953806
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