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Permanent tissue damage in multiple sclerosis lesions is associated with reduced pre-lesion myelin and axon volume fractions

BACKGROUND: The use of advanced magnetic resonance imaging (MRI) techniques in MS research has led to new insights in lesion evolution and disease outcomes. It has not yet been determined if, or how, pre-lesional abnormalities in normal-appearing white matter (NAWM) relate to the long-term evolution...

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Autores principales: Tagge, Ian J, Leppert, Ilana R, Fetco, Dumitru, Campbell, Jennifer SW, Rudko, David A, Brown, Robert A, Stikov, Nikola, Pike, G Bruce, Giacomini, Paul S, Arnold, Douglas L, Narayanan, Sridar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9574230/
https://www.ncbi.nlm.nih.gov/pubmed/35903888
http://dx.doi.org/10.1177/13524585221110585
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author Tagge, Ian J
Leppert, Ilana R
Fetco, Dumitru
Campbell, Jennifer SW
Rudko, David A
Brown, Robert A
Stikov, Nikola
Pike, G Bruce
Giacomini, Paul S
Arnold, Douglas L
Narayanan, Sridar
author_facet Tagge, Ian J
Leppert, Ilana R
Fetco, Dumitru
Campbell, Jennifer SW
Rudko, David A
Brown, Robert A
Stikov, Nikola
Pike, G Bruce
Giacomini, Paul S
Arnold, Douglas L
Narayanan, Sridar
author_sort Tagge, Ian J
collection PubMed
description BACKGROUND: The use of advanced magnetic resonance imaging (MRI) techniques in MS research has led to new insights in lesion evolution and disease outcomes. It has not yet been determined if, or how, pre-lesional abnormalities in normal-appearing white matter (NAWM) relate to the long-term evolution of new lesions. OBJECTIVE: To investigate the relationship between abnormalities in MRI measures of axonal and myelin volume fractions (AVF and MVF) in NAWM preceding development of black-hole (BH) and non-BH lesions in people with MS. METHODS: We obtained magnetization transfer and diffusion MRI at 6-month intervals in patients with MS to estimate MVF and AVF during lesion evolution. Lesions were classified as either BH or non-BH on the final imaging visit using T(1) maps. RESULTS: Longitudinal data from 97 new T(2) lesions from 9 participants were analyzed; 25 lesions in 8 participants were classified as BH 6–12 months after initial appearance. Pre-lesion MVF, AVF, and MVF/AVF were significantly lower, and T(1) was significantly higher, in the lesions that later became BHs (p < 0.001) compared to those that did not. No significant pre-lesion abnormalities were found in non-BH lesions (p > 0.05). CONCLUSION: The present work demonstrated that pre-lesion abnormalities are associated with worse long-term lesion-level outcome.
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spelling pubmed-95742302022-10-18 Permanent tissue damage in multiple sclerosis lesions is associated with reduced pre-lesion myelin and axon volume fractions Tagge, Ian J Leppert, Ilana R Fetco, Dumitru Campbell, Jennifer SW Rudko, David A Brown, Robert A Stikov, Nikola Pike, G Bruce Giacomini, Paul S Arnold, Douglas L Narayanan, Sridar Mult Scler Original Research Papers BACKGROUND: The use of advanced magnetic resonance imaging (MRI) techniques in MS research has led to new insights in lesion evolution and disease outcomes. It has not yet been determined if, or how, pre-lesional abnormalities in normal-appearing white matter (NAWM) relate to the long-term evolution of new lesions. OBJECTIVE: To investigate the relationship between abnormalities in MRI measures of axonal and myelin volume fractions (AVF and MVF) in NAWM preceding development of black-hole (BH) and non-BH lesions in people with MS. METHODS: We obtained magnetization transfer and diffusion MRI at 6-month intervals in patients with MS to estimate MVF and AVF during lesion evolution. Lesions were classified as either BH or non-BH on the final imaging visit using T(1) maps. RESULTS: Longitudinal data from 97 new T(2) lesions from 9 participants were analyzed; 25 lesions in 8 participants were classified as BH 6–12 months after initial appearance. Pre-lesion MVF, AVF, and MVF/AVF were significantly lower, and T(1) was significantly higher, in the lesions that later became BHs (p < 0.001) compared to those that did not. No significant pre-lesion abnormalities were found in non-BH lesions (p > 0.05). CONCLUSION: The present work demonstrated that pre-lesion abnormalities are associated with worse long-term lesion-level outcome. SAGE Publications 2022-07-28 2022-11 /pmc/articles/PMC9574230/ /pubmed/35903888 http://dx.doi.org/10.1177/13524585221110585 Text en © The Author(s), 2022 https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research Papers
Tagge, Ian J
Leppert, Ilana R
Fetco, Dumitru
Campbell, Jennifer SW
Rudko, David A
Brown, Robert A
Stikov, Nikola
Pike, G Bruce
Giacomini, Paul S
Arnold, Douglas L
Narayanan, Sridar
Permanent tissue damage in multiple sclerosis lesions is associated with reduced pre-lesion myelin and axon volume fractions
title Permanent tissue damage in multiple sclerosis lesions is associated with reduced pre-lesion myelin and axon volume fractions
title_full Permanent tissue damage in multiple sclerosis lesions is associated with reduced pre-lesion myelin and axon volume fractions
title_fullStr Permanent tissue damage in multiple sclerosis lesions is associated with reduced pre-lesion myelin and axon volume fractions
title_full_unstemmed Permanent tissue damage in multiple sclerosis lesions is associated with reduced pre-lesion myelin and axon volume fractions
title_short Permanent tissue damage in multiple sclerosis lesions is associated with reduced pre-lesion myelin and axon volume fractions
title_sort permanent tissue damage in multiple sclerosis lesions is associated with reduced pre-lesion myelin and axon volume fractions
topic Original Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9574230/
https://www.ncbi.nlm.nih.gov/pubmed/35903888
http://dx.doi.org/10.1177/13524585221110585
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