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Diffusion magnetic resonance imaging of normal-appearing white matter in multiple sclerosis: correlation with brain volume and clinical disability

BACKGROUND: Diffusion magnetic resonance imaging (MRI) abnormalities in multiple sclerosis (MS) are not limited to lesions, but have also been observed in the white matter that appears normal on conventional MRI sequences, known as normal-appearing white matter (NAWM). There is evidence of microstru...

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Autores principales: Larassati, Hana, Pandelaki, Jacub, Estiasari, Riwanti, Prihartono, Joedo, Firdausia, Salsabila, Yunus, Reyhan Eddy, Mulyadi, Rahmad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9092575/
https://www.ncbi.nlm.nih.gov/pubmed/35572123
http://dx.doi.org/10.1177/11795735221098147
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author Larassati, Hana
Pandelaki, Jacub
Estiasari, Riwanti
Prihartono, Joedo
Firdausia, Salsabila
Yunus, Reyhan Eddy
Mulyadi, Rahmad
author_facet Larassati, Hana
Pandelaki, Jacub
Estiasari, Riwanti
Prihartono, Joedo
Firdausia, Salsabila
Yunus, Reyhan Eddy
Mulyadi, Rahmad
author_sort Larassati, Hana
collection PubMed
description BACKGROUND: Diffusion magnetic resonance imaging (MRI) abnormalities in multiple sclerosis (MS) are not limited to lesions, but have also been observed in the white matter that appears normal on conventional MRI sequences, known as normal-appearing white matter (NAWM). There is evidence of microstructural processes occurring in the NAWM. OBJECTIVE: To assess the correlation between NAWM apparent diffusion coefficient (ADC) and fractional anisotropy (FA) with brain volume and clinical disability in MS. METHODS: Brain MRI from 33 MS patients were included. ADC and FA measurements of the genu, body, and splenium of corpus callosum (CC) were done. ADC and FA values were analyzed to measure their correlation with brain volume from MR volumetry and clinical disability represented by Expanded Disability Status Scale (EDSS). RESULTS: The mean ADC of CC NAWM was .93 ×10(−3) mm(2)/s (±.13 SD), and the mean FA .72 (±.12 SD). ADC and FA of CC NAWM were significantly correlated with the ratio of brain volume to intracranial volume (R = −0,70 and 0,78 respectively), and with EDSS (R = .52 and −.59 respectively). CONCLUSION: There were significant correlations between ADC and FA of NAWM with brain volume and EDSS of MS patients. Further longitudinal studies were needed to evaluate the potential of diffusion MRI in the evaluation of MS.
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spelling pubmed-90925752022-05-12 Diffusion magnetic resonance imaging of normal-appearing white matter in multiple sclerosis: correlation with brain volume and clinical disability Larassati, Hana Pandelaki, Jacub Estiasari, Riwanti Prihartono, Joedo Firdausia, Salsabila Yunus, Reyhan Eddy Mulyadi, Rahmad J Cent Nerv Syst Dis Original Research Article BACKGROUND: Diffusion magnetic resonance imaging (MRI) abnormalities in multiple sclerosis (MS) are not limited to lesions, but have also been observed in the white matter that appears normal on conventional MRI sequences, known as normal-appearing white matter (NAWM). There is evidence of microstructural processes occurring in the NAWM. OBJECTIVE: To assess the correlation between NAWM apparent diffusion coefficient (ADC) and fractional anisotropy (FA) with brain volume and clinical disability in MS. METHODS: Brain MRI from 33 MS patients were included. ADC and FA measurements of the genu, body, and splenium of corpus callosum (CC) were done. ADC and FA values were analyzed to measure their correlation with brain volume from MR volumetry and clinical disability represented by Expanded Disability Status Scale (EDSS). RESULTS: The mean ADC of CC NAWM was .93 ×10(−3) mm(2)/s (±.13 SD), and the mean FA .72 (±.12 SD). ADC and FA of CC NAWM were significantly correlated with the ratio of brain volume to intracranial volume (R = −0,70 and 0,78 respectively), and with EDSS (R = .52 and −.59 respectively). CONCLUSION: There were significant correlations between ADC and FA of NAWM with brain volume and EDSS of MS patients. Further longitudinal studies were needed to evaluate the potential of diffusion MRI in the evaluation of MS. SAGE Publications 2022-05-08 /pmc/articles/PMC9092575/ /pubmed/35572123 http://dx.doi.org/10.1177/11795735221098147 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research Article
Larassati, Hana
Pandelaki, Jacub
Estiasari, Riwanti
Prihartono, Joedo
Firdausia, Salsabila
Yunus, Reyhan Eddy
Mulyadi, Rahmad
Diffusion magnetic resonance imaging of normal-appearing white matter in multiple sclerosis: correlation with brain volume and clinical disability
title Diffusion magnetic resonance imaging of normal-appearing white matter in multiple sclerosis: correlation with brain volume and clinical disability
title_full Diffusion magnetic resonance imaging of normal-appearing white matter in multiple sclerosis: correlation with brain volume and clinical disability
title_fullStr Diffusion magnetic resonance imaging of normal-appearing white matter in multiple sclerosis: correlation with brain volume and clinical disability
title_full_unstemmed Diffusion magnetic resonance imaging of normal-appearing white matter in multiple sclerosis: correlation with brain volume and clinical disability
title_short Diffusion magnetic resonance imaging of normal-appearing white matter in multiple sclerosis: correlation with brain volume and clinical disability
title_sort diffusion magnetic resonance imaging of normal-appearing white matter in multiple sclerosis: correlation with brain volume and clinical disability
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9092575/
https://www.ncbi.nlm.nih.gov/pubmed/35572123
http://dx.doi.org/10.1177/11795735221098147
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