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Leptomeningeal Contrast Enhancement Is Associated with Disability Progression and Grey Matter Atrophy in Multiple Sclerosis

Leptomeningeal contrast enhancement (LMCE) on magnetic resonance imaging (MRI) is a newly recognized possible biomarker in multiple sclerosis (MS), associated with MS progression and cortical atrophy. In this study, we aimed to assess the prevalence of LMCE foci and their impact on neurodegeneration...

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Autores principales: Makshakov, Gleb, Magonov, Evgeniy, Totolyan, Natalia, Nazarov, Vladimir, Lapin, Sergey, Mazing, Alexandra, Verbitskaya, Elena, Trofimova, Tatiana, Krasnov, Vladimir, Shumilina, Maria, Skoromets, Alexander, Evdoshenko, Evgeniy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5643086/
https://www.ncbi.nlm.nih.gov/pubmed/29291134
http://dx.doi.org/10.1155/2017/8652463
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author Makshakov, Gleb
Magonov, Evgeniy
Totolyan, Natalia
Nazarov, Vladimir
Lapin, Sergey
Mazing, Alexandra
Verbitskaya, Elena
Trofimova, Tatiana
Krasnov, Vladimir
Shumilina, Maria
Skoromets, Alexander
Evdoshenko, Evgeniy
author_facet Makshakov, Gleb
Magonov, Evgeniy
Totolyan, Natalia
Nazarov, Vladimir
Lapin, Sergey
Mazing, Alexandra
Verbitskaya, Elena
Trofimova, Tatiana
Krasnov, Vladimir
Shumilina, Maria
Skoromets, Alexander
Evdoshenko, Evgeniy
author_sort Makshakov, Gleb
collection PubMed
description Leptomeningeal contrast enhancement (LMCE) on magnetic resonance imaging (MRI) is a newly recognized possible biomarker in multiple sclerosis (MS), associated with MS progression and cortical atrophy. In this study, we aimed to assess the prevalence of LMCE foci and their impact on neurodegeneration and disability. Materials. 54 patients with MS were included in the study. LMCE were detected with a 3 Tesla scanner on postcontrast fluid-attenuated inversion-recovery (FLAIR) sequence. Expanded Disability Status Scale (EDSS) score, number of relapses during 5 years from MS onset, and number of contrast-enhancing lesions on T1 weighted MRI were counted. Results. LMCE was detected in 41% (22/54) of patients. LMCE-positive patients had longer disease duration (p = 0,0098) and higher EDSS score (p = 0,039), but not a higher relapse rate (p = 0,091). No association of LMCE with higher frequency of contrast-enhancing lesions on T1-weighted images was detected (p = 0,3842). Analysis of covariates, adjusted for age, sex, and disease duration, revealed a significant effect of LMCE on the cortex volume (p = 0.043, F = 2.529), the total grey matter volume (p = 0.043, F = 2.54), and total ventricular volume (p = 0.039, F = 2.605). Conclusions. LMCE was shown to be an independent and significant biomarker of grey matter atrophy and disability in MS.
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spelling pubmed-56430862017-12-31 Leptomeningeal Contrast Enhancement Is Associated with Disability Progression and Grey Matter Atrophy in Multiple Sclerosis Makshakov, Gleb Magonov, Evgeniy Totolyan, Natalia Nazarov, Vladimir Lapin, Sergey Mazing, Alexandra Verbitskaya, Elena Trofimova, Tatiana Krasnov, Vladimir Shumilina, Maria Skoromets, Alexander Evdoshenko, Evgeniy Neurol Res Int Research Article Leptomeningeal contrast enhancement (LMCE) on magnetic resonance imaging (MRI) is a newly recognized possible biomarker in multiple sclerosis (MS), associated with MS progression and cortical atrophy. In this study, we aimed to assess the prevalence of LMCE foci and their impact on neurodegeneration and disability. Materials. 54 patients with MS were included in the study. LMCE were detected with a 3 Tesla scanner on postcontrast fluid-attenuated inversion-recovery (FLAIR) sequence. Expanded Disability Status Scale (EDSS) score, number of relapses during 5 years from MS onset, and number of contrast-enhancing lesions on T1 weighted MRI were counted. Results. LMCE was detected in 41% (22/54) of patients. LMCE-positive patients had longer disease duration (p = 0,0098) and higher EDSS score (p = 0,039), but not a higher relapse rate (p = 0,091). No association of LMCE with higher frequency of contrast-enhancing lesions on T1-weighted images was detected (p = 0,3842). Analysis of covariates, adjusted for age, sex, and disease duration, revealed a significant effect of LMCE on the cortex volume (p = 0.043, F = 2.529), the total grey matter volume (p = 0.043, F = 2.54), and total ventricular volume (p = 0.039, F = 2.605). Conclusions. LMCE was shown to be an independent and significant biomarker of grey matter atrophy and disability in MS. Hindawi 2017 2017-10-02 /pmc/articles/PMC5643086/ /pubmed/29291134 http://dx.doi.org/10.1155/2017/8652463 Text en Copyright © 2017 Gleb Makshakov et al. https://creativecommons.org/licenses/by/4.0/ 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
Makshakov, Gleb
Magonov, Evgeniy
Totolyan, Natalia
Nazarov, Vladimir
Lapin, Sergey
Mazing, Alexandra
Verbitskaya, Elena
Trofimova, Tatiana
Krasnov, Vladimir
Shumilina, Maria
Skoromets, Alexander
Evdoshenko, Evgeniy
Leptomeningeal Contrast Enhancement Is Associated with Disability Progression and Grey Matter Atrophy in Multiple Sclerosis
title Leptomeningeal Contrast Enhancement Is Associated with Disability Progression and Grey Matter Atrophy in Multiple Sclerosis
title_full Leptomeningeal Contrast Enhancement Is Associated with Disability Progression and Grey Matter Atrophy in Multiple Sclerosis
title_fullStr Leptomeningeal Contrast Enhancement Is Associated with Disability Progression and Grey Matter Atrophy in Multiple Sclerosis
title_full_unstemmed Leptomeningeal Contrast Enhancement Is Associated with Disability Progression and Grey Matter Atrophy in Multiple Sclerosis
title_short Leptomeningeal Contrast Enhancement Is Associated with Disability Progression and Grey Matter Atrophy in Multiple Sclerosis
title_sort leptomeningeal contrast enhancement is associated with disability progression and grey matter atrophy in multiple sclerosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5643086/
https://www.ncbi.nlm.nih.gov/pubmed/29291134
http://dx.doi.org/10.1155/2017/8652463
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