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Multimodal magnetic resonance imaging in relation to cognitive impairment in neuromyelitis optica spectrum disorder

Cognitive impairment (CI) is reported in 29–57% of patients with neuromyelitis optica spectrum disorder (NMOSD). However, the pathophysiology underlying CI in NMOSD is poorly understood. The present study aims to investigate the predictive values of various conventional and quantitative MRI paramete...

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Autores principales: Kim, Su-Hyun, Park, Eun Young, Park, Boram, Hyun, Jae-Won, Park, Na Young, Joung, AeRan, Lee, Sang Hyun, Kim, Ho Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5569012/
https://www.ncbi.nlm.nih.gov/pubmed/28835657
http://dx.doi.org/10.1038/s41598-017-08889-9
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author Kim, Su-Hyun
Park, Eun Young
Park, Boram
Hyun, Jae-Won
Park, Na Young
Joung, AeRan
Lee, Sang Hyun
Kim, Ho Jin
author_facet Kim, Su-Hyun
Park, Eun Young
Park, Boram
Hyun, Jae-Won
Park, Na Young
Joung, AeRan
Lee, Sang Hyun
Kim, Ho Jin
author_sort Kim, Su-Hyun
collection PubMed
description Cognitive impairment (CI) is reported in 29–57% of patients with neuromyelitis optica spectrum disorder (NMOSD). However, the pathophysiology underlying CI in NMOSD is poorly understood. The present study aims to investigate the predictive values of various conventional and quantitative MRI parameters for cognitive performance in patients with NMOSD. Neurological assessment and conventional, diffusion tensor, and volumetric MRI sequences were collected form 73 patients with NMOSD and 44 healthy controls (HCs). Patients with ≥3 failed tests were considered to have CI. Brain lesion load, gray matter (GM) and white matter (WM) atrophy, deep GM (DGM) atrophy, cortical thickness, and diffuse microstructural WM damage were assessed. Twenty-three (32%) patients with NMOSD had CI. Compared to cognitively preserved (CP) individuals, patients with CI had atrophy in the WM, thalamus, and caudate, decreased fractional anisotropy (FA) and increased mean diffusivity in their WM. A multivariate model indicated that mean FA values in the WM and volume in the nucleus accumbens (NAc) were associated with overall cognition (p = 0.002 and p = 0.008, respectively). Diffuse microstructural damage in the WM and DGM atrophy in the NAc are the strongest predictors of cognitive impairment in patients with NMOSD.
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spelling pubmed-55690122017-09-01 Multimodal magnetic resonance imaging in relation to cognitive impairment in neuromyelitis optica spectrum disorder Kim, Su-Hyun Park, Eun Young Park, Boram Hyun, Jae-Won Park, Na Young Joung, AeRan Lee, Sang Hyun Kim, Ho Jin Sci Rep Article Cognitive impairment (CI) is reported in 29–57% of patients with neuromyelitis optica spectrum disorder (NMOSD). However, the pathophysiology underlying CI in NMOSD is poorly understood. The present study aims to investigate the predictive values of various conventional and quantitative MRI parameters for cognitive performance in patients with NMOSD. Neurological assessment and conventional, diffusion tensor, and volumetric MRI sequences were collected form 73 patients with NMOSD and 44 healthy controls (HCs). Patients with ≥3 failed tests were considered to have CI. Brain lesion load, gray matter (GM) and white matter (WM) atrophy, deep GM (DGM) atrophy, cortical thickness, and diffuse microstructural WM damage were assessed. Twenty-three (32%) patients with NMOSD had CI. Compared to cognitively preserved (CP) individuals, patients with CI had atrophy in the WM, thalamus, and caudate, decreased fractional anisotropy (FA) and increased mean diffusivity in their WM. A multivariate model indicated that mean FA values in the WM and volume in the nucleus accumbens (NAc) were associated with overall cognition (p = 0.002 and p = 0.008, respectively). Diffuse microstructural damage in the WM and DGM atrophy in the NAc are the strongest predictors of cognitive impairment in patients with NMOSD. Nature Publishing Group UK 2017-08-23 /pmc/articles/PMC5569012/ /pubmed/28835657 http://dx.doi.org/10.1038/s41598-017-08889-9 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Kim, Su-Hyun
Park, Eun Young
Park, Boram
Hyun, Jae-Won
Park, Na Young
Joung, AeRan
Lee, Sang Hyun
Kim, Ho Jin
Multimodal magnetic resonance imaging in relation to cognitive impairment in neuromyelitis optica spectrum disorder
title Multimodal magnetic resonance imaging in relation to cognitive impairment in neuromyelitis optica spectrum disorder
title_full Multimodal magnetic resonance imaging in relation to cognitive impairment in neuromyelitis optica spectrum disorder
title_fullStr Multimodal magnetic resonance imaging in relation to cognitive impairment in neuromyelitis optica spectrum disorder
title_full_unstemmed Multimodal magnetic resonance imaging in relation to cognitive impairment in neuromyelitis optica spectrum disorder
title_short Multimodal magnetic resonance imaging in relation to cognitive impairment in neuromyelitis optica spectrum disorder
title_sort multimodal magnetic resonance imaging in relation to cognitive impairment in neuromyelitis optica spectrum disorder
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5569012/
https://www.ncbi.nlm.nih.gov/pubmed/28835657
http://dx.doi.org/10.1038/s41598-017-08889-9
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