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Clinical and neuroimaging factors associated with aphasia severity in stroke patients: diffusion tensor imaging study

This study investigated factors associated with aphasia severity at both 2 weeks and 3 months after stroke using demographic and clinical variables, brain diffusion tensor imaging (DTI) parameters, and lesion volume measurements. Patients with left hemisphere stroke were assessed at 2 weeks (n = 68)...

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Autores principales: Lee, Sekwang, Na, Yoonhye, Tae, Woo-Suk, Pyun, Sung-Bom
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7393375/
https://www.ncbi.nlm.nih.gov/pubmed/32733102
http://dx.doi.org/10.1038/s41598-020-69741-1
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author Lee, Sekwang
Na, Yoonhye
Tae, Woo-Suk
Pyun, Sung-Bom
author_facet Lee, Sekwang
Na, Yoonhye
Tae, Woo-Suk
Pyun, Sung-Bom
author_sort Lee, Sekwang
collection PubMed
description This study investigated factors associated with aphasia severity at both 2 weeks and 3 months after stroke using demographic and clinical variables, brain diffusion tensor imaging (DTI) parameters, and lesion volume measurements. Patients with left hemisphere stroke were assessed at 2 weeks (n = 68) and at 3 months (n = 20) after stroke. Demographic, clinical, and neuroimaging data were collected; language functions were assessed using the Western Aphasia Battery. For neuroimaging, DTI parameters, including the laterality index (LI) of fractional anisotropy (FA), axial diffusivity (AD), radial diffusivity, mean diffusivity and fibre density (FD) of the arcuate fasciculus (AF), and lesion volume, were measured. Lesion volume, cortical involvement, and the National Institutes of Health Stroke Scale score significantly predicted aphasia severity at 2 weeks after stroke, whereas the aphasia quotient and presence of depression during the early subacute stage were significant predictors at 3 months after stroke. According to Pearson correlation, LI-AD and LI-FD were significantly correlated with the aphasia quotient 2 weeks after ischaemic stroke, and the LI-FA was significantly correlated with the aphasia quotient 2 weeks after haemorrhagic stroke, suggesting that the extent and mechanism of AF injuries differ between ischaemic and haemorrhagic strokes. These differences may contribute to aphasia severity.
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spelling pubmed-73933752020-08-03 Clinical and neuroimaging factors associated with aphasia severity in stroke patients: diffusion tensor imaging study Lee, Sekwang Na, Yoonhye Tae, Woo-Suk Pyun, Sung-Bom Sci Rep Article This study investigated factors associated with aphasia severity at both 2 weeks and 3 months after stroke using demographic and clinical variables, brain diffusion tensor imaging (DTI) parameters, and lesion volume measurements. Patients with left hemisphere stroke were assessed at 2 weeks (n = 68) and at 3 months (n = 20) after stroke. Demographic, clinical, and neuroimaging data were collected; language functions were assessed using the Western Aphasia Battery. For neuroimaging, DTI parameters, including the laterality index (LI) of fractional anisotropy (FA), axial diffusivity (AD), radial diffusivity, mean diffusivity and fibre density (FD) of the arcuate fasciculus (AF), and lesion volume, were measured. Lesion volume, cortical involvement, and the National Institutes of Health Stroke Scale score significantly predicted aphasia severity at 2 weeks after stroke, whereas the aphasia quotient and presence of depression during the early subacute stage were significant predictors at 3 months after stroke. According to Pearson correlation, LI-AD and LI-FD were significantly correlated with the aphasia quotient 2 weeks after ischaemic stroke, and the LI-FA was significantly correlated with the aphasia quotient 2 weeks after haemorrhagic stroke, suggesting that the extent and mechanism of AF injuries differ between ischaemic and haemorrhagic strokes. These differences may contribute to aphasia severity. Nature Publishing Group UK 2020-07-30 /pmc/articles/PMC7393375/ /pubmed/32733102 http://dx.doi.org/10.1038/s41598-020-69741-1 Text en © The Author(s) 2020 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
Lee, Sekwang
Na, Yoonhye
Tae, Woo-Suk
Pyun, Sung-Bom
Clinical and neuroimaging factors associated with aphasia severity in stroke patients: diffusion tensor imaging study
title Clinical and neuroimaging factors associated with aphasia severity in stroke patients: diffusion tensor imaging study
title_full Clinical and neuroimaging factors associated with aphasia severity in stroke patients: diffusion tensor imaging study
title_fullStr Clinical and neuroimaging factors associated with aphasia severity in stroke patients: diffusion tensor imaging study
title_full_unstemmed Clinical and neuroimaging factors associated with aphasia severity in stroke patients: diffusion tensor imaging study
title_short Clinical and neuroimaging factors associated with aphasia severity in stroke patients: diffusion tensor imaging study
title_sort clinical and neuroimaging factors associated with aphasia severity in stroke patients: diffusion tensor imaging study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7393375/
https://www.ncbi.nlm.nih.gov/pubmed/32733102
http://dx.doi.org/10.1038/s41598-020-69741-1
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