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Evidence of motor injury due to damaged corticospinal tract following acute hemorrhage in the basal ganglia region

The integrity of the corticospinal tract (CST) is significantly affected following basal ganglia haemorrhage. We aimed to assess the local features of CST and to effectively predict motor function by diffusion characteristics of CST in patients with motor injury following acute haemorrhage in the ac...

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Autores principales: Li, Jing, Wei, Xue Hu, Liu, Yong Kang, Chen, Ling Shan, Zhu, Zheng Qiu, Hou, Si Yuan, Fang, Xiao Kun, Wang, Zhong Qiu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7530683/
https://www.ncbi.nlm.nih.gov/pubmed/33004960
http://dx.doi.org/10.1038/s41598-020-73305-8
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author Li, Jing
Wei, Xue Hu
Liu, Yong Kang
Chen, Ling Shan
Zhu, Zheng Qiu
Hou, Si Yuan
Fang, Xiao Kun
Wang, Zhong Qiu
author_facet Li, Jing
Wei, Xue Hu
Liu, Yong Kang
Chen, Ling Shan
Zhu, Zheng Qiu
Hou, Si Yuan
Fang, Xiao Kun
Wang, Zhong Qiu
author_sort Li, Jing
collection PubMed
description The integrity of the corticospinal tract (CST) is significantly affected following basal ganglia haemorrhage. We aimed to assess the local features of CST and to effectively predict motor function by diffusion characteristics of CST in patients with motor injury following acute haemorrhage in the acute basal ganglia region. We recruited 37 patients with paresis of the lateral limbs caused by acute basal ganglia haemorrhage. Based on the automated fiber quantification method to track CST, assessed the character of each CST segment between the affected and contralateral sides, and correlated these with the Fugl–Meyer (FM) and Barthel Index (BI) scores at 6 months after onset. The fractional anisotropy (FA) values of the injured side of CST showed a significantly lower FA than the contralateral side along the tract profiles (p < 0.05, corrections for multiple comparisons). The FA values of each site at the internal capsule, closed corona radiata were positively correlated with the FM and BI score at 6 months after onset (p < 0.001, respectively). Our findings assessed the character of CST vividly in detail and dementated the primary sites of CST can predict the long-term outcome of motor function. This study may facilitate future clinical and cognitive studies of acute haemorrhage.
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spelling pubmed-75306832020-10-02 Evidence of motor injury due to damaged corticospinal tract following acute hemorrhage in the basal ganglia region Li, Jing Wei, Xue Hu Liu, Yong Kang Chen, Ling Shan Zhu, Zheng Qiu Hou, Si Yuan Fang, Xiao Kun Wang, Zhong Qiu Sci Rep Article The integrity of the corticospinal tract (CST) is significantly affected following basal ganglia haemorrhage. We aimed to assess the local features of CST and to effectively predict motor function by diffusion characteristics of CST in patients with motor injury following acute haemorrhage in the acute basal ganglia region. We recruited 37 patients with paresis of the lateral limbs caused by acute basal ganglia haemorrhage. Based on the automated fiber quantification method to track CST, assessed the character of each CST segment between the affected and contralateral sides, and correlated these with the Fugl–Meyer (FM) and Barthel Index (BI) scores at 6 months after onset. The fractional anisotropy (FA) values of the injured side of CST showed a significantly lower FA than the contralateral side along the tract profiles (p < 0.05, corrections for multiple comparisons). The FA values of each site at the internal capsule, closed corona radiata were positively correlated with the FM and BI score at 6 months after onset (p < 0.001, respectively). Our findings assessed the character of CST vividly in detail and dementated the primary sites of CST can predict the long-term outcome of motor function. This study may facilitate future clinical and cognitive studies of acute haemorrhage. Nature Publishing Group UK 2020-10-01 /pmc/articles/PMC7530683/ /pubmed/33004960 http://dx.doi.org/10.1038/s41598-020-73305-8 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Li, Jing
Wei, Xue Hu
Liu, Yong Kang
Chen, Ling Shan
Zhu, Zheng Qiu
Hou, Si Yuan
Fang, Xiao Kun
Wang, Zhong Qiu
Evidence of motor injury due to damaged corticospinal tract following acute hemorrhage in the basal ganglia region
title Evidence of motor injury due to damaged corticospinal tract following acute hemorrhage in the basal ganglia region
title_full Evidence of motor injury due to damaged corticospinal tract following acute hemorrhage in the basal ganglia region
title_fullStr Evidence of motor injury due to damaged corticospinal tract following acute hemorrhage in the basal ganglia region
title_full_unstemmed Evidence of motor injury due to damaged corticospinal tract following acute hemorrhage in the basal ganglia region
title_short Evidence of motor injury due to damaged corticospinal tract following acute hemorrhage in the basal ganglia region
title_sort evidence of motor injury due to damaged corticospinal tract following acute hemorrhage in the basal ganglia region
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7530683/
https://www.ncbi.nlm.nih.gov/pubmed/33004960
http://dx.doi.org/10.1038/s41598-020-73305-8
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