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Strategic white matter injury associated with long‐term information processing speed deficits in mild traumatic brain injury

Deficits in information processing speed (IPS) are among the earliest and most prominent cognitive manifestations in mild traumatic brain injury (mTBI). We investigated the impact of white matter fiber location on IPS outcome in an individual basis assessment. A total of 112 acute mild TBI with all...

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Autores principales: Bai, Lijun, Bai, Guanghui, Wang, Shan, Yang, Xuefei, Gan, Shuoqiu, Jia, Xiaoyan, Yin, Bo, Yan, Zhihan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7502829/
https://www.ncbi.nlm.nih.gov/pubmed/32657510
http://dx.doi.org/10.1002/hbm.25135
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author Bai, Lijun
Bai, Guanghui
Wang, Shan
Yang, Xuefei
Gan, Shuoqiu
Jia, Xiaoyan
Yin, Bo
Yan, Zhihan
author_facet Bai, Lijun
Bai, Guanghui
Wang, Shan
Yang, Xuefei
Gan, Shuoqiu
Jia, Xiaoyan
Yin, Bo
Yan, Zhihan
author_sort Bai, Lijun
collection PubMed
description Deficits in information processing speed (IPS) are among the earliest and most prominent cognitive manifestations in mild traumatic brain injury (mTBI). We investigated the impact of white matter fiber location on IPS outcome in an individual basis assessment. A total of 112 acute mild TBI with all CT negative underwent brain DTI and blood sampling for inflammation cytokines within 7 days postinjury and 72 age‐ and sex matched healthy controls with same assessments were enrolled. IPS outcome was assessed by the trail making test at 6–12 month postinjury in mild TBI. Fractional anisotropy (FA) features were extracted using a novel lesion‐load analytical strategy to capture spatially heterogeneous white matter injuries and minimize implicit assumptions of uniform injury across diverse clinical presentations. Acute mild TBI exhibited a general pattern of increased and decreased FA in specific white matter tracts. The power of acute FA measures to identify patients developing IPS deficits with 92% accuracy and further improved to 96% accuracy by adding inflammation cytokines. The classifiers predicted individual's IPS and working memory ratings (r = .74 and .80, respectively, p < .001). The thalamo‐cortical circuits and commissural tracts projecting or connecting frontal regions became important predictors. This prognostic model was also verified by an independent replicate sample. Our findings highlighted damage to frontal interhemispheric and thalamic projection fiber tracts harboring frontal‐subcortical neuronal circuits as a predictor for processing speed performance in mild TBI.
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spelling pubmed-75028292020-09-28 Strategic white matter injury associated with long‐term information processing speed deficits in mild traumatic brain injury Bai, Lijun Bai, Guanghui Wang, Shan Yang, Xuefei Gan, Shuoqiu Jia, Xiaoyan Yin, Bo Yan, Zhihan Hum Brain Mapp Research Articles Deficits in information processing speed (IPS) are among the earliest and most prominent cognitive manifestations in mild traumatic brain injury (mTBI). We investigated the impact of white matter fiber location on IPS outcome in an individual basis assessment. A total of 112 acute mild TBI with all CT negative underwent brain DTI and blood sampling for inflammation cytokines within 7 days postinjury and 72 age‐ and sex matched healthy controls with same assessments were enrolled. IPS outcome was assessed by the trail making test at 6–12 month postinjury in mild TBI. Fractional anisotropy (FA) features were extracted using a novel lesion‐load analytical strategy to capture spatially heterogeneous white matter injuries and minimize implicit assumptions of uniform injury across diverse clinical presentations. Acute mild TBI exhibited a general pattern of increased and decreased FA in specific white matter tracts. The power of acute FA measures to identify patients developing IPS deficits with 92% accuracy and further improved to 96% accuracy by adding inflammation cytokines. The classifiers predicted individual's IPS and working memory ratings (r = .74 and .80, respectively, p < .001). The thalamo‐cortical circuits and commissural tracts projecting or connecting frontal regions became important predictors. This prognostic model was also verified by an independent replicate sample. Our findings highlighted damage to frontal interhemispheric and thalamic projection fiber tracts harboring frontal‐subcortical neuronal circuits as a predictor for processing speed performance in mild TBI. John Wiley & Sons, Inc. 2020-07-13 /pmc/articles/PMC7502829/ /pubmed/32657510 http://dx.doi.org/10.1002/hbm.25135 Text en © 2020 The Authors. Human Brain Mapping published by Wiley Periodicals LLC. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Bai, Lijun
Bai, Guanghui
Wang, Shan
Yang, Xuefei
Gan, Shuoqiu
Jia, Xiaoyan
Yin, Bo
Yan, Zhihan
Strategic white matter injury associated with long‐term information processing speed deficits in mild traumatic brain injury
title Strategic white matter injury associated with long‐term information processing speed deficits in mild traumatic brain injury
title_full Strategic white matter injury associated with long‐term information processing speed deficits in mild traumatic brain injury
title_fullStr Strategic white matter injury associated with long‐term information processing speed deficits in mild traumatic brain injury
title_full_unstemmed Strategic white matter injury associated with long‐term information processing speed deficits in mild traumatic brain injury
title_short Strategic white matter injury associated with long‐term information processing speed deficits in mild traumatic brain injury
title_sort strategic white matter injury associated with long‐term information processing speed deficits in mild traumatic brain injury
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7502829/
https://www.ncbi.nlm.nih.gov/pubmed/32657510
http://dx.doi.org/10.1002/hbm.25135
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