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A Clinical Research Study of Cognitive Dysfunction and Affective Impairment after Isolated Brainstem Stroke

Although the function of the cerebellum in neurocognition has been well-documented, the similar role of the brainstem has yet to be fully elucidated. This clinical research study aimed to combine data relating to neuropsychological assessments and P300 to explore cognitive dysfunction and affective...

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Autores principales: Fu, Xiujuan, Lu, Zuneng, Wang, Yan, Huang, Lifang, Wang, Xi, Zhang, Hong, Xiao, Zheman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5742202/
https://www.ncbi.nlm.nih.gov/pubmed/29311895
http://dx.doi.org/10.3389/fnagi.2017.00400
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author Fu, Xiujuan
Lu, Zuneng
Wang, Yan
Huang, Lifang
Wang, Xi
Zhang, Hong
Xiao, Zheman
author_facet Fu, Xiujuan
Lu, Zuneng
Wang, Yan
Huang, Lifang
Wang, Xi
Zhang, Hong
Xiao, Zheman
author_sort Fu, Xiujuan
collection PubMed
description Although the function of the cerebellum in neurocognition has been well-documented, the similar role of the brainstem has yet to be fully elucidated. This clinical research study aimed to combine data relating to neuropsychological assessments and P300 to explore cognitive dysfunction and affective impairment following brainstem stroke. Thirty-four patients with isolated brainstem stroke and twenty-six healthy controls were recruited; for each patient, we collated data pertaining to the P300, Addenbrooke's Cognitive Examination III (ACE-III), Montreal Cognitive Assessment Chinese version (MoCA), trail-making test (TMT), Symbol Digit Modalities Test (SDMT), Wechsler Adult Intelligence Scale-Digit Spans (DS), Stroop test, Self Rating Depression Scale (SDS), and Self Rating Anxiety Scale (SAS). Significance was analyzed using an independent T-test or the Mann-Whitney U-test. Correlation was analyzed using Pearson's correlation analysis or Spearman's correlation analysis. Collectively, data revealed that brainstem stroke caused mild cognitive impairment (MCI), and that visuospatial, attention, linguistic, and emotional disturbances may occur after isolated brainstem stroke. Cognitive decline was linked to P300 latency, ACE-III, and MoCA; P300 latency was correlated with ACE-III. Patients with right brainstem lesions were more likely to suffer memory decline. The present study provides initial data relating to the role of the brainstem in neurocognition, and will be useful for further understanding of vascular cognitive and affective impairment.
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spelling pubmed-57422022018-01-08 A Clinical Research Study of Cognitive Dysfunction and Affective Impairment after Isolated Brainstem Stroke Fu, Xiujuan Lu, Zuneng Wang, Yan Huang, Lifang Wang, Xi Zhang, Hong Xiao, Zheman Front Aging Neurosci Neuroscience Although the function of the cerebellum in neurocognition has been well-documented, the similar role of the brainstem has yet to be fully elucidated. This clinical research study aimed to combine data relating to neuropsychological assessments and P300 to explore cognitive dysfunction and affective impairment following brainstem stroke. Thirty-four patients with isolated brainstem stroke and twenty-six healthy controls were recruited; for each patient, we collated data pertaining to the P300, Addenbrooke's Cognitive Examination III (ACE-III), Montreal Cognitive Assessment Chinese version (MoCA), trail-making test (TMT), Symbol Digit Modalities Test (SDMT), Wechsler Adult Intelligence Scale-Digit Spans (DS), Stroop test, Self Rating Depression Scale (SDS), and Self Rating Anxiety Scale (SAS). Significance was analyzed using an independent T-test or the Mann-Whitney U-test. Correlation was analyzed using Pearson's correlation analysis or Spearman's correlation analysis. Collectively, data revealed that brainstem stroke caused mild cognitive impairment (MCI), and that visuospatial, attention, linguistic, and emotional disturbances may occur after isolated brainstem stroke. Cognitive decline was linked to P300 latency, ACE-III, and MoCA; P300 latency was correlated with ACE-III. Patients with right brainstem lesions were more likely to suffer memory decline. The present study provides initial data relating to the role of the brainstem in neurocognition, and will be useful for further understanding of vascular cognitive and affective impairment. Frontiers Media S.A. 2017-12-19 /pmc/articles/PMC5742202/ /pubmed/29311895 http://dx.doi.org/10.3389/fnagi.2017.00400 Text en Copyright © 2017 Fu, Lu, Wang, Huang, Wang, Zhang and Xiao. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Fu, Xiujuan
Lu, Zuneng
Wang, Yan
Huang, Lifang
Wang, Xi
Zhang, Hong
Xiao, Zheman
A Clinical Research Study of Cognitive Dysfunction and Affective Impairment after Isolated Brainstem Stroke
title A Clinical Research Study of Cognitive Dysfunction and Affective Impairment after Isolated Brainstem Stroke
title_full A Clinical Research Study of Cognitive Dysfunction and Affective Impairment after Isolated Brainstem Stroke
title_fullStr A Clinical Research Study of Cognitive Dysfunction and Affective Impairment after Isolated Brainstem Stroke
title_full_unstemmed A Clinical Research Study of Cognitive Dysfunction and Affective Impairment after Isolated Brainstem Stroke
title_short A Clinical Research Study of Cognitive Dysfunction and Affective Impairment after Isolated Brainstem Stroke
title_sort clinical research study of cognitive dysfunction and affective impairment after isolated brainstem stroke
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5742202/
https://www.ncbi.nlm.nih.gov/pubmed/29311895
http://dx.doi.org/10.3389/fnagi.2017.00400
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