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Severe Lesions Involving Cortical Cholinergic Pathways Predict Poorer Functional Outcome in Acute Ischemic Stroke

BACKGROUND AND PURPOSE—: The aim of the study was to assess the effect of lesion severity in cortical cholinergic pathways in acute ischemic stroke patients on functional outcomes. METHODS—: The study sample consisted of 214 men (70.9%) and 88 women (29.1%) with acute ischemic stroke. We used the Ch...

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Autores principales: Qu, Jian-Feng, Chen, Yang-Kun, Luo, Gen-Pei, Zhao, Jiang-Hao, Zhong, Huo-Hua, Yin, Han-Peng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257508/
https://www.ncbi.nlm.nih.gov/pubmed/30571427
http://dx.doi.org/10.1161/STROKEAHA.118.023196
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author Qu, Jian-Feng
Chen, Yang-Kun
Luo, Gen-Pei
Zhao, Jiang-Hao
Zhong, Huo-Hua
Yin, Han-Peng
author_facet Qu, Jian-Feng
Chen, Yang-Kun
Luo, Gen-Pei
Zhao, Jiang-Hao
Zhong, Huo-Hua
Yin, Han-Peng
author_sort Qu, Jian-Feng
collection PubMed
description BACKGROUND AND PURPOSE—: The aim of the study was to assess the effect of lesion severity in cortical cholinergic pathways in acute ischemic stroke patients on functional outcomes. METHODS—: The study sample consisted of 214 men (70.9%) and 88 women (29.1%) with acute ischemic stroke. We used the Cholinergic Pathways Hyperintensities Scale (CHIPS) to assess the severity of lesions in cortical cholinergic pathways using brain magnetic resonance imaging. The other magnetic resonance imaging parameters included infarction, white matter lesions, and medial temporal lobe atrophy. Functional outcome was assessed using the Lawton activities of daily living (ADL) scale at 3 and 6 months after the index stroke. We also assessed disability status using the modified Rankin Scale. RESULTS—: Univariate analysis showed that patients with poor functional outcomes were older, more likely to be men, had a higher National Institutes of Health Stroke Scale (NIHSS) score on admission, and had more frequent histories of previous stroke and infection complications. They also had significantly more frequent cortical infarcts, left subcortical infarcts, a larger infarct volume, more severe medial temporal lobe atrophy, and periventricular hyperintensities, and higher CHIPS scores. In the multiple regression analysis, model 1 showed that age and NIHSS score on admission were significant predictors of poor ADL at 3 months, with an R(2) of 45.4% fitting the model. Age, NIHSS score on admission and stroke subtype were also significant predictors of poor ADL at 6 months, with an R(2) of 37.9% fitting the model. In model 2, sex, previous stroke, NIHSS score on admission, right cortical infarcts, left subcortical infarcts and CHIPS score were significant predictors for poor ADL at 3 months, with an R(2) of 53.5%. NIHSS score on admission, stroke subtype, and CHIPS score were significant predictors for poor ADL at 6 months, with an R(2) of 40.2%. After adjustment for confounders, CHIPS score was also a significant predictor for poor modified Rankin Scale, both at 3 and 6 months. Even after removing patients with moderate-to-severe white matter lesions, higher CHIPS scores still correlated with poorer ADL and modified Rankin Scale both at both 3 and 6 months. CONCLUSIONS—: In patients with acute ischemic stroke, cortical cholinergic pathways impairment is common, and the severity of lesions in the cortical cholinergic pathways may significantly predict a poorer functional outcome. CLINICAL TRIAL REGISTRATION—: URL: http://www.chictr.org.cn/index.aspx. Unique identifier: ChiCTR1800014982.
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spelling pubmed-62575082019-03-06 Severe Lesions Involving Cortical Cholinergic Pathways Predict Poorer Functional Outcome in Acute Ischemic Stroke Qu, Jian-Feng Chen, Yang-Kun Luo, Gen-Pei Zhao, Jiang-Hao Zhong, Huo-Hua Yin, Han-Peng Stroke Original Contributions BACKGROUND AND PURPOSE—: The aim of the study was to assess the effect of lesion severity in cortical cholinergic pathways in acute ischemic stroke patients on functional outcomes. METHODS—: The study sample consisted of 214 men (70.9%) and 88 women (29.1%) with acute ischemic stroke. We used the Cholinergic Pathways Hyperintensities Scale (CHIPS) to assess the severity of lesions in cortical cholinergic pathways using brain magnetic resonance imaging. The other magnetic resonance imaging parameters included infarction, white matter lesions, and medial temporal lobe atrophy. Functional outcome was assessed using the Lawton activities of daily living (ADL) scale at 3 and 6 months after the index stroke. We also assessed disability status using the modified Rankin Scale. RESULTS—: Univariate analysis showed that patients with poor functional outcomes were older, more likely to be men, had a higher National Institutes of Health Stroke Scale (NIHSS) score on admission, and had more frequent histories of previous stroke and infection complications. They also had significantly more frequent cortical infarcts, left subcortical infarcts, a larger infarct volume, more severe medial temporal lobe atrophy, and periventricular hyperintensities, and higher CHIPS scores. In the multiple regression analysis, model 1 showed that age and NIHSS score on admission were significant predictors of poor ADL at 3 months, with an R(2) of 45.4% fitting the model. Age, NIHSS score on admission and stroke subtype were also significant predictors of poor ADL at 6 months, with an R(2) of 37.9% fitting the model. In model 2, sex, previous stroke, NIHSS score on admission, right cortical infarcts, left subcortical infarcts and CHIPS score were significant predictors for poor ADL at 3 months, with an R(2) of 53.5%. NIHSS score on admission, stroke subtype, and CHIPS score were significant predictors for poor ADL at 6 months, with an R(2) of 40.2%. After adjustment for confounders, CHIPS score was also a significant predictor for poor modified Rankin Scale, both at 3 and 6 months. Even after removing patients with moderate-to-severe white matter lesions, higher CHIPS scores still correlated with poorer ADL and modified Rankin Scale both at both 3 and 6 months. CONCLUSIONS—: In patients with acute ischemic stroke, cortical cholinergic pathways impairment is common, and the severity of lesions in the cortical cholinergic pathways may significantly predict a poorer functional outcome. CLINICAL TRIAL REGISTRATION—: URL: http://www.chictr.org.cn/index.aspx. Unique identifier: ChiCTR1800014982. Lippincott Williams & Wilkins 2018-12 2018-11-01 /pmc/articles/PMC6257508/ /pubmed/30571427 http://dx.doi.org/10.1161/STROKEAHA.118.023196 Text en © 2018 The Authors. Stroke is published on behalf of the American Heart Association, Inc., by Wolters Kluwer Health, Inc. This is an open access article under the terms of the Creative Commons Attribution (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution, and reproduction in any medium, provided that the original work is properly cited.
spellingShingle Original Contributions
Qu, Jian-Feng
Chen, Yang-Kun
Luo, Gen-Pei
Zhao, Jiang-Hao
Zhong, Huo-Hua
Yin, Han-Peng
Severe Lesions Involving Cortical Cholinergic Pathways Predict Poorer Functional Outcome in Acute Ischemic Stroke
title Severe Lesions Involving Cortical Cholinergic Pathways Predict Poorer Functional Outcome in Acute Ischemic Stroke
title_full Severe Lesions Involving Cortical Cholinergic Pathways Predict Poorer Functional Outcome in Acute Ischemic Stroke
title_fullStr Severe Lesions Involving Cortical Cholinergic Pathways Predict Poorer Functional Outcome in Acute Ischemic Stroke
title_full_unstemmed Severe Lesions Involving Cortical Cholinergic Pathways Predict Poorer Functional Outcome in Acute Ischemic Stroke
title_short Severe Lesions Involving Cortical Cholinergic Pathways Predict Poorer Functional Outcome in Acute Ischemic Stroke
title_sort severe lesions involving cortical cholinergic pathways predict poorer functional outcome in acute ischemic stroke
topic Original Contributions
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257508/
https://www.ncbi.nlm.nih.gov/pubmed/30571427
http://dx.doi.org/10.1161/STROKEAHA.118.023196
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