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Interhemispheric Pathways Are Important for Motor Outcome in Individuals with Chronic and Severe Upper Limb Impairment Post Stroke

BACKGROUND: Severity of arm impairment alone does not explain motor outcomes in people with severe impairment post stroke. OBJECTIVE: Define the contribution of brain biomarkers to upper limb motor outcomes in people with severe arm impairment post stroke. METHODS: Paretic arm impairment (Fugl-Meyer...

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Autores principales: Hayward, Kathryn S., Neva, Jason L., Mang, Cameron S., Peters, Sue, Wadden, Katie P., Ferris, Jennifer K., Boyd, Lara A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5733869/
https://www.ncbi.nlm.nih.gov/pubmed/29348943
http://dx.doi.org/10.1155/2017/4281532
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author Hayward, Kathryn S.
Neva, Jason L.
Mang, Cameron S.
Peters, Sue
Wadden, Katie P.
Ferris, Jennifer K.
Boyd, Lara A.
author_facet Hayward, Kathryn S.
Neva, Jason L.
Mang, Cameron S.
Peters, Sue
Wadden, Katie P.
Ferris, Jennifer K.
Boyd, Lara A.
author_sort Hayward, Kathryn S.
collection PubMed
description BACKGROUND: Severity of arm impairment alone does not explain motor outcomes in people with severe impairment post stroke. OBJECTIVE: Define the contribution of brain biomarkers to upper limb motor outcomes in people with severe arm impairment post stroke. METHODS: Paretic arm impairment (Fugl-Meyer upper limb, FM-UL) and function (Wolf Motor Function Test rate, WMFT-rate) were measured in 15 individuals with severe (FM-UL ≤ 30/66) and 14 with mild–moderate (FM-UL > 40/66) impairment. Transcranial magnetic stimulation and diffusion weight imaging indexed structure and function of the corticospinal tract and corpus callosum. Separate models of the relationship between possible biomarkers and motor outcomes at a single chronic (≥6 months) time point post stroke were performed. RESULTS: Age (ΔR(2)0.365, p = 0.017) and ipsilesional-transcallosal inhibition (ΔR(2)0.182, p = 0.048) explained a 54.7% (p = 0.009) variance in paretic WMFT-rate. Prefrontal corpus callous fractional anisotropy (PF-CC FA) alone explained 49.3% (p = 0.007) variance in FM-UL outcome. The same models did not explain significant variance in mild–moderate stroke. In the severe group, k-means cluster analysis of PF-CC FA distinguished two subgroups, separated by a clinically meaningful and significant difference in motor impairment (p = 0.049) and function (p = 0.006) outcomes. CONCLUSION: Corpus callosum function and structure were identified as possible biomarkers of motor outcome in people with chronic and severe arm impairment.
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spelling pubmed-57338692018-01-18 Interhemispheric Pathways Are Important for Motor Outcome in Individuals with Chronic and Severe Upper Limb Impairment Post Stroke Hayward, Kathryn S. Neva, Jason L. Mang, Cameron S. Peters, Sue Wadden, Katie P. Ferris, Jennifer K. Boyd, Lara A. Neural Plast Research Article BACKGROUND: Severity of arm impairment alone does not explain motor outcomes in people with severe impairment post stroke. OBJECTIVE: Define the contribution of brain biomarkers to upper limb motor outcomes in people with severe arm impairment post stroke. METHODS: Paretic arm impairment (Fugl-Meyer upper limb, FM-UL) and function (Wolf Motor Function Test rate, WMFT-rate) were measured in 15 individuals with severe (FM-UL ≤ 30/66) and 14 with mild–moderate (FM-UL > 40/66) impairment. Transcranial magnetic stimulation and diffusion weight imaging indexed structure and function of the corticospinal tract and corpus callosum. Separate models of the relationship between possible biomarkers and motor outcomes at a single chronic (≥6 months) time point post stroke were performed. RESULTS: Age (ΔR(2)0.365, p = 0.017) and ipsilesional-transcallosal inhibition (ΔR(2)0.182, p = 0.048) explained a 54.7% (p = 0.009) variance in paretic WMFT-rate. Prefrontal corpus callous fractional anisotropy (PF-CC FA) alone explained 49.3% (p = 0.007) variance in FM-UL outcome. The same models did not explain significant variance in mild–moderate stroke. In the severe group, k-means cluster analysis of PF-CC FA distinguished two subgroups, separated by a clinically meaningful and significant difference in motor impairment (p = 0.049) and function (p = 0.006) outcomes. CONCLUSION: Corpus callosum function and structure were identified as possible biomarkers of motor outcome in people with chronic and severe arm impairment. Hindawi 2017 2017-11-16 /pmc/articles/PMC5733869/ /pubmed/29348943 http://dx.doi.org/10.1155/2017/4281532 Text en Copyright © 2017 Kathryn S. Hayward et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Hayward, Kathryn S.
Neva, Jason L.
Mang, Cameron S.
Peters, Sue
Wadden, Katie P.
Ferris, Jennifer K.
Boyd, Lara A.
Interhemispheric Pathways Are Important for Motor Outcome in Individuals with Chronic and Severe Upper Limb Impairment Post Stroke
title Interhemispheric Pathways Are Important for Motor Outcome in Individuals with Chronic and Severe Upper Limb Impairment Post Stroke
title_full Interhemispheric Pathways Are Important for Motor Outcome in Individuals with Chronic and Severe Upper Limb Impairment Post Stroke
title_fullStr Interhemispheric Pathways Are Important for Motor Outcome in Individuals with Chronic and Severe Upper Limb Impairment Post Stroke
title_full_unstemmed Interhemispheric Pathways Are Important for Motor Outcome in Individuals with Chronic and Severe Upper Limb Impairment Post Stroke
title_short Interhemispheric Pathways Are Important for Motor Outcome in Individuals with Chronic and Severe Upper Limb Impairment Post Stroke
title_sort interhemispheric pathways are important for motor outcome in individuals with chronic and severe upper limb impairment post stroke
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5733869/
https://www.ncbi.nlm.nih.gov/pubmed/29348943
http://dx.doi.org/10.1155/2017/4281532
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