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Plasma microRNA markers of upper limb recovery following human stroke

Preclinical investigators have implicated several microRNAs as regulators of gene expression promoting neural plasticity following experimental stroke in rodent models. Our goal was to determine whether similar microRNAs might be identifiable in plasma of humans with variable recovery from stroke. P...

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Autores principales: Edwardson, Matthew A., Zhong, Xiaogang, Fiandaca, Massimo S., Federoff, Howard J., Cheema, Amrita K., Dromerick, Alexander W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6105620/
https://www.ncbi.nlm.nih.gov/pubmed/30135469
http://dx.doi.org/10.1038/s41598-018-31020-5
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author Edwardson, Matthew A.
Zhong, Xiaogang
Fiandaca, Massimo S.
Federoff, Howard J.
Cheema, Amrita K.
Dromerick, Alexander W.
author_facet Edwardson, Matthew A.
Zhong, Xiaogang
Fiandaca, Massimo S.
Federoff, Howard J.
Cheema, Amrita K.
Dromerick, Alexander W.
author_sort Edwardson, Matthew A.
collection PubMed
description Preclinical investigators have implicated several microRNAs as regulators of gene expression promoting neural plasticity following experimental stroke in rodent models. Our goal was to determine whether similar microRNAs might be identifiable in plasma of humans with variable recovery from stroke. Plasma was collected 19 days post-stroke from 27 participants with mild-moderate upper extremity impairment enrolled in the Critical Periods After Stroke Study (CPASS). MicroRNA expression was assessed using TaqMan microRNA assays. Good clinical recovery was defined as ≥6 point change in the Action Research Arm Test (ARAT) score from baseline to 6 months, with 22 subjects showing good and 5 showing poor recovery. When comparing the good versus poor recovery groups, six microRNAs showed significantly decreased expression – miR-371-3p, miR-524, miR-520g, miR-1255A, miR-453, and miR-583, while 3 showed significantly increased expression - miR-941, miR-449b, and miR-581. MiR-371-3p and miR-941 have previously been associated with neural repair mechanisms; none of the significant microRNAs have previously been associated with stroke. The 9 microRNAs converge on pathways associated with axonal guidance, developmental biology, and cancer. We conclude that plasma microRNAs may be informative regarding human neural repair mechanisms during stroke recovery and probably differ from those seen in experimental stroke models.
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spelling pubmed-61056202018-08-27 Plasma microRNA markers of upper limb recovery following human stroke Edwardson, Matthew A. Zhong, Xiaogang Fiandaca, Massimo S. Federoff, Howard J. Cheema, Amrita K. Dromerick, Alexander W. Sci Rep Article Preclinical investigators have implicated several microRNAs as regulators of gene expression promoting neural plasticity following experimental stroke in rodent models. Our goal was to determine whether similar microRNAs might be identifiable in plasma of humans with variable recovery from stroke. Plasma was collected 19 days post-stroke from 27 participants with mild-moderate upper extremity impairment enrolled in the Critical Periods After Stroke Study (CPASS). MicroRNA expression was assessed using TaqMan microRNA assays. Good clinical recovery was defined as ≥6 point change in the Action Research Arm Test (ARAT) score from baseline to 6 months, with 22 subjects showing good and 5 showing poor recovery. When comparing the good versus poor recovery groups, six microRNAs showed significantly decreased expression – miR-371-3p, miR-524, miR-520g, miR-1255A, miR-453, and miR-583, while 3 showed significantly increased expression - miR-941, miR-449b, and miR-581. MiR-371-3p and miR-941 have previously been associated with neural repair mechanisms; none of the significant microRNAs have previously been associated with stroke. The 9 microRNAs converge on pathways associated with axonal guidance, developmental biology, and cancer. We conclude that plasma microRNAs may be informative regarding human neural repair mechanisms during stroke recovery and probably differ from those seen in experimental stroke models. Nature Publishing Group UK 2018-08-22 /pmc/articles/PMC6105620/ /pubmed/30135469 http://dx.doi.org/10.1038/s41598-018-31020-5 Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Edwardson, Matthew A.
Zhong, Xiaogang
Fiandaca, Massimo S.
Federoff, Howard J.
Cheema, Amrita K.
Dromerick, Alexander W.
Plasma microRNA markers of upper limb recovery following human stroke
title Plasma microRNA markers of upper limb recovery following human stroke
title_full Plasma microRNA markers of upper limb recovery following human stroke
title_fullStr Plasma microRNA markers of upper limb recovery following human stroke
title_full_unstemmed Plasma microRNA markers of upper limb recovery following human stroke
title_short Plasma microRNA markers of upper limb recovery following human stroke
title_sort plasma microrna markers of upper limb recovery following human stroke
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6105620/
https://www.ncbi.nlm.nih.gov/pubmed/30135469
http://dx.doi.org/10.1038/s41598-018-31020-5
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