Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/27274
Full metadata record
DC FieldValueLanguage
dc.contributor.authorLiu, F-
dc.contributor.authorChen, C-
dc.contributor.authorHong, W-
dc.contributor.authorBai, Z-
dc.contributor.authorWang, S-
dc.contributor.authorLu, H-
dc.contributor.authorLin, Q-
dc.contributor.authorZhao, Z-
dc.contributor.authorTang, C-
dc.date.accessioned2023-09-29T09:52:22Z-
dc.date.available2023-09-29T09:52:22Z-
dc.date.issued2022-01-10-
dc.identifierORCID iDs: Sizhong Wang https://orcid.org/0000-0002-9274-3447; Hanna Lu https://orcid.org/0000-0002-9090-258X; Chaozheng Tang https://orcid.org/0000-0002-2021-9988.-
dc.identifier.citationLiu, F. et al. (2022) 'Selectively disrupted sensorimotor circuits in chronic stroke with hand dysfunction', CNS Neuroscience and Therapeutics, 2022, 28 (5), pp. 677 - 689. doi: 10.1111/cns.13799.en_US
dc.identifier.issn1755-5930-
dc.identifier.urihttps://bura.brunel.ac.uk/handle/2438/27274-
dc.descriptionData availability statement: Data are available upon request from the corresponding authors.en_US
dc.description.abstractCopyright © 2022 The Authors. Aim: To investigate the directional and selective disconnection of the sensorimotor cortex (SMC) subregions in chronic stroke patients with hand dysfunction. Methods: We mapped the resting-state fMRI effective connectivity (EC) patterns for seven SMC subregions in each hemisphere of 65 chronic stroke patients and 40 healthy participants and correlated these patterns with paretic hand performance. Results: Compared with controls, patients demonstrated disrupted EC in the ipsilesional primary motor cortex_4p, ipsilesional primary somatosensory cortex_2 (PSC_2), and contralesional PSC_3a. Moreover, we found that EC values of the contralesional PSC_1 to contralesional precuneus, the ipsilesional inferior temporal gyrus to ipsilesional PSC_1, and the ipsilesional PSC_1 to contralesional postcentral gyrus were correlated with paretic hand performance across all patients. We further divided patients into partially (PPH) and completely (CPH) paretic hand subgroups. Compared with CPH patients, PPH patients demonstrated decreased EC in the ipsilesional premotor_6 and ipsilesional PSC_1. Interestingly, we found that paretic hand performance was positively correlated with seven sensorimotor circuits in PPH patients, while it was negatively correlated with five sensorimotor circuits in CPH patients. Conclusion: SMC neurocircuitry was selectively disrupted after chronic stroke and associated with diverse hand outcomes, which deepens the understanding of SMC reorganization.en_US
dc.description.sponsorshipNatural Science Foundation of Zhejiang Province. Grant Number: LGF19H270001; National Natural Science Foundation of China. Grant Number: 82002378; China Postdoctoral Science Foundation. Grant Number: 2020M671726; Shanghai Sailing Program. Grant Number: 20YF1445100.en_US
dc.format.extent677 - 689-
dc.format.mediumPrint-Electronic-
dc.language.isoen_USen_US
dc.publisherWileyen_US
dc.rightsCopyright © 2022 The Authors. CNS Neuroscience & Therapeutics published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.-
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.subjecteffective connectivityen_US
dc.subjectfunctional reorganizationen_US
dc.subjectGranger causality analysisen_US
dc.subjectresting-state functional magnetic resonance imagingen_US
dc.subjectstrokeen_US
dc.titleSelectively disrupted sensorimotor circuits in chronic stroke with hand dysfunctionen_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.1111/cns.13799-
dc.relation.isPartOfCNS Neuroscience and Therapeutics-
pubs.issue5-
pubs.publication-statusPublished-
pubs.volume28-
dc.identifier.eissn1755-5949-
dc.rights.holderThe Authors-
Appears in Collections:Dept of Health Sciences Research Papers

Files in This Item:
File Description SizeFormat 
FullText.pdfCopyright © 2022 The Authors. CNS Neuroscience & Therapeutics published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.2.65 MBAdobe PDFView/Open


This item is licensed under a Creative Commons License Creative Commons