Please use this identifier to cite or link to this item: http://hdl.handle.net/1893/31795
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dc.contributor.authorGeva, Sharonen_UK
dc.contributor.authorJentschke, Sebastianen_UK
dc.contributor.authorArgyropoulos, Georgios P Den_UK
dc.contributor.authorChong, W Ken_UK
dc.contributor.authorGadian, David Gen_UK
dc.contributor.authorVargha-Khadem, Faranehen_UK
dc.date.accessioned2020-10-10T00:01:49Z-
dc.date.available2020-10-10T00:01:49Z-
dc.date.issued2020en_UK
dc.identifier.other102429en_UK
dc.identifier.urihttp://hdl.handle.net/1893/31795-
dc.description.abstractAcute sentinel hypoxia-ischaemia in neonates can target the hippocampus, mammillary bodies, thalamus, and the basal ganglia. Our previous work with paediatric patients with a history of hypoxia-ischaemia has revealed hippocampal and diencephalic damage that impacts cognitive memory. However, the structural and functional status of other brain regions vulnerable to hypoxia-ischaemia, such as the basal ganglia, has not been investigated in these patients. Furthermore, it is not known whether there are any behavioural sequelae of such damage, especially in patients with no diagnosis of neurological disorder. Based on the established role of the basal ganglia and the thalamus in movement coordination, we studied manual motor function in 20 participants exposed to neonatal hypoxia-ischaemia, and a group of 17 healthy controls of comparable age. The patients’ handwriting speed and accuracy was within the normal range (Detailed Assessment of Speed of Handwriting), and their movement adaptation learning (Rotary Pursuit task) was comparable to the control group’s performance. However, as a group, patients showed an impairment in the Grooved Pegboard task and a trend for impairment in speed of movement while performing the Rotary Pursuit task, suggesting that some patients have subtle deficits in fine, complex hand movements. Voxel-based morphometry and volumetry showed bilateral reduction in grey matter volume of the thalamus and caudate nucleus. Reduced volumes in the caudate nucleus correlated across patients with performance on the Grooved Pegboard task. In summary, the fine movement coordination deficit affecting the hand and the wrist in patients exposed to early hypoxic-ischaemic brain injury may be related to reduced volumes of the caudate nucleus, and consistent with anecdotal parental reports of clumsiness and coordination difficulties in this cohort.en_UK
dc.language.isoenen_UK
dc.publisherElsevier BVen_UK
dc.relationGeva S, Jentschke S, Argyropoulos GPD, Chong WK, Gadian DG & Vargha-Khadem F (2020) Volume reduction of caudate nucleus is associated with movement coordination deficits in patients with hippocampal atrophy due to perinatal hypoxia-ischaemia. NeuroImage: Clinical, 28, Art. No.: 102429. https://doi.org/10.1016/j.nicl.2020.102429en_UK
dc.rightsThis is an open access article distributed under the terms of the Creative Commons CC-BY license (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. You are not required to obtain permission to reuse this article.en_UK
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_UK
dc.subjectHypoxia-ischaemiaen_UK
dc.subjectMotor controlen_UK
dc.subjectVoxel-based morphometryen_UK
dc.subjectCaudate nucleusen_UK
dc.subjectThalamusen_UK
dc.titleVolume reduction of caudate nucleus is associated with movement coordination deficits in patients with hippocampal atrophy due to perinatal hypoxia-ischaemiaen_UK
dc.typeJournal Articleen_UK
dc.identifier.doi10.1016/j.nicl.2020.102429en_UK
dc.identifier.pmid33010533en_UK
dc.citation.jtitleNeuroImage: Clinicalen_UK
dc.citation.issn2213-1582en_UK
dc.citation.volume28en_UK
dc.citation.publicationstatusPublisheden_UK
dc.citation.peerreviewedRefereeden_UK
dc.type.statusVoR - Version of Recorden_UK
dc.contributor.funderMedical Research Councilen_UK
dc.contributor.funderUK Clinical Research Networken_UK
dc.contributor.funderMedical Research Councilen_UK
dc.author.emailgeorgios.argyropoulos@stir.ac.uken_UK
dc.citation.date15/09/2020en_UK
dc.contributor.affiliationUniversity College Londonen_UK
dc.contributor.affiliationUniversity College Londonen_UK
dc.contributor.affiliationUniversity College Londonen_UK
dc.contributor.affiliationUniversity College Londonen_UK
dc.contributor.affiliationUniversity College Londonen_UK
dc.contributor.affiliationUniversity College Londonen_UK
dc.identifier.isiWOS:000600619100072en_UK
dc.identifier.scopusid2-s2.0-85091766603en_UK
dc.identifier.wtid1670495en_UK
dc.contributor.orcid0000-0001-8267-6861en_UK
dc.date.accepted2020-09-08en_UK
dcterms.dateAccepted2020-09-08en_UK
dc.date.filedepositdate2020-10-09en_UK
rioxxterms.apcnot requireden_UK
rioxxterms.typeJournal Article/Reviewen_UK
rioxxterms.versionVoRen_UK
local.rioxx.authorGeva, Sharon|en_UK
local.rioxx.authorJentschke, Sebastian|en_UK
local.rioxx.authorArgyropoulos, Georgios P D|0000-0001-8267-6861en_UK
local.rioxx.authorChong, W K|en_UK
local.rioxx.authorGadian, David G|en_UK
local.rioxx.authorVargha-Khadem, Faraneh|en_UK
local.rioxx.projectG0300117-65439|Medical Research Council|http://dx.doi.org/10.13039/501100000265en_UK
local.rioxx.projectProject ID unknown|UK Clinical Research Network|en_UK
local.rioxx.projectG1002276-98624|Medical Research Council|http://dx.doi.org/10.13039/501100000265en_UK
local.rioxx.freetoreaddate2020-10-09en_UK
local.rioxx.licencehttp://creativecommons.org/licenses/by/4.0/|2020-10-09|en_UK
local.rioxx.filename1-s2.0-S2213158220302667-main.pdfen_UK
local.rioxx.filecount1en_UK
local.rioxx.source2213-1582en_UK
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