Please use this identifier to cite or link to this item: https://hdl.handle.net/1959.11/64379
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dc.contributor.authorWilliams, Rebecca Jen
dc.contributor.authorGoodyear, Bradley Gen
dc.contributor.authorPeca, Stefanoen
dc.contributor.authorMcCreary, Cheryl Ren
dc.contributor.authorFrayne, Richarden
dc.contributor.authorSmith, Eric Een
dc.contributor.authorPike, G Bruceen
dc.date.accessioned2025-01-08T00:55:13Z-
dc.date.available2025-01-08T00:55:13Z-
dc.date.issued2017-02-01-
dc.identifier.citationJournal of Cerebral Blood Flow and Metabolism, 37(10), p. 3433-3445en
dc.identifier.issn1559-7016en
dc.identifier.issn0271-678Xen
dc.identifier.urihttps://hdl.handle.net/1959.11/64379-
dc.description.abstract<p>Cerebral amyloid angiopathy (CAA) is a small-vessel disease preferentially affecting posterior brain regions. Recent evidence has demonstrated the efficacy of functional MRI in detecting CAA-related neurovascular injury, however, it is unknown whether such perturbations are associated with changes in the hemodynamic response function (HRF). Here we estimated HRFs from two different brain regions from block design activation data, in light of recent findings demonstrating how block designs can accurately reflect HRF parameter estimates while maximizing signal detection. Patients with a diagnosis of probable CAA and healthy controls performed motor and visual stimulation tasks. Time-topeak (TTP), full-width at half-maximum (FWHM), and area under the curve (AUC) of the estimated HRFs were compared between groups and to MRI features associated with CAA including cerebral microbleed (CMB) count. Motor HRFs in CAA patients showed significantly wider FWHM (<i>P</i> = 0.006) and delayed TTP (<i>P</i> = 0.03) compared to controls. In the patient group, visual HRF FWHM was positively associated with CMB count (<i>P</i> = 0.03). These findings indicate that hemodynamic abnormalities in patients with CAA may be reflected in HRFs estimated from block designs across different brain regions. Moreover, visual FWHM may be linked to structural MR indications associated with CAA.</p>en
dc.languageenen
dc.publisherSage Publications Ltden
dc.relation.ispartofJournal of Cerebral Blood Flow and Metabolismen
dc.titleIdentification of neurovascular changes associated with cerebral amyloid angiopathy from subject-specific hemodynamic response functionsen
dc.typeJournal Articleen
dc.identifier.doi10.1177/0271678x17691056en
dcterms.accessRightsBronzeen
local.contributor.firstnameRebecca Jen
local.contributor.firstnameBradley Gen
local.contributor.firstnameStefanoen
local.contributor.firstnameCheryl Ren
local.contributor.firstnameRicharden
local.contributor.firstnameEric Een
local.contributor.firstnameG Bruceen
local.profile.schoolSchool of Science and Technologyen
local.profile.emailrwilli90@une.edu.auen
local.output.categoryC1en
local.record.placeauen
local.record.institutionUniversity of New Englanden
local.publisher.placeUnited Kingdomen
local.format.startpage3433en
local.format.endpage3445en
local.peerreviewedYesen
local.identifier.volume37en
local.identifier.issue10en
local.access.fulltextYesen
local.contributor.lastnameWilliamsen
local.contributor.lastnameGoodyearen
local.contributor.lastnamePecaen
local.contributor.lastnameMcCrearyen
local.contributor.lastnameFrayneen
local.contributor.lastnameSmithen
local.contributor.lastnamePikeen
dc.identifier.staffune-id:rwilli90en
local.profile.orcid0000-0002-8949-1197en
local.profile.roleauthoren
local.profile.roleauthoren
local.profile.roleauthoren
local.profile.roleauthoren
local.profile.roleauthoren
local.profile.roleauthoren
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local.identifier.unepublicationidune:1959.11/64379en
dc.identifier.academiclevelAcademicen
dc.identifier.academiclevelAcademicen
dc.identifier.academiclevelAcademicen
dc.identifier.academiclevelAcademicen
dc.identifier.academiclevelAcademicen
dc.identifier.academiclevelAcademicen
dc.identifier.academiclevelAcademicen
local.title.maintitleIdentification of neurovascular changes associated with cerebral amyloid angiopathy from subject-specific hemodynamic response functionsen
local.relation.fundingsourcenoteThe study was funded by operating grants from the Canadian Stroke Network, Heart and Stroke Foundation of Canada, and the Alzheimer Society of Canada. RJW received funding from the NSERC CREATE International and Industrial Imaging Training Program. GBP received funding from Campus Alberta Innovates and CIHR FDN-143290en
local.output.categorydescriptionC1 Refereed Article in a Scholarly Journalen
local.search.authorWilliams, Rebecca Jen
local.search.authorGoodyear, Bradley Gen
local.search.authorPeca, Stefanoen
local.search.authorMcCreary, Cheryl Ren
local.search.authorFrayne, Richarden
local.search.authorSmith, Eric Een
local.search.authorPike, G Bruceen
local.open.fileurlhttps://rune.une.edu.au/web/retrieve/e1a84c3d-dd75-4fdf-8240-43d64be5b695en
local.uneassociationNoen
local.atsiresearchNoen
local.sensitive.culturalNoen
local.year.published2017en
local.fileurl.openhttps://rune.une.edu.au/web/retrieve/e1a84c3d-dd75-4fdf-8240-43d64be5b695en
local.fileurl.closedpublishedhttps://rune.une.edu.au/web/retrieve/e1a84c3d-dd75-4fdf-8240-43d64be5b695en
local.subject.for20203209 Neurosciencesen
local.profile.affiliationtypeExternal Affiliationen
local.profile.affiliationtypeExternal Affiliationen
local.profile.affiliationtypeExternal Affiliationen
local.profile.affiliationtypeExternal Affiliationen
local.profile.affiliationtypeExternal Affiliationen
local.profile.affiliationtypeExternal Affiliationen
local.profile.affiliationtypeExternal Affiliationen
local.date.moved2025-01-08en
Appears in Collections:Journal Article
School of Science and Technology
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