Please use this identifier to cite or link to this item: https://hdl.handle.net/1959.11/64369
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dc.contributor.authorPearson, Michael Jen
dc.contributor.authorWagstaff, Ruthen
dc.contributor.authorWilliams, Rebecca Jen
dc.date.accessioned2025-01-07T22:18:40Z-
dc.date.available2025-01-07T22:18:40Z-
dc.date.issued2024-07-
dc.identifier.citationBrain and Behavior, 14(7), p. 1-12en
dc.identifier.issn2162-3279en
dc.identifier.urihttps://hdl.handle.net/1959.11/64369-
dc.description.abstract<p><b>Purpose:</b> Mild cognitive impairment (MCI) can be the prodromal phase of Alzheimer's disease (AD) where appropriate intervention might prevent or delay conversion to AD. Given this, there has been increasing interest in using magnetic resonance imaging(MRI) and neuropsychological testing to predict conversion from MCI to AD. Recent evidence suggests that the choroid plexus (ChP), neural substrates implicated in brain clearance, undergo volumetric changes in MCI and AD. Whether the ChP is involved in memory changes observed in MCI and can be used to predict conversion from MCI toAD has not been explored.</p> <p><b>Method:</b> The current study used data from the Alzheimer’s Disease NeuroimagingInitiative (ADNI) database to investigate whether later progression from MCI to AD(progressive MCI [pMCI], <i>n</i> = 115) or stable MCI (sMCI, <i>n</i> = 338) was associated with memory scores using the Rey Auditory Verbal Learning Test (RAVLT) and ChP vol-umes as calculated from MRI. Classification analyses identifying pMCI or sMCI group membership were performed to compare the predictive ability of the RAVLT and ChPvolumes.</p> <p><b>Finding:</b> The results indicated a significant difference between pMCI and sMCI groups for right ChP volume, with the pMCI group showing significantly larger right ChP vol-ume (<i>p</i> = .01, 95% confidence interval [−.116, −.015]). A significant linear relationship between the RAVLT scores and right ChP volume was found across all participants, but not for the two groups separately. Classification analyses showed that a combination of left ChP volume and auditory verbal learning scores resulted in the most accurate classification performance, with group membership accurately predicted for 72% of the testing data.</p> <p><b>Conclusion:</b> These results suggest that volumetric ChP changes appear to occur before the onset of AD and might provide value in predicting conversion from MCI to AD.</p>en
dc.languageenen
dc.publisherJohn Wiley & Sons Ltden
dc.relation.ispartofBrain and Behavioren
dc.rightsAttribution 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.titleChoroid plexus volumes and auditory verbal learning scores are associated with conversion from mild cognitive impairment to Alzheimer's diseaseen
dc.typeJournal Articleen
dc.identifier.doi10.1002/brb3.3611en
dcterms.accessRightsUNE Greenen
local.contributor.firstnameMichael Jen
local.contributor.firstnameRuthen
local.contributor.firstnameRebecca Jen
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.startpage1en
local.format.endpage12en
local.peerreviewedYesen
local.identifier.volume14en
local.identifier.issue7en
local.access.fulltextYesen
local.contributor.lastnamePearsonen
local.contributor.lastnameWagstaffen
local.contributor.lastnameWilliamsen
dc.identifier.staffune-id:rwilli90en
local.profile.orcid0000-0002-8949-1197en
local.profile.roleauthoren
local.profile.roleauthoren
local.profile.roleauthoren
local.identifier.unepublicationidune:1959.11/64369en
dc.identifier.academiclevelAcademicen
dc.identifier.academiclevelAcademicen
dc.identifier.academiclevelAcademicen
local.title.maintitleChoroid plexus volumes and auditory verbal learning scores are associated with conversion from mild cognitive impairment to Alzheimer's diseaseen
local.relation.fundingsourcenoteThe Alzheimer’s Disease Neuroimaging Initiative (ADNI) (National Institutes of Health Grant U01 AG024904) and DOD ADNI (Department of Defense award number W81XWH-12-2-0012). ADNI is funded by the National Institute on Aging, the National Institute of Biomedical Imaging and Bioengineering, and through generous contributions from the following: AbbVie, Alzheimer’s Association; Alzheimer’sDrug Discovery Foundation; Araclon Biotech; BioClinica, Inc.; Biogen;B ristol-Myers Squibb Company; CereSpir, Inc.; Cogstate; Eisai Inc.; ElanPharmaceuticals, Inc.; Eli Lilly and Company; EuroImmun; F. Hoffmann-La Roche Ltd and its affiliated company Genentech, Inc.; Fujirebio; GEHealthcare; IXICO Ltd.; Janssen Alzheimer Immunotherapy Research& Development, LLC.; Johnson & Johnson Pharmaceutical Research& Development LLC.; Lumosity; Lundbeck; Merck & Co., Inc.; MesoScale Diagnostics, LLC.; NeuroRx Research; Neurotrack Technologies; Novartis Pharmaceuticals Corporation; Pfizer Inc.; Piramal Imaging; Servier; Takeda Pharmaceutical Company; and Transition Therapeutics. The Canadian Institutes of Health Research is providing funds to support ADNI clinical sites in Canada.en
local.output.categorydescriptionC1 Refereed Article in a Scholarly Journalen
local.search.authorPearson, Michael Jen
local.search.authorWagstaff, Ruthen
local.search.authorWilliams, Rebecca Jen
local.open.fileurlhttps://rune.une.edu.au/web/retrieve/546f72c7-1645-4d2c-8dbb-a887a94cfb83en
local.uneassociationNoen
dc.date.presented2024-07-
local.atsiresearchNoen
local.sensitive.culturalNoen
local.year.published2024en
local.year.presented2024en
local.fileurl.openhttps://rune.une.edu.au/web/retrieve/546f72c7-1645-4d2c-8dbb-a887a94cfb83en
local.fileurl.openpublishedhttps://rune.une.edu.au/web/retrieve/546f72c7-1645-4d2c-8dbb-a887a94cfb83en
local.subject.for20203209 Neurosciencesen
local.profile.affiliationtypeExternal Affiliationen
local.profile.affiliationtypeExternal Affiliationen
local.profile.affiliationtypeExternal Affiliationen
local.date.moved2025-01-08en
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School of Science and Technology
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