Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/11434
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dc.contributor.authorChételat, G-
dc.contributor.authorVillemagne, Victor L-
dc.contributor.authorVillain, N-
dc.contributor.authorJones, G-
dc.contributor.authorEllis, Kathryn A-
dc.contributor.authorAmes, David-
dc.contributor.authorMartins, Ralph N-
dc.contributor.authorMasters, Colin L-
dc.contributor.authorRowe, Christopher C-
dc.date.accessioned2015-05-16T01:02:37Z
dc.date.available2015-05-16T01:02:37Z
dc.date.issued2012-02-01-
dc.identifier.citationNeurology 2012; 78(7): 477-84en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/11434en
dc.description.abstractGiven the recent and growing interest in the concepts of prodromal and presymptomatic Alzheimer disease, it is crucial to determine whether the presence of β-amyloid (Aβ) in the brain of asymptomatic elderly individuals is a pathologic condition associated with accelerated neuronal and synaptic loss. The aim of the present study was to assess whether Aβ influences the rate of atrophy in cognitively normal elderly individuals.Seventy-four healthy elderly individuals underwent an MRI scan and a 11C-Pittsburgh compound B (PiB) PET scan at baseline and a second MRI scan 18 months later. Voxel-wise analyses were performed using maps of annual rate of atrophy generated from the serial MRI scans, including comparison between individuals with high vs low neocortical PiB and correlation with baseline neocortical PiB.The rate of atrophy was significantly higher in the normal elderly individuals with high PiB compared with those with low PiB and was significantly correlated with baseline neocortical PiB, with the highest significance in the temporal neocortex and the posterior cingulate cortex.Our findings show that the presence of Aβ in the brain, known to occur in about one-third of asymptomatic elderly individuals, is actually a pathologic state associated with accelerated atrophy. They also suggest that therapy aimed to reduce the neurodegenerative process should be commenced in presymptomatic individuals with high PiB.en
dc.language.isoenen
dc.subject.otherAgeden
dc.subject.otherAged, 80 and overen
dc.subject.otherAmyloid beta-Peptides.metabolismen
dc.subject.otherAniline Compounds.diagnostic useen
dc.subject.otherAtrophyen
dc.subject.otherBrain Mappingen
dc.subject.otherCerebellum.pathologyen
dc.subject.otherCerebral Cortex.pathology.radionuclide imagingen
dc.subject.otherCognition.physiologyen
dc.subject.otherDisease Progressionen
dc.subject.otherFemaleen
dc.subject.otherHumansen
dc.subject.otherImage Processing, Computer-Assisteden
dc.subject.otherMagnetic Resonance Imagingen
dc.subject.otherMaleen
dc.subject.otherMild Cognitive Impairment.pathology.psychologyen
dc.subject.otherNeocortex.pathologyen
dc.subject.otherPositron-Emission Tomographyen
dc.subject.otherRadiopharmaceuticals.diagnostic useen
dc.subject.otherThiazoles.diagnostic useen
dc.titleAccelerated cortical atrophy in cognitively normal elderly with high β-amyloid deposition.en
dc.typeJournal Articleen
dc.identifier.journaltitleNeurologyen
dc.identifier.affiliationchetelat@cyceron.fren
dc.identifier.affiliationDepartment of Nuclear Medicine, Austin Health, Melbourne, Australiaen
dc.identifier.doi10.1212/WNL.0b013e318246d67aen
dc.description.pages477-84en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/22302548en
dc.contributor.corpauthorAIBL Research Groupen
dc.type.contentTexten
dc.type.austinJournal Articleen
local.name.researcherMasters, Colin L
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
crisitem.author.deptMolecular Imaging and Therapy-
crisitem.author.deptThe Florey Institute of Neuroscience and Mental Health-
crisitem.author.deptMolecular Imaging and Therapy-
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