Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/12242
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dc.contributor.authorBrodtmann, Amyen
dc.contributor.authorWerden, Emilioen
dc.contributor.authorPardoe, Heath Ren
dc.contributor.authorLi, Qien
dc.contributor.authorJackson, Graeme Den
dc.contributor.authorDonnan, Geoffrey Aen
dc.contributor.authorCowie, Tiffanyen
dc.contributor.authorBradshaw, Jenniferen
dc.contributor.authorDarby, David Gen
dc.contributor.authorCumming, Toby Ben
dc.date.accessioned2015-05-16T01:54:03Z
dc.date.available2015-05-16T01:54:03Z
dc.date.issued2014-06-03en
dc.identifier.citationInternational Journal of Stroke 2014; 9(6): 824-8en
dc.identifier.govdoc24894387en
dc.identifier.otherPUBMEDen
dc.identifier.urihttp://ahro.austin.org.au/austinjspui/handle/1/12242en
dc.description.abstractGlobally, stroke and dementia are leading causes of disability and mortality. More than one third of stroke patients will develop dementia, but mechanisms are unclear.The study aims to establish whether brain volume change is associated with poststroke dementia, and to elucidate potential causal mechanisms, including genetic markers, amyloid deposition and vascular risk factors. An understanding of whether - and in whom - stroke is neurodegenerative is critical for the strategic use of potential disease-modifying therapies.That stroke patients will exhibit greater brain volume loss than comparable cohorts of stroke-free controls; and that those who develop dementia will exhibit greater brain volume loss than those who do not.Advanced brain imaging techniques are used to longitudinally measure brain volume and cortical thickness in 135 stroke patients. Concurrent neuropsychological testing will correlate clinical profile with these measures.Primary imaging end-point is brain volume change between three-months and three-years poststroke; primary clinical outcome is the presence of dementia at three-years.We will examine the correlations with the following variables: dementia subtype; physical activity levels; behavioral dysfunction as measured by patient and caregiver-reported scales; structural and functional brain connectivity disruption; apolipoprotein E; and specific neuropsychological test scores.Magnetic resonance imaging markers of structural brain aging and performance on neuropsychological tests are powerful predictors of dementia. We need to understand the trajectory of regional brain volume change and cognitive decline in patients after stroke. This will allow future risk stratification for prognostic counseling, service planning, and early therapeutic intervention.en
dc.language.isoenen
dc.subject.otherMRIen
dc.subject.othercognitionen
dc.subject.othercortical thicknessen
dc.subject.otherdementiaen
dc.subject.otherhippocampusen
dc.subject.otherstrokeen
dc.subject.otherApolipoproteins E.metabolismen
dc.subject.otherBrain.pathologyen
dc.subject.otherBrain Ischemia.complications.diagnosis.pathology.psychologyen
dc.subject.otherClinical Protocolsen
dc.subject.otherCognitionen
dc.subject.otherCohort Studiesen
dc.subject.otherDementia.diagnosis.etiology.pathology.therapyen
dc.subject.otherHumansen
dc.subject.otherLongitudinal Studiesen
dc.subject.otherMagnetic Resonance Imagingen
dc.subject.otherMotor Activityen
dc.subject.otherNeuropsychological Testsen
dc.subject.otherOrgan Sizeen
dc.subject.otherPatient Selectionen
dc.subject.otherPrognosisen
dc.subject.otherSample Sizeen
dc.subject.otherStroke.complications.diagnosis.pathology.psychologyen
dc.subject.otherTime Factorsen
dc.titleCharting cognitive and volumetric trajectories after stroke: protocol for the Cognition And Neocortical Volume After Stroke (CANVAS) study.en
dc.typeJournal Articleen
dc.identifier.journaltitleInternational Journal of Strokeen
dc.identifier.affiliationEastern Clinical Research Unit, Monash University, Box Hill Hospital, Melbourne, Victoria, Australiaen
dc.identifier.affiliationAustin Health, Heidelberg, Melbourne, Victoria, Australiaen
dc.identifier.affiliationThe Florey Institute for Neuroscience and Mental Health, University of Melbourne, Melbourne, Victoria, Australiaen
dc.identifier.doi10.1111/ijs.12301en
dc.description.pages824-8en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/24894387en
dc.type.austinJournal Articleen
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