Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/30564
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dc.contributor.authorKrishnadas, Natasha-
dc.contributor.authorHuang, Kun-
dc.contributor.authorSchultz, Stephanie A-
dc.contributor.authorDoré, Vincent-
dc.contributor.authorBourgeat, Pierrick-
dc.contributor.authorGoh, Anita M Y-
dc.contributor.authorLamb, Fiona-
dc.contributor.authorBozinovski, Svetlana-
dc.contributor.authorBurnham, Samantha C-
dc.contributor.authorRobertson, Joanne S-
dc.contributor.authorLaws, Simon M-
dc.contributor.authorMaruff, Paul-
dc.contributor.authorMasters, Colin L-
dc.contributor.authorVillemagne, Victor L-
dc.contributor.authorRowe, Christopher C-
dc.date2022-
dc.date.accessioned2022-07-19T06:58:08Z-
dc.date.available2022-07-19T06:58:08Z-
dc.date.issued2022-07-07-
dc.identifier.citationJournal of Alzheimer's Disease: JAD 2022; 88(4): 1627-1637en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/30564-
dc.description.abstractIn Alzheimer's disease, heterogeneity has been observed in the postmortem distribution of tau neurofibrillary tangles. Visualizing the topography of tau in vivo may facilitate clinical trials and clinical practice. This study aimed to investigate whether tau distribution patterns that are limited to mesial temporal lobe (MTL)/limbic regions, and those that spare MTL regions, can be visually identified using 18F-MK6240, and whether these patterns are associated with different demographic and cognitive profiles. Tau 18F-MK6240 PET images of 151 amyloid-β positive participants with mild cognitive impairment (MCI) and dementia were visually rated as: tau negative, limbic predominant (LP), MTL-sparing, and Typical by two readers. Groups were evaluated for differences in age, APOE ɛ4 carriage, hippocampal volumes, and cognition (MMSE, composite memory and non-memory scores). Voxel-wise contrasts were also performed. Visual rating resulted in 59.6% classified as Typical, 17.9% as MTL-sparing, 9.9% LP, and 12.6% as tau negative. Intra-rater and inter-rater reliability was strong (Cohen's kappa values of 0.89 and 0.86 respectively). Tracer retention in a "hook"-like distribution on sagittal sequences was observed in the LP and Typical groups. The visually classified MTL-sparing group had lower APOE ɛ4 carriage and relatively preserved hippocampal volumes. Higher MTL tau was associated with greater amnestic cognitive impairment. High cortical tau was associated with greater impairments on non-memory domains of cognition, and individuals with high cortical tau were more likely to have dementia than MCI. Tau distribution patterns can be visually identified using 18F-MK6240 PET and are associated with differences in APOE ɛ4 carriage, hippocampal volumes, and cognition.en
dc.language.isoeng-
dc.subject18F-MK6240en
dc.subjectAlzheimer’s diseaseen
dc.subjectcognitionen
dc.subjectpatternsen
dc.subjectpositron emission tomographyen
dc.subjecttauen
dc.titleVisually Identified Tau 18F-MK6240 PET Patterns in Symptomatic Alzheimer's Disease.en
dc.typeJournal Articleen
dc.identifier.journaltitleJournal of Alzheimer's disease : JADen
dc.identifier.affiliationFlorey Department of Neurosciences & Mental Health, The University of Melbourne, Parkville, VIC, Australia..en
dc.identifier.affiliationMolecular Imaging and Therapyen
dc.identifier.affiliationNational Ageing Research Institute, Parkville, VIC, Australia..en
dc.identifier.affiliationHealth and Biosecurity Flagship, The Australian eHealth Research Centre, Melbourne, Victoria, Australia..en
dc.identifier.affiliationHealth and Biosecurity Flagship, The Australian eHealth Research Centre, Brisbane, QLD, Australia..en
dc.identifier.affiliationDepartment of Psychiatry, The University of Melbourne, Parkville, VIC, Australia..en
dc.identifier.affiliationCollaborative Genomics and Translation Group, School of Medical and Health Sciences, Edith Cowan University, Perth, WA, Australia..en
dc.identifier.affiliationThe Florey Institute of Neuroscience and Mental Healthen
dc.identifier.affiliationCentre for Precision Health, Edith Cowan University, Perth, WA, Australia..en
dc.identifier.affiliationDepartment of Psychiatry, University of Pittsburgh, Pittsburgh, PA, USA..en
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/35811517/en
dc.identifier.doi10.3233/JAD-215558en
dc.type.contentTexten
dc.identifier.orcid0000-0002-5374-2839en
dc.identifier.orcid0000-0001-8460-4415en
dc.identifier.orcid0000-0002-8051-0558en
dc.identifier.orcid0000-0001-6533-8641en
dc.identifier.orcid0000-0002-6947-9537en
dc.identifier.orcid0000-0003-3072-7940en
dc.identifier.orcid0000-0002-5832-9875en
dc.identifier.orcid0000-0003-3910-2453en
dc.identifier.pubmedid35811517-
local.name.researcherBozinovski, Svetlana
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.deptMolecular Imaging and Therapy-
crisitem.author.deptMolecular Imaging and Therapy-
crisitem.author.deptMolecular Imaging and Therapy-
crisitem.author.deptMolecular Imaging and Therapy-
crisitem.author.deptMolecular Imaging and Therapy-
crisitem.author.deptThe Florey Institute of Neuroscience and Mental Health-
crisitem.author.deptMolecular Imaging and Therapy-
crisitem.author.deptMolecular Imaging and Therapy-
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