Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/22748
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dc.contributor.authorAmadoru, Sanka-
dc.contributor.authorDoré, Vincent-
dc.contributor.authorMcLean, Catriona A-
dc.contributor.authorHinton, Fairlie-
dc.contributor.authorShepherd, Claire E-
dc.contributor.authorHalliday, Glenda M-
dc.contributor.authorLeyton, Cristian E-
dc.contributor.authorYates, Paul A-
dc.contributor.authorHodges, John R-
dc.contributor.authorMasters, Colin L-
dc.contributor.authorVillemagne, Victor L-
dc.contributor.authorRowe, Christopher C-
dc.date2020-03-04-
dc.date.accessioned2020-03-10T22:06:20Z-
dc.date.available2020-03-10T22:06:20Z-
dc.date.issued2020-03-04-
dc.identifier.citationAlzheimer's research & therapy 2020; 12(1): 22en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/22748-
dc.description.abstractThe Centiloid scale was developed to standardise the results of beta-amyloid (Aβ) PET. We aimed to determine the Centiloid unit (CL) thresholds for CERAD sparse and moderate-density neuritic plaques, Alzheimer's disease neuropathologic change (ADNC) score of intermediate or high probability of Alzheimer's Disease (AD), final clinicopathological diagnosis of AD, and expert visual read of a positive Aβ PET scan. Aβ PET results in CL for 49 subjects were compared with post-mortem findings, visual read, and final clinicopathological diagnosis. The Youden Index was used to determine the optimal CL thresholds from receiver operator characteristic (ROC) curves. A threshold of 20.1 CL (21.3 CL when corrected for time to death, AUC 0.97) yielded highest accuracy in detecting moderate or frequent plaque density while < 10 CL was optimal for excluding neuritic plaque. The threshold for ADNC intermediate or high likelihood AD was 49.4 CL (AUC 0.98). Those cases with a final clinicopathological diagnosis of AD yielded a median CL result of 87.7 (IQR ± 42.2) with 94% > 45 CL. Positive visual read agreed highly with results > 26 CL. Centiloid values < 10 accurately reflected the absence of any neuritic plaque and > 20 CL indicated the presence of at least moderate plaque density, but approximately 50 CL or more best confirmed both neuropathological and clinicopathological diagnosis of Alzheimer's disease.en
dc.language.isoeng-
dc.subjectAlzheimer’s diseaseen
dc.subjectAmyloid imagingen
dc.subjectCentiloidsen
dc.subjectNeuropathologyen
dc.subjectPositron emission tomographyen
dc.titleComparison of amyloid PET measured in Centiloid units with neuropathological findings in Alzheimer's disease.en
dc.typeJournal Articleen
dc.identifier.journaltitleAlzheimer's research & therapyen
dc.identifier.affiliationCSIRO Health and Biosecurity, Parkville, Victoria, 3052, Australiaen
dc.identifier.affiliationDepartment of Molecular Imaging and Therapy, Austin Health, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationSydney Brain Bank, Neuroscience Research Australia and Faculty of Medicine, University of NSW, Sydney, Australiaen
dc.identifier.affiliationVictorian Brain Bank, The Florey Institute of Neuroscience and Mental Health, Melbourne, Australiaen
dc.identifier.affiliationThe Brain and Mind Centre, Faculty of Medicine and Health, University of Sydney, Sydney, Australiaen
dc.identifier.doi10.1186/s13195-020-00587-5en
dc.type.contentTexten
dc.identifier.orcid0000-0002-0522-6143en
dc.identifier.orcid0000-0002-8051-0558en
dc.identifier.orcid0000-0002-9259-8411en
dc.identifier.orcid0000-0002-0399-3218en
dc.identifier.orcid0000-0003-0422-8398en
dc.identifier.orcid0000-0002-8236-6561en
dc.identifier.orcid0000-0001-9317-0145en
dc.identifier.orcid0000-0003-3072-7940en
dc.identifier.orcid0000-0002-5832-9875en
dc.identifier.orcid0000-0003-3910-2453en
dc.identifier.pubmedid32131891-
dc.type.austinJournal Article-
local.name.researcherAmadoru, Sanka
item.grantfulltextnone-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.deptAged Care-
crisitem.author.deptMolecular Imaging and Therapy-
crisitem.author.deptAged Care-
crisitem.author.deptGeriatric Medicine-
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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