Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/25734
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dc.contributor.authorTaswell, Carl-
dc.contributor.authorVillemagne, Victor L-
dc.contributor.authorYates, Paul A-
dc.contributor.authorShimada, Hitoshi-
dc.contributor.authorLeyton, Cristian E-
dc.contributor.authorBallard, Kirrie J-
dc.contributor.authorPiguet, Olivier-
dc.contributor.authorBurrell, James R-
dc.contributor.authorHodges, John R-
dc.contributor.authorRowe, Christopher C-
dc.date2015-08-06-
dc.date.accessioned2021-02-01T03:58:01Z-
dc.date.available2021-02-01T03:58:01Z-
dc.date.issued2015-10-
dc.identifier.citationJournal of Nuclear Medicine 2015; 56(10): 1547-53en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/25734-
dc.description.abstractAlzheimer disease is the cause of up to one-third of cases of primary progressive aphasia or corticobasal syndrome. The primary objective of this study was to determine the accuracy of 18F-FDG PET metabolic imaging for the detection of Alzheimer disease in patients with primary progressive aphasia or corticobasal syndrome. A cohort of patients (n=94), including those with an expert clinical diagnosis of logopenic (n=19), nonfluent (n=16), or semantic (n=13) variants of primary progressive aphasia, corticobasal syndrome (n=14), or Alzheimer disease (n=24), underwent 18F-FDG metabolic and 11C-labeled Pittsburgh compound B (11C-PiB) amyloid PET brain imaging. 18F-FDG PET scans interpreted with Neurostat and 3D-SSP displays were classified as revealing Alzheimer disease or "other" by interpreters who were unaware of the clinical assessments and 11C-PiB PET results. 11C-PiB PET imaging was considered to be the diagnostic reference standard, with a threshold standardized uptake value ratio of 1.5 being indicative of Alzheimer disease pathology. To address possible bias from subgroup selection for the Alzheimer disease binary classifier, we calculated both conventional and balanced accuracies. Diagnoses of Alzheimer disease based on 18F-FDG PET resulted in 84% accuracy (both conventional and balanced). In comparison, diagnoses based on clinical assessments resulted in 65% conventional accuracy and 67% balanced accuracy. Brain 18F-FDG PET scans interpreted with Neurostat and 3D-SSP displays accurately detected Alzheimer disease in patients with primary progressive aphasia or corticobasal syndrome as focal-onset dementias. In such diagnostically challenging cohorts, (18)F-FDG PET imaging can provide more accurate diagnoses, enabling more appropriate therapy.en
dc.subject11C-PiBen
dc.subject18F-FDGen
dc.subjectAlzheimer diseaseen
dc.subjectPET brain imagingen
dc.subjectfocal-onset dementiasen
dc.title18F-FDG PET Improves Diagnosis in Patients with Focal-Onset Dementiasen
dc.typeJournal Articleen
dc.identifier.journaltitleJournal of Nuclear Medicineen
dc.identifier.affiliationDepartment of Psychiatry, University of California San Diego, San Diego, Californiaen
dc.identifier.affiliationMolecular Imaging and Therapyen
dc.identifier.affiliationNIRS Molecular Imaging Center, Chiba, Japanen
dc.identifier.affiliationUniversity of Sydney Health Sciences, Sydney, New South Wales, Australiaen
dc.identifier.affiliationARC Centre of Excellence in Cognition and Its Disorders, Neuroscience Research Australia, Sydney, New South Wales, Australiaen
dc.identifier.affiliationUniversity of New South Wales Medical Sciences, Sydney, New South Wales, Australiaen
dc.identifier.doi10.2967/jnumed.115.161067en
dc.type.contentTexten
dc.identifier.pubmedid26251415-
dc.type.austinJournal Articleen
local.name.researcherRowe, Christopher C
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.deptMolecular Imaging and Therapy-
crisitem.author.deptAged Care-
crisitem.author.deptGeriatric Medicine-
crisitem.author.deptMolecular Imaging and Therapy-
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