Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/23073
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dc.contributor.authorJeong, Hye Jin-
dc.contributor.authorLee, Hyon-
dc.contributor.authorLee, Sang Yoon-
dc.contributor.authorSeo, Seongho-
dc.contributor.authorPark, Kee Hyung-
dc.contributor.authorLee, Yeong Bae-
dc.contributor.authorShin, Dong Jin-
dc.contributor.authorKang, Jae Myeong-
dc.contributor.authorYeon, Byeong Kil-
dc.contributor.authorKang, Seung Gul-
dc.contributor.authorCho, Jaelim-
dc.contributor.authorSeong, Joon Kyung-
dc.contributor.authorOkamura, Nobuyuki-
dc.contributor.authorVillemagne, Victor L-
dc.contributor.authorNa, Duk L-
dc.contributor.authorNoh, Young-
dc.date.accessioned2020-04-28T23:20:03Z-
dc.date.available2020-04-28T23:20:03Z-
dc.date.issued2020-04-
dc.identifier.citationJournal of clinical neurology (Seoul, Korea) 2020; 16(2): 202-214en
dc.identifier.issn1738-6586-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/23073-
dc.description.abstractMild cognitive impairment (MCI) is a condition with diverse clinical outcomes and subgroups. Here we investigated the topographic distribution of tau in vivo using the positron emission tomography (PET) tracer [¹⁸F]THK5351 in MCI subgroups. This study included 96 participants comprising 38 with amnestic MCI (aMCI), 21 with nonamnestic MCI (naMCI), and 37 with normal cognition (NC) who underwent 3.0-T MRI, [¹⁸F]THK5351 PET, and detailed neuropsychological tests. [¹⁸F]flutemetamol PET was also performed in 62 participants. The aMCI patients were further divided into three groups: 1) verbal-aMCI, only verbal memory impairment; 2) visual-aMCI, only visual memory impairment; and 3) both-aMCI, both visual and verbal memory impairment. Voxel-wise statistical analysis and region-of-interest -based analyses were performed to evaluate the retention of [¹⁸F]THK5351 in the MCI subgroups. Subgroup analysis of amyloid-positive and -negative MCI patients was also performed. Correlations between [¹⁸F]THK5351 retention and different neuropsychological tests were evaluated using statistical parametric mapping analyses. [¹⁸F]THK5351 retention in the lateral temporal, mesial temporal, parietal, frontal, posterior cingulate cortices and precuneus was significantly greater in aMCI patients than in NC subjects, whereas it did not differ significantly between naMCI and NC participants. [¹⁸F] THK5351 retention was greater in the both-aMCI group than in the verbal-aMCI and visualaMCI groups, and greater in amyloid-positive than amyloid-negative MCI patients. The cognitive function scores were significantly correlated with cortical [¹⁸F]THK5351 retention. [¹⁸F]THK5351 PET might be useful for identifying distinct topographic patterns of [¹⁸F]THK5351 retention in subgroups of MCI patients who are at greater risk of the progression to Alzheimer's dementia.en
dc.language.isoeng-
dc.subjectmild cognitive impairmenten
dc.subjectneurofibrillary tanglesen
dc.subjectpositron emission tomographyen
dc.title[¹⁸F]THK5351 PET Imaging in Patients with Mild Cognitive Impairment.en
dc.typeJournal Articleen
dc.identifier.journaltitleJournal of clinical neurology (Seoul, Korea)en
dc.identifier.affiliationDepartment of Health Science and Technology, GAIHST, Gachon University, Incheon, Koreaen
dc.identifier.affiliationDepartment of Molecular Imaging and Therapy, Austin Health, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationDepartment of Neurology, Gachon University Gil Medical Center, Incheon, Koreaen
dc.identifier.affiliationCentre for PET, Austin Health, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationDepartment of Neurology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Koreaen
dc.identifier.affiliationDepartment of Biomedical Engineering, Korea University, Seoul, Koreaen
dc.identifier.affiliationDepartment of Medicine, The University of Melbourne, Melbourne, VIC, Australiaen
dc.identifier.affiliationDepartment of Neuroscience, College of Medicine, Gachon University, Incheon, Koreaen
dc.identifier.affiliationNeuroscience Research Institute, Gachon University, Incheon, Koreaen
dc.identifier.affiliationDepartment of Occupational and Environmental Medicine, Gachon University Gil Medical Center, Incheon, Koreaen
dc.identifier.affiliationDepartment of Psychiatry, Gachon University Gil Medical Center, Incheon, Koreaen
dc.identifier.affiliationDepartment of Artificial Intelligence, Korea University, Seoul, Koreaen
dc.identifier.affiliationSamsung Alzheimer Research Center, Samsung Medical Center, Seoul, Koreaen
dc.identifier.affiliationTohoku Medical and Pharmaceutical University, Sendai, Japanen
dc.identifier.doi10.3988/jcn.2020.16.2.202en
dc.type.contentTexten
dc.identifier.orcid0000-0003-3765-8546en
dc.identifier.orcid0000-0002-0273-8960en
dc.identifier.orcid0000-0002-6029-8553en
dc.identifier.orcid0000-0001-7894-0535en
dc.identifier.orcid0000-0001-6847-6679en
dc.identifier.orcid0000-0001-5952-1423en
dc.identifier.orcid0000-0002-4390-2843en
dc.identifier.orcid0000-0003-0803-9332en
dc.identifier.orcid0000-0002-4853-3178en
dc.identifier.orcid0000-0003-4933-0433en
dc.identifier.orcid0000-0002-4524-0310en
dc.identifier.orcid0000-0001-6291-5415en
dc.identifier.orcid0000-0002-5991-7812en
dc.identifier.orcid0000-0002-5832-9875en
dc.identifier.orcid0000-0003-1572-7862en
dc.identifier.orcid0000-0002-9633-3314en
dc.identifier.pubmedid32319236-
dc.type.austinJournal Article-
local.name.researcherVillemagne, Victor 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-
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