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In vivo cortical spreading pattern of tau and amyloid in the Alzheimer disease spectrum

DC Field Value Language
dc.contributor.author류철형-
dc.contributor.author유영훈-
dc.contributor.author이명식-
dc.contributor.author이재훈-
dc.contributor.author이혜미-
dc.contributor.author이혜선-
dc.contributor.author조한나-
dc.contributor.author최재용-
dc.date.accessioned2017-10-26T07:16:14Z-
dc.date.available2017-10-26T07:16:14Z-
dc.date.issued2016-
dc.identifier.issn0364-5134-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/151818-
dc.description.abstractOBJECTIVE: To determine the in vivo cortical spreading pattern of tau and amyloid and to establish positron emission tomography (PET) image-based tau staging in the Alzheimer disease (AD) spectrum. METHODS: We included 195 participants (53 AD, 52 amnestic mild cognitive impairment [MCI], 23 nonamnestic MCI, and 67 healthy controls) who underwent 2 PET scans ((18) F-florbetaben for amyloid-β and (18) F-AV-1451 for tau). We assumed that regions with earlier appearances of pathology may show increased binding in a greater number of participants and acquired spreading order of tau accumulation by sorting the regional frequencies of involvement. We classified each participant into image-based tau stage based on the Z score of the composite region for each stage. RESULTS: Tau accumulation was most frequently observed in the medial temporal regions and spread stepwise to the basal and lateral temporal, inferior parietal, posterior cingulate, and other association cortices, and then ultimately to the primary cortical regions. In contrast, amyloid accumulation was found with similar frequency in the diffuse neocortical areas and then finally spread to the medial temporal regions. The image-based tau stage correlated with the general cognitive status, whereas cortical thinning was found only in the advanced tau stages: medial temporal region in stage V and widespread cortex in stage VI. INTERPRETATION: Our PET study replicated postmortem spreading patterns of tau and amyloid-β pathologies. Unlike the diffuse accumulation of amyloid throughout the neocortex, tau spreading occurred in a stepwise fashion through the networks. Image-based tau staging may be useful for the objective assessment of AD progression-
dc.description.statementOfResponsibilityrestriction-
dc.publisherWiley-Liss-
dc.relation.isPartOfANNALS OF NEUROLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAged-
dc.subject.MESHAlzheimer Disease/metabolism*-
dc.subject.MESHAlzheimer Disease/pathology-
dc.subject.MESHAmnesia/complications-
dc.subject.MESHAmnesia/metabolism-
dc.subject.MESHAmnesia/pathology-
dc.subject.MESHAmyloid/metabolism*-
dc.subject.MESHAtrophy/pathology-
dc.subject.MESHCerebral Cortex/metabolism*-
dc.subject.MESHCerebral Cortex/pathology-
dc.subject.MESHCognitive Dysfunction/complications-
dc.subject.MESHCognitive Dysfunction/metabolism*-
dc.subject.MESHCognitive Dysfunction/pathology-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHMagnetic Resonance Imaging-
dc.subject.MESHMale-
dc.subject.MESHNeuroimaging-
dc.subject.MESHNeuropsychological Tests-
dc.subject.MESHPositron-Emission Tomography-
dc.subject.MESHtau Proteins/metabolism*-
dc.titleIn vivo cortical spreading pattern of tau and amyloid in the Alzheimer disease spectrum-
dc.typeArticle-
dc.publisher.locationUnited States-
dc.contributor.collegeCollege of Medicine-
dc.contributor.departmentDept. of Neurology-
dc.contributor.googleauthorHanna Cho-
dc.contributor.googleauthorJae Yong Choi-
dc.contributor.googleauthorMi Song Hwang-
dc.contributor.googleauthorYou Jin Kim-
dc.contributor.googleauthorHye Mi Lee-
dc.contributor.googleauthorHye Sun Lee-
dc.contributor.googleauthorJae Hoon Lee-
dc.contributor.googleauthorYoung Hoon Ryu-
dc.contributor.googleauthorMyung Sik Lee-
dc.contributor.googleauthorChul Hyoung Lyoo-
dc.identifier.doi10.1002/ana.24711-
dc.contributor.localIdA02485-
dc.contributor.localIdA02753-
dc.contributor.localIdA03093-
dc.contributor.localIdA05019-
dc.contributor.localIdA03312-
dc.contributor.localIdA03920-
dc.contributor.localIdA04695-
dc.contributor.localIdA01333-
dc.relation.journalcodeJ00166-
dc.identifier.eissn1531-8249-
dc.identifier.pmid27323247-
dc.identifier.urlhttp://onlinelibrary.wiley.com/doi/10.1002/ana.24711/abstract-
dc.contributor.alternativeNameLyoo, Chul Hyoung-
dc.contributor.alternativeNameRyu, Young Hoon-
dc.contributor.alternativeNameLee, Myung Sik-
dc.contributor.alternativeNameLee, Jae Hoon-
dc.contributor.alternativeNameLee, Hye Mi-
dc.contributor.alternativeNameLee, Hye Sun-
dc.contributor.alternativeNameCho, Hanna-
dc.contributor.alternativeNameChoi, Jae Yong-
dc.contributor.affiliatedAuthorRyu, Young Hoon-
dc.contributor.affiliatedAuthorLee, Myung Sik-
dc.contributor.affiliatedAuthorLee, Jae Hoon-
dc.contributor.affiliatedAuthorLee, Hye Mi-
dc.contributor.affiliatedAuthorLee, Hye Sun-
dc.contributor.affiliatedAuthorCho, Hanna-
dc.contributor.affiliatedAuthorChoi, Jae Yong-
dc.contributor.affiliatedAuthorLyoo, Chul Hyoung-
dc.citation.volume80-
dc.citation.number2-
dc.citation.startPage247-
dc.citation.endPage258-
dc.identifier.bibliographicCitationANNALS OF NEUROLOGY, Vol.80(2) : 247-258, 2016-
dc.date.modified2017-10-24-
dc.identifier.rimsid45827-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Neurology (신경과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Nuclear Medicine (핵의학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Yonsei Biomedical Research Center (연세의생명연구원) > 1. Journal Papers

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