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Hippocampal and cortical atrophy in amyloid-negative mild cognitive impairments: comparison with amyloid-positive mild cognitive impairment

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dc.contributor.authorYe, Byoung Seok-
dc.contributor.authorSeo, Sang Won-
dc.contributor.authorKim, Chi Hun-
dc.contributor.authorJeon, Seun-
dc.contributor.authorKim, Geon Ha-
dc.contributor.authorNoh, Young-
dc.contributor.authorCho, Hanna-
dc.contributor.authorYoon, Cindy W.-
dc.contributor.authorKim, Hee Jin-
dc.contributor.authorJang, Eun Young-
dc.contributor.authorLee, Jeongmin-
dc.contributor.authorKim, Jung-Hyun-
dc.contributor.authorChin, Juhee-
dc.contributor.authorLee, Jong Min-
dc.contributor.authorKim, Jeong-Hun-
dc.contributor.authorSeong, Joon-kyung-
dc.contributor.authorKim, Chang-Hun-
dc.contributor.authorChoe, Yearn Seong-
dc.contributor.authorLee, Kyung Han-
dc.contributor.authorNa, Duk L.-
dc.date.available2020-02-28T18:41:56Z-
dc.date.created2020-02-06-
dc.date.issued2014-02-
dc.identifier.issn0197-4580-
dc.identifier.urihttps://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/12849-
dc.description.abstractAlthough patients with amnestic mild cognitive impairment (aMCI) are at higher risk of developing Alzheimer's disease (AD), their pathologies could be heterogeneous. We aimed to evaluate structural changes in amyloid-negative and amyloid-positive aMCI patients. Forty-eight aMCI patients who underwent Pittsburgh compound B (PiB) positron emission tomography were recruited. They were classified as PiB (-) aMCI (N = 16) and PiB (+) (N = 32). Hippocampal shape and regional cortical thickness were compared with 41 subjects with normal cognition (NC). Relative to NC, PiB(-) aMCI exhibited hippocampal deformity in the right cornu ammonis 1, whereas PiB(+) aMCI exhibited hippocampal deformity in bilateral subiculum and cornu ammonis 1 subregions. Relative to NC, PiB(-) aMCI showed cortical thinning in the left medial prefrontal and right anterior temporal regions, whereas PiB(+) aMCI exhibited cortical thinning in bilateral medial temporal regions, temporoparietal junctions and precuneus, and prefrontal cortices. Our findings suggest that structural changes in PiB(-) aMCI might be due to several possible pathologic changes, whereas structural changes in PiB(+) aMCI reflect AD-like structural changes. (C) 2014 Elsevier Inc. All rights reserved.-
dc.language영어-
dc.language.isoen-
dc.publisherELSEVIER SCIENCE INC-
dc.relation.isPartOfNEUROBIOLOGY OF AGING-
dc.subjectVOXEL-BASED MORPHOMETRY-
dc.subjectALZHEIMERS-DISEASE-
dc.subjectBLOOD-PRESSURE-
dc.subjectVASCULAR DEMENTIA-
dc.subjectSHAPE-ANALYSIS-
dc.subjectBRAIN ATROPHY-
dc.subjectTEMPORAL-LOBE-
dc.subjectCOMPOUND-B-
dc.subjectDEPRESSION-
dc.subjectPATTERNS-
dc.titleHippocampal and cortical atrophy in amyloid-negative mild cognitive impairments: comparison with amyloid-positive mild cognitive impairment-
dc.typeArticle-
dc.type.rimsART-
dc.description.journalClass1-
dc.identifier.wosid000328655600003-
dc.identifier.doi10.1016/j.neurobiolaging.2013.08.017-
dc.identifier.bibliographicCitationNEUROBIOLOGY OF AGING, v.35, no.2, pp.291 - 300-
dc.identifier.scopusid2-s2.0-84887232865-
dc.citation.endPage300-
dc.citation.startPage291-
dc.citation.titleNEUROBIOLOGY OF AGING-
dc.citation.volume35-
dc.citation.number2-
dc.contributor.affiliatedAuthorNoh, Young-
dc.type.docTypeArticle-
dc.subject.keywordAuthorMild cognitive impairment-
dc.subject.keywordAuthorAlzheimer&apos-
dc.subject.keywordAuthors disease-
dc.subject.keywordAuthorPittsburgh compound B-
dc.subject.keywordAuthorCortical thickness-
dc.subject.keywordAuthorHippocampus-
dc.subject.keywordPlusVOXEL-BASED MORPHOMETRY-
dc.subject.keywordPlusALZHEIMERS-DISEASE-
dc.subject.keywordPlusBLOOD-PRESSURE-
dc.subject.keywordPlusVASCULAR DEMENTIA-
dc.subject.keywordPlusSHAPE-ANALYSIS-
dc.subject.keywordPlusBRAIN ATROPHY-
dc.subject.keywordPlusTEMPORAL-LOBE-
dc.subject.keywordPlusCOMPOUND-B-
dc.subject.keywordPlusDEPRESSION-
dc.subject.keywordPlusPATTERNS-
dc.relation.journalResearchAreaGeriatrics & Gerontology-
dc.relation.journalResearchAreaNeurosciences & Neurology-
dc.relation.journalWebOfScienceCategoryGeriatrics & Gerontology-
dc.relation.journalWebOfScienceCategoryNeurosciences-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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