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Amyloid burden, cerebrovascular disease, brain atrophy, and cognition in cognitively impaired patients

Authors
Ye, Byoung SeokSeo, Sang WonKim, Geon HaNoh, YoungCho, HannaYoon, Cindy W.Kim, Hee JinChin, JuheeJeong, SeunLee, Jong MinSeong, Joon-KyungKim, Jae SeungLee, Jae-HongChoe, Yearn SeongLee, Kyung HanSohn, Young H.Ewers, MichaelWeiner, MichaelNa, Duk L.
Issue Date
5월-2015
Publisher
ELSEVIER SCIENCE INC
Keywords
Cognition; Amyloid; Pittsburgh compound B; Atrophy; Cortical thickness; Hippocampus; Path analysis; Cerebrovascular disease
Citation
ALZHEIMERS & DEMENTIA, v.11, no.5, pp.494 - 503
Indexed
SCIE
SCOPUS
Journal Title
ALZHEIMERS & DEMENTIA
Volume
11
Number
5
Start Page
494
End Page
503
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/93658
DOI
10.1016/j.jalz.2014.04.521
ISSN
1552-5260
Abstract
Background: We investigated the independent effects of Alzheimer's disease (AD) and cerebrovascular disease (CVD) pathologies on brain structural changes and cognition. Methods: Amyloid burden (Pittsburgh compound B [PiB] retention ratio), CVD markers (volume of white matter hyperintensities [WMH] and number of lacunae), and structural changes (cortical thickness and hippocampal shape) were measured in 251 cognitively impaired patients. Path analyses were utilized to assess the effects of these markers on cognition. Results: PiB retention ratio was associated with hippocampal atrophy, which was associated with memory impairment. WMH were associated with frontal thinning, which was associated with executive and memory dysfunctions. PiB retention ratio and lacunae were also associated with memory and executive dysfunction without the mediation of hippocampal or frontal atrophy. Conclusions: Our results suggest that the impacts of AD and CVD pathologies on cognition are mediated by specific brain regions. (C) 2015 The Alzheimer's Association. Published by Elsevier Inc. All rights reserved.
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