Ye, Byoung Seok; Seo, Sang Won; Kim, Geon Ha; Noh, Young; Cho, Hanna; Yoon, Cindy W; Kim, Hee Jin; Chin, Juhee; Jeon, Seun; Lee, Jong Min; Seong, Joon-Kyung; Kim, Jae Seung; Lee, Jae-Hong; Choe, Yearn Seong; Lee, Kyung Han; Sohn, Young H; Ewers, Michael; Weiner, Michael; Na, Duk L

doi:10.1016/j.jalz.2014.04.521

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

Published Web Location

https://doi.org/10.1016/j.jalz.2014.04.521

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.

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