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Effects of cerebrovascular disease and amyloid beta burden on cognition in subjects with subcortical vascular cognitive impairment.

Authors :
Park, Jae-Hyun
Seo, Sang Won
Kim, Changsoo
Kim, Sook Hui
Kim, Geon Ha
Kim, Sung Tae
Jeon, Seun
Lee, Jong Min
Oh, Seung Jun
Kim, Jae Seung
Choe, Yearn Seong
Lee, Kyung-Han
Shin, Ji Soo
Kim, Chi Hun
Noh, Young
Cho, Hanna
Yoon, Cindy W.
Kim, Hee Jin
Ye, Byoung Seok
Ewers, Michael
Source :
Neurobiology of Aging. Jan2014, Vol. 35 Issue 1, p254-260. 7p.
Publication Year :
2014

Abstract

Abstract: Cerebrovascular disease (CVD) and amyloid burden are the most frequent pathologies in subjects with cognitive impairment. However, the relationship between CVD, amyloid burden, and cognition are largely unknown. We aimed to evaluate whether CVD (lacunes, white matter hyperintensities, and microbleeds) and amyloid burden (Pittsburgh compound B [PiB] retention ratio) contribute to cognitive impairment independently or interactively. We recruited 136 patients with subcortical vascular cognitive impairment who underwent magnetic resonance imaging, PiB–positron emission tomography, and neuropsychological testing. The number of lacunes was associated with memory, frontal dysfunctions, and disease severity. The volume of white matter hyperintensities and the PiB retention ratio were associated only with memory dysfunction. There was no direct correlation between CVD markers and PiB retention ratio except that the number of lacunes was negatively correlated with the PiB retention ratio. In addition, there were no interactive effects of CVD and PiB retention ratio on cognition. Our findings suggest that CVD and amyloid burden contribute independently and not interactively to specific patterns of cognitive dysfunction in patients with subcortical vascular cognitive impairment. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
01974580
Volume :
35
Issue :
1
Database :
Academic Search Index
Journal :
Neurobiology of Aging
Publication Type :
Academic Journal
Accession number :
90627474
Full Text :
https://doi.org/10.1016/j.neurobiolaging.2013.06.026