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The Ankle-Brachial Index Is Associated with Cerebral beta-Amyloid Deposition in Cognitively Normal Older Adults

Authors
Moon, Seok WooByun, Min SooYi, DahyunLee, Jun HoJeon, So YeonLee, YounghwaKee, Baik SeokLee, Dong Young
Issue Date
Jul-2019
Publisher
OXFORD UNIV PRESS INC
Keywords
Alzheimer's disease; cerebral A beta deposition; cerebral glucose metabolism; apolipoprotein E epsilon 4
Citation
JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES, v.74, no.7, pp 1141 - 1148
Pages
8
Journal Title
JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES
Volume
74
Number
7
Start Page
1141
End Page
1148
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/45114
DOI
10.1093/gerona/gly157
ISSN
1079-5006
1758-535X
Abstract
Background: Although ankle-brachial index (ABI), an indicator of atherosclerosis or arterial stiffness, has been associated with dementia and Alzheimer's disease (AD), no information is yet available for its contribution to AD pathologies. We investigated the relationship between the ABI and in vivo beta-amyloid (A) deposition and AD-specific neurodegeneration in cognitively normal (CN) elderly individuals. Methods: A total of 256 CN elderly subjects who participated in the Korean Brain Aging Study for the Early Diagnosis and Prediction of Alzheimer's Disease (KBASE), an ongoing prospective cohort study, were included. All subjects underwent comprehensive clinical and neuropsychological assessments, ABI measurement, apolipoprotein E (APOE) genotyping, [C-11]Pittsburgh Compound B (PiB)-positron emission tomography (PEI), [F-18]-fludeoxyglucose PET, and magnetic resonance imaging. Results: A significant positive association was found between the ABI and global cerebral A beta retention measured by PiB-PET, even after controlling for age, sex, and APOE epsilon 4. When three stratified ABI subgroups (ABI < 1.00, 1.00-1.29, and >= 1.30) were compared, the highest ABI subgroup (ie, ABI >= 1.30) showed significantly higher A beta deposition than that of the other subgroups. This relationship between A beta deposition and the ABI was significant only in APOE epsilon 4 carriers, but not in noncarriers. No significant association was observed between the ABI and neurodegeneration in the AD-signature regions. Conclusion: Our findings suggest that a high ABI, possibly related to arterial stiffness, is associated with elevated brain A beta burden in cognitively healthy elderly individuals, particularly in APOE epsilon 4 carriers.
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