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Low Plasma ApoE Levels Are Associated with Smaller Hippocampal Size in the Alzheimer's Disease Neuroimaging Initiative Cohort
Author(s) -
Edmond Teng,
Nicole Chow,
Kristy Hwang,
Paul M. Thompson,
Karen H. Gylys,
Gregory M. Cole,
Clifford R. Jack,
Leslie M. Shaw,
John Q. Trojanowski,
Holly Soares,
Michael W. Weiner,
Liana G. Apostolova
Publication year - 2014
Publication title -
dementia and geriatric cognitive disorders
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.026
H-Index - 110
eISSN - 1421-9824
pISSN - 1420-8008
DOI - 10.1159/000368982
Subject(s) - apolipoprotein e , neuropathology , alzheimer's disease neuroimaging initiative , hippocampal formation , alzheimer's disease , psychology , hippocampus , neuroimaging , medicine , pittsburgh compound b , neuroscience , disease
Apolipoprotein E (APOE) genotype is the strongest known genetic risk factor for sporadic Alzheimer's disease (AD), but the utility of plasma ApoE levels for assessing the severity of underlying neurodegenerative changes remains uncertain. Here, we examined cross-sectional associations between plasma ApoE levels and volumetric magnetic resonance imaging indices of the hippocampus from 541 participants [57 with normal cognition (NC), 375 with mild cognitive impairment (MCI), and 109 with mild AD] who were enrolled in the Alzheimer's Disease Neuroimaging Initiative. Across the NC and MCI groups, lower plasma ApoE levels were significantly correlated with smaller hippocampal size, as measured by either hippocampal volume or hippocampal radial distance. These associations were driven primarily by findings from carriers of an APOE ε4 allele and are consistent with prior reports that lower plasma ApoE levels correlate with greater global cortical Pittsburgh Compound B retention. In this high-risk group, plasma ApoE levels may represent a peripheral marker of underlying AD neuropathology in nondemented elderly individuals.

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