Increased hippocampal activation in ApoE-4 carriers and non-carriers with amnestic mild cognitive impairment

被引:36
作者
Tran, Tammy T. [1 ]
Speck, Caroline L. [2 ]
Pisupati, Aparna [2 ]
Gallagher, Michela [1 ]
Bakker, Arnold [2 ]
机构
[1] Johns Hopkins Univ, Sch Arts & Sci, Dept Psychol & Brain Sci, Baltimore, MD 21218 USA
[2] Johns Hopkins Univ, Sch Med, Dept Psychiat & Behav Sci, 600 N Wolfe St,Phipps 300, Baltimore, MD 21287 USA
关键词
MEDIAL TEMPORAL-LOBE; ALZHEIMERS-DISEASE; PATTERN SEPARATION; BRAIN ACTIVATION; GENETIC RISK; MEMORY; FMRI; APOE-EPSILON-4; PEOPLE; ALLELE;
D O I
10.1016/j.nicl.2016.12.002
中图分类号
R445 [影像诊断学];
学科分类号
100207 ;
摘要
Increased fMRI activation in the hippocampus is recognized as a signature characteristic of the amnestic mild cognitive impairment (aMCI) stage of Alzheimer's disease (AD). Previous work has localized this increased activation to the dentate gyrus/CA3 subregion of the hippocampus and showed a correlation with memory impairments in those patients. Increased hippocampal activation has also been reported in carriers of the ApoE-4 allelic variation independently of mild cognitive impairment although these findings were not localized to a hippocampal subregion. To assess the ApoE-4 contribution to increased hippocampal fMRI activation, patients with aMCI genotyped for ApoE-4 status and healthy age-matched control participants completed a high-resolution fMRI scan while performing a memory task designed to tax hippocampal subregion specific functions. Consistent with previous reports, patients with aMCI showed increased hippocampal activation in the left dentate gyrus/CA3 region of the hippocampus as well as memory task errors attributable to this subregion. However, this increased fMRI activation in the hippocampus did not differ between ApoE-4 carriers and ApoE-4 non-carriers and the proportion of memory errors attributable to dentate gyrus/CA3 function did not differ between ApoE-4 carriers and ApoE-4 non-carriers. These results indicate that increased fMRI activation of the hippocampus observed in patients with aMCI is independent of ApoE-4 status and that ApoE-4 does not contribute to the dysfunctional hippocampal activation or the memory errors attributable to this subregion in these patients. (C) 2016 The Authors. Published by Elsevier Inc.
引用
收藏
页码:237 / 245
页数:9
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