Reduced hippocampal CA2, CA3, and dentate gyrus activity in asymptomatic people at genetic risk for Alzheimer's disease

被引:20
|
作者
Suthana, Nanthia A. [1 ,2 ]
Krupa, Allison [1 ,2 ]
Donix, Markus [1 ,2 ,5 ]
Burggren, Alison [1 ,2 ]
Ekstrom, Arne D. [6 ,7 ]
Jones, Michael [1 ,2 ]
Ercoli, Linda M. [2 ,3 ,4 ]
Miller, Karen J. [2 ,3 ,4 ]
Siddarth, Prabha [2 ,3 ,4 ]
Small, Gary W. [2 ,3 ,4 ]
Bookheimer, Susan Y. [1 ,2 ]
机构
[1] Univ Calif Los Angeles, Semel Inst, Ctr Cognit Neurosci, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Semel Inst, Dept Psychiat & Biobehav Sci, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Semel Inst, Div Geriatr Psychiat, Los Angeles, CA 90095 USA
[4] Univ Calif Los Angeles, Semel Inst, Memory & Aging Res Ctr, Los Angeles, CA 90095 USA
[5] Tech Univ Dresden, Univ Klinikum Carl Gustav Carus, Dept Psychiat & Psychotherapy, Dresden, Germany
[6] Univ Calif Davis, Ctr Neurosci, Davis, CA 95616 USA
[7] Univ Calif Davis, Dept Psychol, Davis, CA 95616 USA
关键词
Alzheimer's disease; ApoE; Hippocampus; MRI; fMRI; High-resolution imaging; APOLIPOPROTEIN-E; FUNCTIONAL MRI; ENTORHINAL CORTEX; COGNITIVE DECLINE; BRAIN ACTIVATION; TRANSGENIC MICE; FMRI EVIDENCE; OLDER-ADULTS; MEMORY; TOMOGRAPHY;
D O I
10.1016/j.neuroimage.2009.12.014
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Previous functional magnetic resonance imaging (MRI) studies in healthy subjects with the apolipoprotein E epsilon 4 (APOE-4) genetic risk for Alzheimer's disease have shown increased activation during memory task performance in broadly distributed cortical regions. These findings have been hypothesized to reflect compensatory recruitment of intact brain regions that presumably result from subtle neural dysfunction reflecting incipient disease. In this study, we used high-resolution functional MRI in APOE-4 carriers and non-carriers to measure activity in hippocampal subregions (CA fields 1, 2, 3; dentate gyrus [DG], and subiculum) and adjacent medial temporal lobe (parahippocampal and entorhinal) subregions. We found reduced left CA2, CA3, and dentate gyrus (CA23DG) activity in cognitively intact APOE-4 carriers. These results suggest that reduced neural activity in hippocampal subregions may underlie the compensatory increase in extrahippocampal activity in people with a genetic risk for Alzheimer's disease prior to the onset of cognitive deficits. (c) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:1077 / 1084
页数:8
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