Distinct patterns of brain activity in young carriers of the APOE-ε4 allele

被引:1334
作者
Filippini, Nicola [1 ,2 ,3 ]
MacIntosh, Bradley J. [2 ]
Hough, Morgan G. [2 ]
Goodwin, Guy M. [1 ]
Frisoni, Giovanni B. [3 ]
Smith, Stephen M. [2 ]
Matthews, Paul M. [4 ,5 ]
Beckmann, Christian F. [2 ,5 ]
Mackay, Clare E. [1 ,2 ]
机构
[1] Univ Oxford, Univ Dept Psychiat, Oxford OX3 9DU, England
[2] Univ Oxford, Funct Magnet Resonance Imaging Brain Ctr, Oxford OX3 9DU, England
[3] Ist Ricovero & Cura Carattere Sci San Giovanni di, Lab Epidemiol Neuroimaging & Telemed, I-25125 Brescia, Italy
[4] GlaxoSmithKline Inc, Res & Dev, Clin Imaging Ctr, London W12 0NN, England
[5] Univ London Imperial Coll Sci Technol & Med, Dept Clin Neurosci, London W12 0NN, England
关键词
hippocampus; memory; neuroimaging; resting connectivity; APOLIPOPROTEIN-E POLYMORPHISM; POSITRON-EMISSION-TOMOGRAPHY; COGNITIVELY INTACT ADULTS; CORONARY-ARTERY-DISEASE; LONG-TERM POTENTIATION; APOE EPSILON-4 ALLELE; MEDIAL TEMPORAL-LOBE; ALZHEIMERS-DISEASE; GENETIC RISK; DEFAULT-MODE;
D O I
10.1073/pnas.0811879106
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The APOE epsilon 4 allele is a risk factor for late-life pathological changes that is also associated with anatomical and functional brain changes in middle-aged and elderly healthy subjects. We investigated structural and functional effects of the APOE polymorphism in 18 young healthy APOE epsilon 4-carriers and 18 matched noncarriers (age range: 20-35 years). Brain activity was studied both at rest and during an encoding memory paradigm using blood oxygen level-dependent fMRI. Resting fMRI revealed increased "default mode network'' (involving retrosplenial, medial temporal, and medial-prefrontal cortical areas) coactivation in epsilon 4-carriers relative to noncarriers. The encoding task produced greater hippocampal activation in epsilon 4-carriers relative to noncarriers. Neither result could be explained by differences in memory performance, brain morphology, or resting cerebral blood flow. The APOE epsilon 4 allele modulates brain function decades before any clinical or neurophysiological expression of neurodegenerative processes.
引用
收藏
页码:7209 / 7214
页数:6
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