Age-Related Effects of the Apolipoprotein E Gene on Brain Function

被引:18
|
作者
Matura, Silke [1 ,3 ]
Prvulovic, David [1 ]
Hartmann, Daniel [1 ]
Scheibe, Monika [1 ]
Sepanski, Beate [1 ]
Butz, Marius [1 ]
Oertel-Knoechel, Viola [1 ]
Knoechel, Christian [1 ]
Karakaya, Tarik [1 ]
Fusser, Fabian [1 ]
Hattingen, Elke [2 ]
Pantel, Johannes [3 ]
机构
[1] Goethe Univ Frankfurt, Dept Psychiat Psychosomat Med & Psychotherapy, Lab Neurophysiol & Neuroimaging, D-60590 Frankfurt, Germany
[2] Goethe Univ Frankfurt, Inst Neuroradiol, D-60590 Frankfurt, Germany
[3] Goethe Univ Frankfurt, Inst Gen Practice, D-60590 Frankfurt, Germany
关键词
Apolipoprotein; 4; brain; functional MRI; memory; APOE GENOTYPE; OLDER-ADULTS; ALZHEIMERS-DISEASE; COGNITIVE FUNCTION; WORKING-MEMORY; FMRI EVIDENCE; EPSILON-4; PERFORMANCE; ACTIVATION; DECLINE;
D O I
10.3233/JAD-150990
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The apolipoprotein E (ApoE) epsilon 4 allele is a well-established genetic risk factor for sporadic Alzheimer's disease. Some evidence suggests a negative role of the ApoE epsilon 4 allele for cognitive performance in late life, while beneficial effects on cognition have been shown in young age. We investigated age-related effects of the ApoE gene on brain function by assessing cognitive performance, as well as functional activation patterns during retrieval of Face-Name pairs in a group of young (n = 50; age 26.4 +/- 4.6 years, 25 epsilon 4 carriers) and old (n = 40; age 66.1 +/- 7.0 years, 20 epsilon 4 carriers) participants. A cross-sectional factorial design was used to examine the effects of age, ApoE genotype, and their interaction on both cognitive performance and the blood oxygenation level dependent (BOLD) brain response during retrieval of Face-Name pairs. While there were no genotype-related differences in cognitive performance, we found a significant interaction of age and ApoE genotype on task-related activation bilaterally in anterior cingulate gyrus and superior frontal gyrus, as well as left and right insula. Old age was associated with increased activity in epsilon 4 carriers. The increased BOLD response in old epsilon 4 carriers during retrieval could indicate a neurocognitive disadvantage associated with the epsilon 4 allele with increasing age. Furthermore, recruitment of neuronal resources resulted in enhanced memory performance in young epsilon 4 carriers, pointing to a better neurofunctional capacity associated with the ApoE4 genotype in young age.
引用
收藏
页码:317 / 331
页数:15
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