Altered deactivation in individuals with genetic risk for Alzheimer's disease

被引:77
|
作者
Persson, J. [1 ]
Lind, J. [2 ]
Larsson, A. [3 ]
Ingvar, M. [2 ]
Sleegers, K. [4 ,5 ]
Van Broeckhoven, C. [4 ,5 ]
Adolfsson, R.
Nilsson, L. -G. [1 ]
Nyberg, L. [6 ]
机构
[1] Univ Stockholm, Dept Psychol, S-10691 Stockholm, Sweden
[2] Karolinska Hosp, MR Res Ctr, S-17176 Stockholm, Sweden
[3] Umea Univ, Dept Radiat Sci Radiat Phys, S-90187 Umea, Sweden
[4] Univ Antwerp VIB, Dept Mol Genet, Neurodegenerat Brain Dis Grp, B-2610 Antwerp, Belgium
[5] Univ Antwerp, B-2020 Antwerp, Belgium
[6] Umea Univ, Dept Radiat Sci Diagnost Radiol & Integrat Med Bi, Physiol Sect, S-90187 Umea, Sweden
关键词
deactivation; aging; APOE; genetic; AD; Alzheimer's disease; fMRI; compensation; memory encoding;
D O I
10.1016/j.neuropsychologia.2008.01.026
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Regions that show task-induced deactivations maybe part of a default-mode network related to processes that are more engaged during passive than active task conditions. Alteration of task-induced deactivations with age and dementia is indicated by atypical engagement of default-mode network regions. Genetic studies show a relation between the apolipoprotein E4 (APOE4) allele and the common form of Alzheimer's disease (AD), and altered functional brain activation has been observed in non-demented APOE4 carriers compared to non-carriers. Here we investigate the hypothesis of altered default-mode network brain responses in individuals with genetic risk for AD. Functional MRI was used to assess task-induced deactivation in 60 subjects of which 30 carried at least one copy of the APOE4 allele, and 30 non-carriers. Subjects were scanned while performing a semantic categorization task shown to promote episodic memory encoding. The results show patterns of deactivation consistent with the default-mode network. We also found reduced deactivation in non-demented APOE4 carriers compared to non-carriers, suggesting alterations in the default-mode network in the absence of dementia. These results implicate possibilities for investigating altered properties of task-induced deactivations in individuals with genetic risk for AD, and may prove useful for pre-clinical identification of individuals susceptible to memory problems and AD. (c) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1679 / 1687
页数:9
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