Human aging magnifies genetic effects on executive functioning and working memory

被引:185
作者
Nagel, Irene E. [1 ,2 ]
Chicherio, Christian [1 ]
Li, Shu-Chen [1 ,2 ]
von Oertzen, Timo [1 ]
Sander, Thomas [3 ]
Villringer, Arno [2 ,4 ,5 ]
Heekeren, Hauke R. [1 ,2 ,4 ,5 ]
Backman, Lars [1 ,2 ,6 ]
Lindenberger, Ulman [1 ,2 ]
机构
[1] Max Planck Inst Human Dev, D-14195 Berlin, Germany
[2] Berlin Neuroimaging Ctr, Berlin, Germany
[3] Max Delbruck Ctr Mol Med, Berlin, Germany
[4] Charite, Dept Neurol, D-13353 Berlin, Germany
[5] Max Planck Inst Human Cognit & Brain Sci, Leipzig, Germany
[6] Karolinska Inst, Aging Res Ctr, Stockholm, Sweden
来源
FRONTIERS IN HUMAN NEUROSCIENCE | 2008年 / 2卷
基金
瑞典研究理事会;
关键词
genes; dopamine; executive functions; prefrontal cortex; aging;
D O I
10.3389/neuro.09.001.2008
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We demonstrate that common genetic polymorphisms contribute to the increasing heterogeneity of cognitive functioning in old age. We assess two common Val/Met polymorphisms, one affecting the Catechol-O-Methyltransferase (COMT) enzyme, which degrades dopamine (DA) in prefrontal cortex (PFC), and the other influencing the brain-derived neurotrophic factor (BDNF) protein. In two tasks (Wisconsin Card Sorting and spatial working memory), we find that effects of COMT genotype on cognitive performance are magnified in old age and modulated by BDNF genotype. Older COMT Val homozygotes showed particularly low levels of performance if they were also BDNF Met carriers. The age-associated magnification of COMT gene effects provides novel information on the inverted U-shaped relation linking dopaminergic neuromodulation in PFC to cognitive performance. The modulation of COMT effects by BDNF extends recent evidence of close interactions between frontal and medial-temporal circuitries in executive functioning and working memory.
引用
收藏
页数:8
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