Ebbinghaus Revisited: Influences of the BDNF Val66Met Polymorphism on Backward Serial Recall Are Modulated by Human Aging

被引:50
作者
Li, Shu-Chen [1 ,2 ]
Chicherio, Christian [3 ]
Nyberg, Lars [4 ]
von Oertzen, Timo
Nagel, Irene E. [2 ]
Papenberg, Goran
Sander, Thomas [5 ]
Heekeren, Hauke R. [2 ,6 ,7 ]
Lindenberger, Ulman [2 ]
Baeckman, Lars [2 ,8 ]
机构
[1] Max Planck Inst Human Dev, Ctr Lifespan Psychol, D-14195 Berlin, Germany
[2] Berlin Neuroimaging Ctr, Berlin, Germany
[3] Univ Geneva, Geneva, Switzerland
[4] Umea Univ, Umea, Sweden
[5] Cologne Ctr Genom, Cologne, Germany
[6] Charite, D-13353 Berlin, Germany
[7] Max Planck Inst Cognit & Brain Sci, Leipzig, Germany
[8] Karolinska Inst, Stockholm, Sweden
基金
瑞典研究理事会;
关键词
NEUROTROPHIC FACTOR VAL66MET; SHORT-TERM-MEMORY; WORKING-MEMORY; HIPPOCAMPAL ACTIVITY; FACTOR GENE; LIFE-SPAN; COGNITIVE-ABILITIES; ORDER INFORMATION; EPISODIC MEMORY; BRAIN;
D O I
10.1162/jocn.2009.21374
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The brain-derived neurotrophic factor (BDNF) plays an important role in activity-dependent synaptic plasticity, which underlies learning and memory. In a sample of 948 younger and older adults, we investigated whether a common Val66Met missense polymorphism (rs6265) in the BDNF gene affects the serial position curve-a fundamental phenomenon of associative memory identified by Hermann Ebbinghaus more than a century ago. We found a BDNF polymorphism effect for backward recall in older adults only, with Met-allele carriers (i.e., individuals with reduced BDNF signaling) recalling fewer items than Val homozygotes. This effect was specific to the primacy and middle portions of the serial position curve, where intralist interference and associative demands are especially high. The poorer performance of older Met-allele carriers reflected transposition errors, whereas no genetic effect was found for omissions. These findings indicate that effects of the BDNF polymorphism on episodic memory are most likely to be observed when the associative and executive demands are high. Furthermore, the findings are in line with the hypothesis that the magnitude of genetic effects on cognition is greater when brain resources are reduced, as is the case in old age.
引用
收藏
页码:2164 / 2173
页数:10
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