Effects of PPP1R1B (DARPP-32) Polymorphism on Feedback-Related Brain Potentials Across the Life Span

被引:11
作者
Haemmerer, Dorothea [1 ,2 ]
Biele, Gudio [3 ,4 ]
Mueller, Viktor [1 ]
Thiele, Holger [5 ]
Nuernberg, Peter [5 ,6 ,7 ]
Heekeren, Hauke R. [1 ,3 ]
Li, Shu-Chen [1 ,2 ]
机构
[1] Max Planck Inst Human Dev, Ctr Lifespan Psychol, Berlin, Germany
[2] Tech Univ Dresden, Dept Psychol, D-01062 Dresden, Germany
[3] Free Univ Berlin, Dept Educ & Psychol, Berlin, Germany
[4] Univ Oslo, Inst Psychol, Oslo, Norway
[5] Univ Cologne, Cologne Ctr Genom, D-50931 Cologne, Germany
[6] Univ Cologne, Ctr Mol Med Cologne, D-50931 Cologne, Germany
[7] Univ Cologne, Cologne Excellence Cluster Cellular Stress Respon, D-50931 Cologne, Germany
来源
FRONTIERS IN PSYCHOLOGY | 2013年 / 4卷
关键词
PPP1R1B (DARPP-32); dopamine; reward; reinforcement learning; child development; aging; WORKING-MEMORY; PREFRONTAL CORTEX; DEVELOPMENTAL DIFFERENCES; INDIVIDUAL-DIFFERENCES; COGNITIVE CONTROL; DECISION-MAKING; DOPAMINE SYSTEM; AGE; INHIBITION; NEUROMODULATION;
D O I
10.3389/fpsyg.2013.00089
中图分类号
B84 [心理学];
学科分类号
04 ; 0402 ;
摘要
Maximizing gains during probabilistic reinforcement learning requires the updating of choice - outcome expectations at the time when the feedback about a specific choice or action is given. Extant theories and evidence suggest that dopaminergic modulation plays a crucial role in reinforcement learning and the updating of choice - outcome expectations. Furthermore, recently a positive component of the event-related potential about 200?ms (P2) after feedback has been suggested to reflect such updating. The efficacy of dopaminergic modulation changes across the life span. However, to date investigations of age-related differences in feedback-related P2 during reinforcement learning are still scarce. The present study thus aims to investigate whether individual differences in the feedback-related P2 would be associated with polymorphic variations in a dopamine relevant gene PPP1R1B (also known as DARPP-32) and whether the genetic effect may differ between age groups. We observed larger P2 amplitudes in individuals carrying the genotype associated with higher dopamine receptor efficacy, i.e., a allele homozygotes of a single nucleotide polymorphism (rs907094) of the PPP1R1B gene. Moreover, this effect was more pronounced in children and older adults in comparison to adolescents and younger adults. Together, our findings indicate that polymorphic variations in a dopamine relevant gene are associated with individual differences in brain-evoked potentials of outcome updating and hint at the possibility that genotype effects on neurocognitive phenotypes may vary as a function of brain maturation and aging.
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页数:8
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