COMT val158met predicts reward responsiveness in humans

被引:28
作者
Lancaster, T. M. [1 ,4 ]
Linden, D. E. [2 ,3 ]
Heerey, E. A. [4 ]
机构
[1] Bangor Univ, Sch Med Sci, Bangor LL57 2AS, Gwynedd, Wales
[2] MRC Ctr Neuropsychiat Genet & Genom, Inst Psychol Med & Clin Neurosci, Cardiff, S Glam, Wales
[3] Cardiff Univ, Sch Psychol, Cardiff CF10 3AX, S Glam, Wales
[4] Bangor Univ, Sch Psychol, Bangor LL57 2AS, Gwynedd, Wales
基金
英国生物技术与生命科学研究理事会;
关键词
COMT; decision-making; dopamine; genetics; individual differences; reward; risk-taking; CATECHOL-O-METHYLTRANSFERASE; VAL(158)MET POLYMORPHISM; RISK-TAKING; PREFRONTAL CORTEX; GENETIC-VARIATION; HEDONIC CAPACITY; DOPAMINE; TASK; HERITABILITY; METAANALYSIS;
D O I
10.1111/j.1601-183X.2012.00838.x
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
A functional variant of the catechol-O-methyltransferase (COMT) gene [val158met (rs4680)] is frequently implicated in decision-making and higher cognitive functions. It may achieve its effects by modulating dopamine-related decision-making and reward-guided behaviour. Here we demonstrate that individuals with the met/met polymorphism have greater responsiveness to reward than carriers of the val allele and that this correlates with risk-seeking behaviour. We assessed performance on a reward responsiveness task and the Balloon analogue risk task, which measure how participants (N = 70, western European, university and postgraduate students) respond to reward and take risks in the presence of available reward. Individuals with the met/met genotype (n = 19) showed significantly higher reward responsiveness, F-2,F-64 = 4.02, P = 0.02, and reward-seeking behaviour, F (2,68)= 4.52, P = 0.01, than did either val/met (n = 25) or val/val (n = 26) carriers. These results highlight a scenario in which genotype-dependent reward responsiveness shapes reward-seeking, therefore suggesting a novel framework by which COMT may modulate behaviour.
引用
收藏
页码:986 / 992
页数:7
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