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1
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Infancy. 2001 Jul;2(3):311-330. doi: 10.1207/S15327078IN0203_2. Epub 2001 Jul 1.
2
COMT val108/158 met genotype affects neural but not cognitive processing in healthy individuals.COMT val108/158 met 基因型影响健康个体的神经但不影响认知加工。
Cereb Cortex. 2010 Mar;20(3):672-83. doi: 10.1093/cercor/bhp132. Epub 2009 Jul 29.
3
Neural substrates of pleiotropic action of genetic variation in COMT: a meta-analysis.COMT 基因变异的多效性作用的神经基础:荟萃分析。
Mol Psychiatry. 2010 Sep;15(9):918-27. doi: 10.1038/mp.2009.36. Epub 2009 May 5.
4
Striatal dopamine transporter availability associated with polymorphisms in the dopamine transporter gene SLC6A3.纹状体多巴胺转运体可用性与多巴胺转运体基因SLC6A3中的多态性相关。
J Nucl Med. 2009 Jan;50(1):45-52. doi: 10.2967/jnumed.108.053652. Epub 2008 Dec 17.
5
Effect of COMT val158met genotype on cognition and personality.儿茶酚-O-甲基转移酶(COMT)val158met基因型对认知和个性的影响。
Eur Psychiatry. 2008 Sep;23(6):385-9. doi: 10.1016/j.eurpsy.2008.05.002. Epub 2008 Aug 27.
6
Genetic dissection of the role of catechol-O-methyltransferase in cognition and stress reactivity in mice.儿茶酚-O-甲基转移酶在小鼠认知和应激反应中作用的遗传学剖析
J Neurosci. 2008 Aug 27;28(35):8709-23. doi: 10.1523/JNEUROSCI.2077-08.2008.
7
Dopamine transporter polymorphism modulates oculomotor function and DAT1 mRNA expression in schizophrenia.多巴胺转运体基因多态性调节精神分裂症患者的眼球运动功能及多巴胺转运体1(DAT1)信使核糖核酸(mRNA)表达。
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8
Prefrontal cortical involvement in young infants' analysis of novelty.前额叶皮质参与幼儿对新奇事物的分析。
Cereb Cortex. 2009 Feb;19(2):455-63. doi: 10.1093/cercor/bhn096. Epub 2008 Jun 9.
9
Functional connectivity of human striatum: a resting state FMRI study.人类纹状体的功能连接性:一项静息态功能磁共振成像研究。
Cereb Cortex. 2008 Dec;18(12):2735-47. doi: 10.1093/cercor/bhn041. Epub 2008 Apr 9.
10
Meta-analysis of the cognitive effects of the catechol-O-methyltransferase gene Val158/108Met polymorphism.儿茶酚-O-甲基转移酶基因Val158/108Met多态性认知效应的荟萃分析。
Biol Psychiatry. 2008 Jul 15;64(2):137-44. doi: 10.1016/j.biopsych.2008.01.005. Epub 2008 Mar 14.

多巴胺系统基因多态性与婴儿期注意力个体差异有关。

Polymorphisms in dopamine system genes are associated with individual differences in attention in infancy.

机构信息

Centre for Brain and Cognitive Development, Birkbeck, University of London, London, United Kingdom.

出版信息

Dev Psychol. 2010 Mar;46(2):404-16. doi: 10.1037/a0018180.

DOI:10.1037/a0018180
PMID:20210499
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3276838/
Abstract

Knowledge about the functional status of the frontal cortex in infancy is limited. This study investigated the effects of polymorphisms in four dopamine system genes on performance in a task developed to assess such functioning, the Freeze-Frame task, at 9 months of age. Polymorphisms in the catechol-O-methyltransferase (COMT) and the dopamine D4 receptor (DRD4) genes are likely to impact directly on the functioning of the frontal cortex, whereas polymorphisms in the dopamine D2 receptor (DRD2) and dopamine transporter (DAT1) genes might influence frontal cortex functioning indirectly via strong frontostriatal connections. A significant effect of the COMT valine(1)methionine (Val 158 Met) polymorphism was found. Infants with the Met/Met genotype were significantly less distractible than infants with the Val/Val genotype in Freeze-Frame trials presenting an engaging central stimulus. In addition, there was an interaction with the DAT1 3; variable number of tandem repeats polymorphism; the COMT effect was present only in infants who did not have two copies of the DAT1 10-repeat allele. These findings indicate that dopaminergic polymorphisms affect selective aspects of attention as early as infancy and further validate the Freeze-Frame task as a frontal cortex task.

摘要

关于婴儿期额叶皮质功能状态的知识有限。本研究探讨了四种多巴胺系统基因中的多态性对 9 个月大时进行的一项评估这种功能的任务(冻结帧任务)表现的影响。儿茶酚-O-甲基转移酶(COMT)和多巴胺 D4 受体(DRD4)基因的多态性可能直接影响额叶皮质的功能,而多巴胺 D2 受体(DRD2)和多巴胺转运蛋白(DAT1)基因的多态性可能通过强烈的额纹状体连接间接影响额叶皮质功能。发现 COMT 缬氨酸(1)蛋氨酸(Val158Met)多态性有显著影响。在呈现吸引人的中央刺激的冻结帧试验中,携带 Met/Met 基因型的婴儿比携带 Val/Val 基因型的婴儿的注意力分散性明显降低。此外,还存在与 DAT1 3 的相互作用;可变数串联重复多态性;仅在没有 DAT1 10 重复等位基因的两个拷贝的婴儿中存在 COMT 效应。这些发现表明,多巴胺能多态性早在婴儿期就会影响注意力的选择性方面,并进一步验证了冻结帧任务作为额叶任务的有效性。