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健康成年人中 COMT Val158Met 基因型与执行功能的个体差异。

COMT Val158Met Genotype and Individual Differences in Executive Function in Healthy Adults.

机构信息

Department of Psychiatry, Dartmouth Medical School, Lebanon, New Hampshire 03756-0001, USA.

出版信息

J Int Neuropsychol Soc. 2011 Jan;17(1):174-80. doi: 10.1017/S1355617710001402. Epub 2010 Dec 10.

Abstract

The Val158Met polymorphism of the catechol-O-methyltransferase (COMT) gene may be related to individual differences in cognition, likely via modulation of prefrontal dopamine catabolism. However, the available studies have yielded mixed results, possibly in part because they do not consistently account for other genes that affect cognition. We hypothesized that COMT Met allele homozygosity, which is associated with higher levels of prefrontal dopamine, would predict better executive function as measured using standard neuropsychological testing, and that other candidate genes might interact with COMT to modulate this effect. Participants were 95 healthy, right-handed adults who underwent genotyping and cognitive testing. COMT genotype predicted executive ability as measured by the Trail-Making Test, even after covarying for demographics and Apolipoprotein E (APOE), brain-derived neurotrophic factor (BDNF), and ankyrin repeat and kinase domain containing 1 (ANKK1) genotype. There was a COMT-ANKK1 interaction in which individuals having both the COMT Val allele and the ANKK1 T allele showed the poorest performance. This study suggests the heterogeneity in COMT effects reported in the literature may be due in part to gene-gene interactions that influence central dopaminergic systems.

摘要

儿茶酚-O-甲基转移酶(COMT)基因的 Val158Met 多态性可能与认知个体差异有关,可能通过调节前额叶多巴胺的分解代谢。然而,现有的研究结果喜忧参半,部分原因可能是它们没有始终如一地考虑到影响认知的其他基因。我们假设 COMT Met 等位基因纯合子与前额叶多巴胺水平升高有关,这将预测使用标准神经心理学测试测量的执行功能更好,而其他候选基因可能与 COMT 相互作用以调节这种影响。参与者是 95 名健康的右利手成年人,他们接受了基因分型和认知测试。即使在协变量为人口统计学和载脂蛋白 E(APOE)、脑源性神经营养因子(BDNF)和锚蛋白重复和激酶结构域包含 1(ANKK1)基因型后,COMT 基因型也预测了执行能力,如 Trail-Making 测试所示。COMT-ANKK1 相互作用中,同时具有 COMT Val 等位基因和 ANKK1 T 等位基因的个体表现最差。这项研究表明,文献中报道的 COMT 效应的异质性部分可能是由于影响中枢多巴胺能系统的基因-基因相互作用所致。

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