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The COMT Val/Met polymorphism is associated with reading related skills and consistent patterns of functional neural activation

机译:该COmT缬氨酸/会见多态性与阅读相关的技能和功能性神经激活的一贯模式相关

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摘要

In both children and adults there is large variability in reading skill, with approximately 5–10% of individuals characterized as having reading disability; these individuals struggle to learn to read despite adequate intelligence and opportunity. Although it is well established that a substantial portion of this variability is attributed to the genetic differences between individuals, specifics of the connections between reading and the genome are not understood. This article presents data that suggest that variation in the COMT gene, which has previously been associated with variation in higher-order cognition, is associated with reading and reading-related skills, both at the level of brain and behavior. In particular, we found that the COMT Val/Met polymorphism at rs4680, which results in the substitution of the ancestral Valine (Val) by Methionine (Met), was associated with better performance on a number of critical reading measures and with patterns of functional neural activation that have been linked to better readers. We argue that this polymorphism, known for its broad effects on cognition, may modulate (likely through frontal lobe function) reading skill.
机译:在儿童和成人中,阅读技巧都有很大的差异,大约5-10%的人具有阅读障碍的特征。尽管有足够的智力和机会,这些人仍努力学习阅读。尽管已经很好地确定了这种可变性的很大一部分归因于个体之间的遗传差异,但人们并不了解阅读和基因组之间的联系细节。本文提供的数据表明,COMT基因的变异以前与高阶认知的变异有关,在大脑和行为方面与阅读以及与阅读相关的技能有关。尤其是,我们发现rs4680处的COMT Val / Met多态性导致蛋氨酸(Met)取代了祖先的缬氨酸(Val),在许多关键阅读措施上具有更好的性能,并且与功能模式有关与更好的读者相关的神经激活。我们认为,这种多态性以其对认知的广泛影响而著称,可能会调节(可能通过额叶功能)阅读技巧。

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