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首页> 外文期刊>Autism research: official journal of the International Society for Autism Research >Language Impairment and Dyslexia Genes Influence Language Skills in Children With Autism Spectrum Disorders
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Language Impairment and Dyslexia Genes Influence Language Skills in Children With Autism Spectrum Disorders

机译:语言障碍和阅读障碍基因影响自闭症谱系障碍儿童的语言技能

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Language and communication development is a complex process influenced by numerous environmental and genetic factors. Many neurodevelopment disorders include deficits in language and communication skills in their diagnostic criteria, including autism spectrum disorders (ASD), language impairment (LI), and dyslexia. These disorders are polygenic and complex with a significant genetic component contributing to each. The similarity of language phenotypes and comorbidity of these disorders suggest that they may share genetic contributors. To test this, we examined the association of genes previously implicated in dyslexia, LI, and/or language-related traits with language skills in children with ASD. We used genetic and language data collected in the Autism Genome Research Exchange (AGRE) and Simons Simplex Collection (SSC) cohorts to perform a meta-analysis on performance on a receptive vocabulary task. There were associations with LI risk gene ATP2C2 and dyslexia risk gene MRPL19. Additionally, we found suggestive evidence of association with CMIP, GCFC2, KIAA0319L, the DYX2 locus (ACOT13, GPLD1, and FAM65B), and DRD2. Our results show that LI and dyslexia genes also contribute to language traits in children with ASD. These associations add to the growing literature of generalist genes that contribute to multiple related neurobehavioral traits. Future studies should examine whether other genetic contributors may be shared among these disorders and how risk variants interact with each other and the environment to modify clinical presentations. Autism Res 2015, 8: 229-234. (c) 2014 International Society for Autism Research, Wiley Periodicals, Inc.
机译:语言和交流的发展是一个受许多环境和遗传因素影响的复杂过程。许多神经发育障碍的诊断标准包括语言和沟通技巧的缺陷,包括自闭症谱系障碍(ASD),语言障碍(LI)和阅读障碍。这些疾病是多基因的,并且是复杂的,并且每种疾病都有重要的遗传成分。语言表型的相似性和这些疾病的合并症表明它们可能共享遗传因素。为了测试这一点,我们检查了先前与阅读障碍,LI和/或语言相关性状有关的基因与ASD儿童的语言技能之间的关联。我们使用自闭症基因组研究交流中心(AGRE)和西蒙斯单纯形收藏(SSC)队列中收集的遗传和语言数据,对接受词汇任务的表现进行了荟萃分析。与LI风险基因ATP2C2和阅读障碍风险基因MRPL19相关。此外,我们发现与CMIP,GCFC2,KIAA0319L,DYX2基因座(ACOT13,GPLD1和FAM65B)和DRD2相关的暗示证据。我们的结果表明,LI和阅读障碍基因也有助于ASD儿童的语言特征。这些关联为越来越多的通才基因提供了文献资料,这些基因有助于多种相关的神经行为特征。未来的研究应检查这些疾病中是否可能存在其他遗传因素,以及风险变量如何相互影响以及环境如何相互作用以改变临床表现。自闭症研究2015,8:229-234。 (c)2014年国际自闭症研究协会,Wiley Periodicals,Inc.。

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