A common genetic variant in the Neurexin family member CNTNAP2 is related to language but not communication skills in youth with Autism Spectrum Disorder.

Vardan Arutiunian, Megha Santhosh, Emily Neuhaus, Catherine A W Sullivan, Raphael A Bernier, Susan Y Bookheimer, Mirella Dapretto, Daniel H Geschwind, Allison Jack, James C McPartland, John D Van Horn, Kevin A Pelphrey, Abha R Gupta, Sara Jane Webb
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Abstract

One of the candidate genes related to language variability in individuals with Autism Spectrum Disorder (ASD) is the contactin-associated protein-like 2 gene (CNTNAP2), a member of the Neurexin family. However, due to the different assessment tools used, it is unknown whether the polymorphisms of the CNTNAP2 gene are linked to structural language skills or more general communication abilities. A total of 302 youth aged 7 to 18 years participated in the present study: 131 verbal youth with ASD (62 female), 130 typically developing (TD) youth (64 female), and 41 unaffected siblings (US) of youth with ASD (25 female). Blood samples were collected to obtain genomic DNA and processed by the Rutgers University Cell and Data Repository or using standard protocols (Gentra Puregene Blood DNA extraction kit; Qiagen). Language and verbal communication skills were screened with the Clinical Evaluation of Language Fundamental-4 (CELF-4) and Vineland-II Communication domain, subsequently. The results showed that the polymorphism of CNTNAP2 (SNP rs2710102) was related to structural language abilities, such that participants carrying the A-allele had lower language skills in comparison to the G-allele homozygotes. No relationship was found between the polymorphism of CNTNAP2 and more general communication abilities. Although the study revealed genetic mechanisms that are associated with CELF-4 measures but not Vineland-II in youth with ASD, follow-up studies are needed that will include measures of language and communication that are less correlated to each other as well as will include a group of minimally and/or non-verbal individuals with ASD.

神经肽家族成员 CNTNAP2 的常见基因变异与自闭症谱系障碍青少年的语言能力有关,但与沟通能力无关。
与自闭症谱系障碍(ASD)患者的语言变异有关的候选基因之一是接触蛋白相关蛋白样 2 基因(CNTNAP2),它是 Neurexin 家族的成员。然而,由于使用的评估工具不同,CNTNAP2 基因的多态性是与结构性语言技能有关,还是与更普遍的沟通能力有关,目前尚不得而知。共有 302 名 7 至 18 岁的青少年参与了本研究:其中包括 131 名患有自闭症的言语障碍青少年(62 名女性)、130 名发育典型(TD)青少年(64 名女性)以及 41 名患有自闭症的未受影响兄弟姐妹(US)(25 名女性)。采集血液样本以获得基因组 DNA,并由罗格斯大学细胞和数据储存库或采用标准方案(Gentra Puregene 血液 DNA 提取试剂盒;Qiagen)进行处理。随后,使用临床语言基础评估-4(CELF-4)和 Vineland-II 沟通域对语言和口头沟通能力进行了筛查。结果显示,CNTNAP2的多态性(SNP rs2710102)与结构性语言能力有关,携带A等位基因的参与者的语言能力低于携带G等位基因的同卵者。CNTNAP2 的多态性与更一般的沟通能力之间没有关系。尽管这项研究揭示了与 CELF-4 测量相关的遗传机制,但与患有 ASD 的青少年的 Vineland-II 无关,因此还需要进行后续研究,这些研究将包括相互关联度较低的语言和沟通测量,并将包括一组患有 ASD 的弱智和/或无语言能力的人。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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