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

Author:

Arutiunian Vardan1ORCID,Santhosh Megha1,Neuhaus Emily12ORCID,Sullivan Catherine A. W.3ORCID,Bernier Raphael A.2ORCID,Bookheimer Susan Y.45,Dapretto Mirella45ORCID,Geschwind Daniel H.4567,Jack Allison8,McPartland James C.9,Van Horn John D.1011,Pelphrey Kevin A.12,Gupta Abha R.3913,Webb Sara Jane12ORCID,

Affiliation:

1. Center for Child Health, Behavior and Development Seattle Children's Research Institute Seattle Washington USA

2. Department of Psychiatry and Behavioral Science University of Washington Seattle Washington USA

3. Department of Pediatrics Yale School of Medicine New Haven Connecticut USA

4. Department of Psychiatry and Biobehavioral Sciences, Semel Institute for Neuroscience and Human Behavior, David Geffen School of Medicine University of California Los Angeles Los Angeles California USA

5. Center for Autism Research and Treatment, Semel Institute for Neuroscience and Human Behavior, David Geffen School of Medicine University of California Los Angeles Los Angeles California USA

6. Department of Neurology, David Geffen School of Medicine University of California Los Angeles Los Angeles California USA

7. Department of Human Genetics, David Geffen School of Medicine University of California Los Angeles Los Angeles California USA

8. Department of Psychology George Mason University Fairfax Virginia USA

9. Yale Child Study Center Yale School of Medicine New Haven Connecticut USA

10. Department of Psychology University of Virginia Charlottesville Virginia USA

11. School of Data Science University of Virginia Charlottesville Virginia USA

12. Department of Neurology, School of Medicine University of Virginia Virginia USA

13. Department of Neuroscience Yale School of Medicine New Haven Connecticut USA

Abstract

AbstractOne 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.

Funder

National Institute of Mental Health

Publisher

Wiley

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