Next-Generation Sequencing in Korean Children With Autism Spectrum Disorder and Comorbid Epilepsy.

Front Pharmacol

Division of Child and Adolescent Psychiatry, Department of Psychiatry, Severance Hospital, Institute of Behavioral Science in Medicine, Yonsei University College of Medicine, Seoul, South Korea.

Published: May 2020

AI Article Synopsis

  • Autism spectrum disorder (ASD) is a neurodevelopmental disorder that affects social communication and behavior, and understanding its genetic basis is crucial for diagnosis and treatment.
  • Next-generation sequencing (NGS) allows for simultaneous analysis of multiple genes, which can enhance our understanding of autism genetics and aid in identifying significant genetic variants associated with ASD.
  • The study reviewed genetic data from 137 individuals with ASD, finding a diagnostic yield of 17.51% and noting that pathogenic variants were more common in females, with implications for both ASD and comorbidity with epilepsy.

Article Abstract

Autism spectrum disorder (ASD) is a neurodevelopmental disorder characterized by impairments in social communication and restricted and repetitive behaviors and interests. Identifying the genetic background may be one of the key features for the future diagnosis and treatment of ASD. With the tremendous development in genetic diagnosis techniques, next-generation sequencing (NGS) can be used to analyze multiple genes simultaneously with a single test in laboratory and clinical settings and is well suited for investigating autism genetics. According to previous studies, there are two types of genetic variants in ASD, rare variants and common variants, and both are important in explaining pathogenesis. In this study, NGS data from 137 participants with ASD were reviewed retrospectively with consideration for comorbid epilepsy. Diagnostic yield was 17.51% (24/137), and pathogenic/likely pathogenic variants were seen more frequently in female participants. Fourteen participants were diagnosed with comorbid epilepsy, six of them had pathogenic/likely pathogenic variants (43%). Genes with variants of unknown significance (VOUS) which have one or more evidence of pathogenicity following the American College of Medical Genetics (ACMG) criteria were also reviewed in both ASD and ASD with comorbid epilepsy groups. We found that most frequently found VOUS genes have previously been reported as genes related to ASD or other developmental disorders. These results suggest that when interpreting the NGS results in the clinical setting, careful observation of VOUS with some pathological evidence might contribute to the discovery of genetic pathogenesis of neurodevelopmental disorders such as ASD and epilepsy.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7240034PMC
http://dx.doi.org/10.3389/fphar.2020.00585DOI Listing

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