Autism spectrum disorders: autistic phenotypes and complicated mechanisms

World J Pediatr. 2019 Feb;15(1):17-25. doi: 10.1007/s12519-018-0210-2. Epub 2019 Jan 3.

Abstract

Background: Autism spectrum disorder (ASD), a pervasive developmental neurological disorder, is characterized by impairments in social interaction and communication, and stereotyped, repetitive patterns of interests or behaviors. The mechanism of ASDs is complex, and genetic components and epigenetic modifications play important roles. In this review, we summarized the recent progresses of ASDs focusing on the genetic and epigenetic mechanisms. We also briefly discussed current animal models of ASD and the application of high-throughput sequencing technologies in studying ASD.

Data sources: Original research articles and literature reviews published in PubMed-indexed journals.

Results: Individuals with ASDs exhibit a set of phenotypes including neurological alteration. Genetic components including gene mutation, copy-number variations, and epigenetic modifications play important and diverse roles in ASDs. The establishment of animal models and development of new-generation sequencing technologies have contributed to reveal the complicated mechanisms underlying autistic phenotypes.

Conclusions: Dramatic progress has been made for understanding the roles of genetic and epigenetic components in ASD. Future basic and translational studies should be carried out towards those candidate therapeutic targets.

Keywords: Autism spectrum disorders; CNV; Epigenetics; Genetics; Next-generation sequencing.

Publication types

  • Review

MeSH terms

  • Animals
  • Autism Spectrum Disorder / genetics*
  • DNA Copy Number Variations
  • DNA Methylation
  • Disease Models, Animal
  • Epigenesis, Genetic
  • Genetic Variation
  • Genome-Wide Association Study
  • High-Throughput Nucleotide Sequencing
  • Humans
  • Mutation
  • Phenotype