DNA Methylation in Autism Spectrum Disorders: Biomarker or Pharmacological Target?
Hanieh GholamalizadehMaedeh Amiri-ShahriFatemeh RasouliArina AnsariVafa Baradaran RahimiVahid Reza AskariPublished in: Brain sciences (2024)
Autism spectrum disorder (ASD) is a group of heterogeneous neurodevelopmental disabilities with persistent impairments in cognition, communication, and social behavior. Although environmental factors play a role in ASD etiopathogenesis, a growing body of evidence indicates that ASD is highly inherited. In the last two decades, the dramatic rise in the prevalence of ASD has interested researchers to explore the etiologic role of epigenetic marking and incredibly abnormal DNA methylation. This review aimed to explain the current understanding of the association between changes in DNA methylation signatures and ASD in patients or animal models. We reviewed studies reporting alterations in DNA methylation at specific genes as well as epigenome-wide association studies (EWASs). Finally, we hypothesized that specific changes in DNA methylation patterns could be considered a potential biomarker for ASD diagnosis and prognosis and even a target for pharmacological intervention.
Keyphrases
- autism spectrum disorder
- dna methylation
- genome wide
- attention deficit hyperactivity disorder
- intellectual disability
- gene expression
- copy number
- end stage renal disease
- randomized controlled trial
- healthcare
- chronic kidney disease
- newly diagnosed
- multiple sclerosis
- case control
- working memory
- transcription factor