Uncovering convergence and divergence between autism and schizophrenia using genomic tools and patients' neurons.
Eva RomanovskyAshwani ChoudharyDavid PelesAhmad M Abu-AkelShani SternPublished in: Molecular psychiatry (2024)
Autism spectrum disorders (ASDs) are highly heritable and result in abnormal repetitive behaviors and impairment in communication and cognitive skills. Previous studies have focused on the genetic correlation between ASDs and other neuropsychiatric disorders, but an in-depth understanding of the correlation to other disorders is required. We conducted an extensive meta-analysis of common variants identified in ASDs by genome-wide association studies (GWAS) and compared it to the consensus genes and single nucleotide polymorphisms (SNPs) of Schizophrenia (SCZ). We found approximately 75% of the GWAS genes that are associated with ASD are also associated with SCZ. We further investigated the cellular phenotypes of neurons derived from induced pluripotent stem cell (iPSC) models in ASD and SCZ. Our findings revealed that ASD and SCZ neurons initially follow divergent developmental trajectories compared to control neurons. However, despite these early diametrical differences, both ASD and SCZ neurons ultimately display similar deficits in synaptic activity as they mature. This significant genetic overlap between ASD and SCZ, coupled with the convergence towards similar synaptic deficits, highlights the intricate interplay of genetic and developmental factors in shaping the shared underlying mechanisms of these complex neurodevelopmental and neuropsychiatric disorders.
Keyphrases
- autism spectrum disorder
- genome wide
- intellectual disability
- attention deficit hyperactivity disorder
- spinal cord
- copy number
- stem cells
- genome wide association
- bipolar disorder
- traumatic brain injury
- end stage renal disease
- dna methylation
- newly diagnosed
- ejection fraction
- chronic kidney disease
- prognostic factors
- gene expression
- peritoneal dialysis
- spinal cord injury
- mesenchymal stem cells
- clinical practice
- single cell
- optical coherence tomography
- transcription factor
- genome wide association study