Peripheral Blood Mononuclear Cell Oxytocin and Vasopressin Receptor Expression Positively Correlates with Social and Behavioral Function in Children with Autism.
Irena VoinskySirish C BennuriJulie SvigalsRichard Eugene FryeShannon RoseDavid GurwitzPublished in: Scientific reports (2019)
The peptide hormone oxytocin is an established regulator of social function in mammals, and dysregulated oxytocin signaling is implicated in autism spectrum disorder (ASD). Several clinical trials examining the effects of intranasal oxytocin for improving social and behavioral function in ASD have had mixed or inclusive outcomes. The heterogeneity in clinical trials outcomes may reflect large inter-individual expression variations of the oxytocin and/or vasopressin receptor genes OXTR and AVPR1A, respectively. To explore this hypothesis we examined the expression of both genes in peripheral blood mononuclear cells (PBMC) from ASD children, their non-ASD siblings, and age-matched neurotypical children aged 3 to 16 years of age as well as datamined published ASD datasets. Both genes were found to have large inter-individual variations. Higher OXTR and AVPR1A expression was associated with lower Aberrant Behavior Checklist (ABC) scores. OXTR expression was associated with less severe behavior and higher adaptive behavior on additional standardized measures. Combining the sum expression levels OXTR, AVPR1A, and IGF1 yielded the strongest correlation with ABC scores. We propose that future clinical trials in ASD children with oxytocin, oxytocin mimetics and additional tentative therapeutics should assess the prognostic value of their PBMC mRNA expression of OXTR, AVPR1A, and IGF1.
Keyphrases
- autism spectrum disorder
- poor prognosis
- intellectual disability
- clinical trial
- attention deficit hyperactivity disorder
- binding protein
- peripheral blood
- young adults
- healthcare
- mental health
- small molecule
- long non coding rna
- single cell
- randomized controlled trial
- bone marrow
- skeletal muscle
- mesenchymal stem cells
- transcription factor
- gene expression
- insulin resistance
- adipose tissue
- drug induced
- working memory
- glycemic control
- study protocol