Abstract
AbstractThe 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 genesOXTRandAVPR1A, 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. HigherOXTRandAVPR1Aexpression was associated with lower Aberrant Behavior Checklist (ABC) scores.OXTRexpression was associated with less severe behavior and higher adaptive behavior on additional standardized measures. Combining the sum expression levelsOXTR,AVPR1A, andIGF1yielded 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 ofOXTR,AVPR1A, andIGF1.
Publisher
Springer Science and Business Media LLC
Cited by
16 articles.
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