Abstract

Autism Spectrum disorder is one of the commonest and most important neurodevelopmental conditions affecting children today. With an increasing prevalence and an unclear aetiology, it is imperative we find early markers of autism, which may facilitate early identification and intervention. Alterations of gestational cytokine profiles have been reported in mothers of autistic children. Increasing evidence suggests that the intrauterine environment is an important determinant of autism risk. This study aims to examine the mid-gestational serum cytokine profiles of the mothers of autistic children from a well-characterised birth cohort. A nested sub-cohort within a large mother–child birth cohort were identified based on a confirmed multi-disciplinary diagnosis of autism before the age 10 years and neuro-typical matched controls in a 2:1 ratio. IFN-γ, IL-1β, IL-4, IL-6, IL-8, IL-17A, GMCSF and TNFα were measured in archived maternal 20-week serum using MesoScale Diagnostics multiplex technology and validation of our IL-17A measurements was performed using an ultrasensitive assay. From a cohort of 2137 children, 25 had confirmed autism before 10 years and stored maternal serum from mid-gestation. We examined the sera of these 25 cases and 50 matched controls. The sex ratio was 4:1 males to females in each group, and the mean age at diagnosis was 5.09 years (SD 2.13). We found that concentrations of IL-4 were significantly altered between groups. The other analytes did not differ significantly using either multiplex or ultra-sensitive assays. In our well-characterised prospective cohort of autistic children, we confirmed mid-gestational alterations in maternal IL-4 concentrations in autism affected pregnancies versus matched controls. These findings add to promising evidence from animal models and retrospective screening programmes and adds to the knowledge in this field.

Highlights

  • Autism Spectrum disorder is one of the commonest and most important neurodevelopmental conditions affecting children today

  • We used the V-plex multi-spot Cytokine Panel 1 kit (LOT No: Z0047047) to examine IL-17A and GMCSF, and we examined IFN-γ, IL-1β, IL-4, IL-6, IL-8 and TNFα using the V-plex multi-spot Proinflammatory Panel 1 kit (LOT No: Z0047096)

  • We have shown that the expression of IL-4 in maternal serum is altered significantly between Autism spectrum disorder (ASD) affected and matched control groups at 20 weeks’ gestation in a small, but carefully characterised cohort of mothers and children where the child has a diagnosis of ASD by age 10 years

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Summary

Introduction

Autism Spectrum disorder is one of the commonest and most important neurodevelopmental conditions affecting children today. In our well-characterised prospective cohort of autistic children, we confirmed mid-gestational alterations in maternal IL-4 concentrations in autism affected pregnancies versus matched controls. These findings add to promising evidence from animal models and retrospective screening programmes and adds to the knowledge in this field. Some authors have found that specific HLA-DR (Human leukocyte antigen) subtypes are overexpressed in children with ASD versus ­controls[12,13] Despite these advances, we are yet to discover a single gene determinant that can account for more than a small percent of ASD cases. The current ASD literature suggests that mutations occurring in genes involved in synapse formation, cell adhesion molecule production (such as Cadherins), scaffolding proteins (SHANK proteins), ion channels (sodium, calcium, and potassium channels), and signaling molecules can disrupt regulatory or coding regions and affect synapse formation, plasticity and synaptic ­transmission[16]

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