4.7 Article

Mid-gestation cytokine profiles in mothers of children affected by autism spectrum disorder: a case-control study

Journal

SCIENTIFIC REPORTS
Volume 11, Issue 1, Pages -

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41598-021-01662-z

Keywords

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Funding

  1. National Children's Research Centre, Children's Hospital Ireland at Crumlin, Dublin, Ireland [D/19/1]
  2. Irish Research Council [GOIPG/2017/1350]
  3. Irish Research Council (IRC) [GOIPG/2017/1350] Funding Source: Irish Research Council (IRC)

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Autism Spectrum Disorder is a common neurodevelopmental condition affecting children. This study aimed to examine mid-gestational maternal serum cytokine profiles in relation to autism risk. The study found significant alterations in IL-4 concentrations in the maternal serum of autistic children compared to matched controls, adding to the growing body of evidence in this field.
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-gamma, IL-1 beta, IL-4, IL-6, IL-8, IL-17A, GMCSF and TNF alpha 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.

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