Investigation of the Relation between Epithelial Barrier Function and Autism Symptom Severity in Children with Autism

Kevser Nalbant1, Semih Erden2, Abdullah Yazar3

  • 1Medical Faculty, Department of Child and Adolescent Psychiatry, Hacettepe University, Ankara, Turkey. drkevser@yahoo.com.

Insights

Children with autism spectrum disorder (ASD) show lower levels of the protein occludin, indicating impaired epithelial barrier function. This finding may help understand ASD

Area of Science:

  • Neurobiology
  • Gastroenterology
  • Developmental Pediatrics

Background:

  • Autism spectrum disorder (ASD) is a neurodevelopmental condition marked by social communication deficits and repetitive behaviors.
  • Biological underpinnings of ASD, including epithelial barrier function, are areas of active research.
  • Altered gut-brain axis signaling is increasingly implicated in ASD pathogenesis.

Purpose of the Study:

  • To investigate epithelial barrier function in children with ASD.
  • To compare serum levels of occludin and zonulin between children with ASD and neurotypical controls.
  • To explore the association between epithelial barrier markers and ASD symptom severity.

Main Methods:

  • A case-control study involving 60 children with ASD and 30 controls.
  • Serum occludin and zonulin concentrations were measured using enzyme-linked immunosorbent assay (ELISA).
  • Autism symptom severity was assessed using the Childhood Autism Rating Scale (CARS).

Main Results:

  • Children with ASD exhibited significantly lower serum occludin levels compared to controls.
  • Reduced occludin levels in ASD were significantly correlated with higher CARS total scores.
  • Zonulin levels were not significantly different between the groups (data not shown in abstract).

Conclusions:

  • Children with ASD demonstrate compromised epithelial barrier function, evidenced by decreased serum occludin.
  • Occludin levels may serve as a potential biomarker for ASD symptom severity.
  • Further research into the mechanisms of occludin dysregulation is crucial for understanding ASD etiology and treatment.

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