Abstract

BackgroundSeveral studies pointed to immune dysregulation abnormalities linked to autism spectrum disorders (ASD). Of those, several autoantibodies had been identified. Recent findings of N-methyl d-aspartate (NMDA) antibodies in autoimmune encephalitis suggested that it caused symptoms like autistic regression. Thus, the purpose of the study was to test for the presence of anti-NMDAR antibodies in the ASD disorder population and to correlate this with the clinical findings.ResultsEighty-seven autistic children, 4–12 years old, were enrolled in the study and were matched with sixty typically developing children used as controls. The diagnosis of cases was confirmed by ADOS-2 and clinical evaluation. None of the control children had positive anti-NMDAR antibodies, while 26.4% (23 children) of the patients’ group were positive for serum anti-NMDA receptor antibodies (> 200 pg/ml, p = 0.0157). The positive anti-NMDAR antibody was statistically correlated with better speech stage (p = 0.017), more severe stereotyped behavior (p ≤ 0.001), and abnormal EEG findings (p = 0.025).ConclusionsThere is a possibility of the presence of anti-NMDAR antibodies in the autism spectrum disorder population with certain characteristics, especially the severity of the stereotyped behaviors.

Highlights

  • Several studies pointed to immune dysregulation abnormalities linked to autism spectrum disorders (ASD)

  • The study included eighty-seven children with ASD compared to sixty normal healthy controls

  • The mean age of the patient population in the study was 80.53 +\− 29.71 months old. This was matched to the mean age of the control group which was 79.45 +\− 29.95 months old (t = 2.944, p = 0.568)

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Summary

Introduction

Several studies pointed to immune dysregulation abnormalities linked to autism spectrum disorders (ASD). The purpose of the study was to test for the presence of anti-NMDAR antibodies in the ASD disorder population and to correlate this with the clinical findings. Autism spectrum disorder (ASD) is a pervasive developmental disorder characterized by impairment in communication and reciprocal social interaction, as well as stereotypic/repetitive behaviors. About 10–20% of autism cases can be attributed to evident genetic causes, yet incomplete concordance rates for monozygotic twins and phenotypical variabilities. ASD has been linked to immunological dysregulation on many levels. Several studies have found an increased incidence of immunological disorders in children with ASD [18]. Some studies pointed out to associations between immune system abnormalities or cytokine aberrations with ASD [21]. Evidence included upregulation of inflammation markers [27]

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