Abstract

Background: Autism spectrum disorders (ASD) are a heterogeneous group of developmental disorders, with different levels of symptoms, functioning, and comorbidities. Recent findings suggested that oxidative stress and genetic variability in glutathione S-transferases (GSTs) might increase the risk of ASD development. We aimed to determine whether GST polymorphisms influence the severity of symptoms as well as the cognitive and adaptive abilities in children with ASD.Methods: The sample included 113 ASD cases. All participants were genotyped for GSTA1, GSTM1, GSTT1, and GSTP1 polymorphisms. The clinical characteristics were determined with Autism Diagnostic Interview-Revised (ADI-R) in all of the participants. In non-verbal participants, we explored the adaptive functioning using the Vineland Adaptive Behavior Scale II, while in verbal participants, we used the Wechsler Abbreviated Scale of Intelligence (WASI).Results: It was shown that the GSTA1*CC genotype was a predictor of a lower non-verbal communication impairment as well as of a lower chance of having seizures during life. GSTM1-active genotype predicted a higher adaptive functioning. The predictive effect of GSTA1, GSTM1, and GSTT1 genotype was moderated by exposure during pregnancy (maternal smoking and medication). The GSTP1*IleIle genotype was significantly associated to a better cognitive functioning in children with ASD.Conclusion: Besides the complex gene-environment interaction for the specific risk of developing ASD, there is also a possible complexity of interactions between genetic and environmental factors influencing the level of symptoms and impairment in people with ASD. Detoxification and antioxidant enzymes, such as GSTA1, might contribute to the core of this complexity.

Highlights

  • Autism spectrum disorders (ASD) are a heterogeneous group of disorders with key clinical features being deficits in social communication and restricted, repetitive patterns of behavior, interest, or activities [1, 2]

  • The results have shown a significant effect of the GSTM1-active genotype in decreasing the risk of ASD and for the GSTA1∗CC genotype in increasing the susceptibility to ASD [8]

  • It was shown that the GSTA1∗CC genotype was a predictor of a lower ADIR diagnostic communication non-verbal (Bnv) score, as well as, of a lower chance of having seizures during life

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Summary

Introduction

Autism spectrum disorders (ASD) are a heterogeneous group of disorders with key clinical features being deficits in social communication and restricted, repetitive patterns of behavior, interest, or activities [1, 2]. Recent data have shown the possible role of redox imbalance and oxidative stress in ASD [6,7,8,9]. A number of studies so far have shown the possible connection between oxidative stress and ASD [13,14,15]. Glutathione Stransferases (GSTs) have a very important role in antioxidant defense mechanisms by performing the detoxification of xenobiotics and inactivation of a large number of endogenous oxidative stress products [16, 17]. Several studies have shown a possible role of GST polymorphisms in ASD development [8, 9, 20, 21]. Autism spectrum disorders (ASD) are a heterogeneous group of developmental disorders, with different levels of symptoms, functioning, and comorbidities.

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