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Autism Spectrum Disorders and Perinatal Complications-Is Oxidative Stress the Connection?
Vanja Mandic-Maravic1,2, Marija Mitkovic-Voncina1,2, Marija Pljesa-Ercegovac2,3
1Institute of Mental Health, Belgrade, Serbia.
Insights
Perinatal complications significantly increase autism risk. The GSTM1 gene genotype may modify how prenatal factors, like medication use, affect autism risk, suggesting a gene-environment interaction in ASD development.
Area of Science:
- Neuroscience
- Genetics
- Environmental Health
Background:
- Autism spectrum disorders (ASD) are complex neurodevelopmental conditions influenced by gene-environment interactions.
- Oxidative stress and genetic variations in antioxidant enzymes, such as glutathione transferases (GSTs), are implicated in ASD etiology.
- Perinatal complications are recognized risk factors for ASD, potentially inducing oxidative stress.
Purpose of the Study:
- To investigate the role of glutathione transferase (GST) gene polymorphisms in mediating the association between prenatal/perinatal complications and ASD risk.
- To determine if GST genotypes modify the predictive effect of specific perinatal complications on ASD development.
Main Methods:
- Genotyping of GSTA1, GSTM1, GSTT1, and GSTP1 polymorphisms in 113 ASD cases and 114 controls.
- Administration of questionnaires to collect data on prenatal and perinatal risk factors.
- Logistic regression analysis to assess the interaction between GST genotypes and perinatal factors in ASD risk.
Main Results:
- Perinatal complications as a group significantly elevated ASD risk (OR=9.415).
- Specific complications like prematurity (OR=11.42) and neonatal jaundice (OR=8.774) were strong predictors of ASD.
- A significant interaction was observed between GSTM1 genotype and medication/tocolytic use during pregnancy, influencing ASD risk in carriers of the GSTM1-null genotype.
Conclusions:
- Certain perinatal complications are significant risk factors for autism spectrum disorders.
- The GSTM1 genotype may act as a moderator for prenatal factors, such as medication use, in ASD risk.
- The findings suggest a complex interplay of oxidative stress-related genetic and environmental factors in ASD pathogenesis.
Abstract:
Background: Autism spectrum disorders (ASD) are complex psychiatric disorders, with gene environment interaction being in the basis of their etiology. The association of perinatal complications and ASD is well established. Recent findings suggested that oxidative stress and polymorphism in genes encoding antioxidant enzymes might be involved in the development of ASD. Glutathione transferases (GSTs) have an important role in the antioxidant defense system. We aimed to establish whether the predictive effects of prenatal and perinatal complications (as possible oxidative stress inducers) on ASD risk are dependent on GST polymorphisms. Methods: The study included 113 ASD cases and 114 age- and sex group-matched healthy controls. All participants were genotyped for GSTA1, GSTM1, GSTT1, and GSTP1 polymorphisms. The questionnaire regarding prenatal and perinatal risk factors and complications was administered for all the subjects in the study. Results: The evaluated perinatal complications as a group significantly increased the risk of ASD [odds ratio (OR) = 9.415; p = 0.000], as well as individual perinatal complications, such as prematurity (OR = 11.42; p = 0.001), neonatal jaundice (OR = 8.774; p = 0.000), respiratory distress syndrome (OR = 4.835; p = 0.047), and the use of any medication during pregnancy (OR = 2.413; p = 0.03). In logistic regression model, adding GST genotypes did not modify the significant effects found for prematurity and neonatal jaundice as risk factors in ASD. However, there was a significant interaction of GST genotype with medication use during pregnancy and the use of tocolytics during pregnancy, which was predictive of ASD risk only in carriers of GSTM1-null, as opposed to carriers of GSTM1-active genotype. Conclusion: Specific perinatal complications may be significant risk factors for ASD. GSTM1 genotype may serve as a moderator of the effect of some prenatal factors on the risk of ASD such as using medication during pregnancy. It may be speculated that different oxidative stress-related genetic and environmental factors could lead to development of ASD. Apart from etiological mechanisms, possible therapeutic implications in ASD are also discussed.
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