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Autism Spectrum Disorders and Perinatal Complications—Is Oxidative Stress the Connection?

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 enc...

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Autores principales: Mandic-Maravic, Vanja, Mitkovic-Voncina, Marija, Pljesa-Ercegovac, Marija, Savic-Radojevic, Ana, Djordjevic, Miroslav, Pekmezovic, Tatjana, Grujicic, Roberto, Ercegovac, Marko, Simic, Tatjana, Lecic-Tosevski, Dusica, Pejovic-Milovancevic, Milica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6798050/
https://www.ncbi.nlm.nih.gov/pubmed/31681027
http://dx.doi.org/10.3389/fpsyt.2019.00675
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author Mandic-Maravic, Vanja
Mitkovic-Voncina, Marija
Pljesa-Ercegovac, Marija
Savic-Radojevic, Ana
Djordjevic, Miroslav
Pekmezovic, Tatjana
Grujicic, Roberto
Ercegovac, Marko
Simic, Tatjana
Lecic-Tosevski, Dusica
Pejovic-Milovancevic, Milica
author_facet Mandic-Maravic, Vanja
Mitkovic-Voncina, Marija
Pljesa-Ercegovac, Marija
Savic-Radojevic, Ana
Djordjevic, Miroslav
Pekmezovic, Tatjana
Grujicic, Roberto
Ercegovac, Marko
Simic, Tatjana
Lecic-Tosevski, Dusica
Pejovic-Milovancevic, Milica
author_sort Mandic-Maravic, Vanja
collection PubMed
description 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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spelling pubmed-67980502019-11-01 Autism Spectrum Disorders and Perinatal Complications—Is Oxidative Stress the Connection? Mandic-Maravic, Vanja Mitkovic-Voncina, Marija Pljesa-Ercegovac, Marija Savic-Radojevic, Ana Djordjevic, Miroslav Pekmezovic, Tatjana Grujicic, Roberto Ercegovac, Marko Simic, Tatjana Lecic-Tosevski, Dusica Pejovic-Milovancevic, Milica Front Psychiatry Psychiatry 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. Frontiers Media S.A. 2019-09-25 /pmc/articles/PMC6798050/ /pubmed/31681027 http://dx.doi.org/10.3389/fpsyt.2019.00675 Text en Copyright © 2019 Mandic-Maravic, Mitkovic-Voncina, Pljesa-Ercegovac, Savic-Radojevic, Djordjevic, Pekmezovic, Grujicic, Ercegovac, Simic, Lecic-Tosevski and Pejovic-Milovancevic http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Psychiatry
Mandic-Maravic, Vanja
Mitkovic-Voncina, Marija
Pljesa-Ercegovac, Marija
Savic-Radojevic, Ana
Djordjevic, Miroslav
Pekmezovic, Tatjana
Grujicic, Roberto
Ercegovac, Marko
Simic, Tatjana
Lecic-Tosevski, Dusica
Pejovic-Milovancevic, Milica
Autism Spectrum Disorders and Perinatal Complications—Is Oxidative Stress the Connection?
title Autism Spectrum Disorders and Perinatal Complications—Is Oxidative Stress the Connection?
title_full Autism Spectrum Disorders and Perinatal Complications—Is Oxidative Stress the Connection?
title_fullStr Autism Spectrum Disorders and Perinatal Complications—Is Oxidative Stress the Connection?
title_full_unstemmed Autism Spectrum Disorders and Perinatal Complications—Is Oxidative Stress the Connection?
title_short Autism Spectrum Disorders and Perinatal Complications—Is Oxidative Stress the Connection?
title_sort autism spectrum disorders and perinatal complications—is oxidative stress the connection?
topic Psychiatry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6798050/
https://www.ncbi.nlm.nih.gov/pubmed/31681027
http://dx.doi.org/10.3389/fpsyt.2019.00675
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