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
Institute of Mental Health, Belgrade, Serbia.
Faculty of Medicine, University of Belgrade, Belgrade, Serbia.
Front Psychiatry. 2019 Sep 25;10:675. doi: 10.3389/fpsyt.2019.00675. eCollection 2019.
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. 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. 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 , as opposed to carriers of genotype. Specific perinatal complications may be significant risk factors for ASD. 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.
自闭症谱系障碍(ASD)是复杂的精神疾病,其病因基于基因与环境的相互作用。围产期并发症与ASD之间的关联已得到充分证实。最近的研究结果表明,氧化应激和编码抗氧化酶的基因多态性可能与ASD的发生发展有关。谷胱甘肽转移酶(GSTs)在抗氧化防御系统中起重要作用。我们旨在确定产前和围产期并发症(作为可能的氧化应激诱导因素)对ASD风险的预测作用是否依赖于GST基因多态性。该研究纳入了113例ASD病例和114例年龄及性别匹配的健康对照。对所有参与者进行了GSTA1、GSTM1、GSTT1和GSTP1基因多态性的基因分型。对研究中的所有受试者进行了关于产前和围产期危险因素及并发症的问卷调查。作为一个整体评估的围产期并发症显著增加了ASD的风险[比值比(OR)=9.415;p=0.000],以及个体围产期并发症,如早产(OR=11.42;p=0.001)、新生儿黄疸(OR=8.774;p=0.000)、呼吸窘迫综合征(OR=4.835;p=0.047)以及孕期使用任何药物(OR=2.413;p=0.03)。在逻辑回归模型中,添加GST基因型并没有改变早产和新生儿黄疸作为ASD危险因素所发现的显著影响。然而,GST基因型与孕期用药和孕期使用宫缩抑制剂之间存在显著的相互作用,这仅在 基因型携带者中预测ASD风险,而在 基因型携带者中则不然。特定的围产期并发症可能是ASD的重要危险因素。 基因型可能作为某些产前因素对ASD风险影响的调节因子,如孕期用药。可以推测,不同的氧化应激相关遗传和环境因素可能导致ASD的发生。除了病因机制外,还讨论了ASD可能的治疗意义。