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dc.creatorMandić-Maravić, Vanja
dc.creatorCorić, Vesna
dc.creatorMitkovic-Voncina, Marija
dc.creatorĐorđević, Miroslav L.
dc.creatorSavic-Radojević, Ana
dc.creatorErcegovac, Marko
dc.creatorMatić, Marija
dc.creatorSimić, Tatjana
dc.creatorLečić-Toševski, Dušica
dc.creatorTošković, Oliver
dc.creatorPekmezović, Tatjana
dc.creatorPljesa-Ercegovac, Marija
dc.creatorPejović-Milovančević, Milica
dc.date.accessioned2021-10-12T13:01:54Z
dc.date.available2021-10-12T13:01:54Z
dc.date.issued2019
dc.identifier.issn2045-2322
dc.identifier.urihttp://reff.f.bg.ac.rs/handle/123456789/2846
dc.description.abstractAutism spectrum disorders (ASD) are a group of complex psychiatric disorders, with a proposed gene-environment interaction in their etiology. One mechanism that could explain both the genetic and environmental component is oxidative stress. The aim of our study was to investigate the potential role of common polymorphisms in genes for glutathione transferase A1, M1, T1 and P1 in susceptibility to ASD. We also aimed to explore the possible oxidative stress - specific gene-environment interaction, regarding GST polymorphisms, maternal smoking tobacco during pregnancy (TSDP) and the risk of ASD. This case-control study included 113 children with ASD and 114 age and sex-matched controls. The diagnosis was made based on ICD-10 criteria and verified by Autism Diagnostic Interview - Revised (ADI-R). We investigated GSTA1, GSTM1, GSTP1 and GSTT1 genotypes and explored their individual and combined effects in individuals with ASD. Individual effect of GST genotypes was shown for GSTM1 active genotype decreasing the risk of ASD (OR = 0.554, 95% CI: 0.313-0.983, p = 0.044), and for GSTA1 CC genotype, increasing susceptibility to ASD (OR = 4.132, 95% CI: 1.219-14.012, p = 0.023); the significance was lost when genotype-genotype interactions were added into the logistic regression model. The combination of GSTM1 active and GSTT1 active genotype decreased the risk of ASD (OR = 0.126, 95% CI: 0.029-0.547, p = 0.006), as well as combination of GSTT1 active and GSTP1 llelle (OR = 0.170, 95% CI: 0.029-0.992, p = 0.049). Increased risk of ASD was observed if combination of GSTM1 active and GSTP1 llelle was present (OR = 11.088, 95% CI: 1.745-70.456, p = 0.011). The effect of TSDP was not significant for the risk of ASD, neither individually, nor in interaction with specific GST genotypes. Specific combination of GST genotypes might be associated with susceptibility to ASD, while it appears that maternal smoking during pregnancy does not increase the risk of ASD.en
dc.publisherNature Publishing Group, London
dc.relationinfo:eu-repo/grantAgreement/EC/FP7/223423/EU//
dc.relationinfo:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/175052/RS//
dc.rightsopenAccess
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceScientific Reports
dc.titleInteraction of glutathione S-transferase polymorphisms and tobacco smoking during pregnancy in susceptibility to autism spectrum disordersen
dc.typearticle
dc.rights.licenseBY
dc.citation.other9: -
dc.citation.rankM21
dc.citation.volume9
dc.identifier.doi10.1038/s41598-019-39885-w
dc.identifier.fulltexthttp://reff.f.bg.ac.rs/bitstream/id/1518/2843.pdf
dc.identifier.pmid30824761
dc.identifier.scopus2-s2.0-85062401685
dc.identifier.wos000459983900012
dc.type.versionpublishedVersion


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