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dc.contributor.authorPehlivan, Sacide
dc.contributor.authorUysal, Metin Atilla
dc.contributor.authorAydın, Nazan
dc.contributor.authorNursal, Ayşe Feyda
dc.contributor.authorPehlivan, Mustafa
dc.contributor.authorYavuzlar, Hazal
dc.contributor.authorSever, Ülgen
dc.contributor.authorKurnaz, Selin
dc.contributor.authorYavuz, Fatih Kasım
dc.contributor.authorUysal, Suna
dc.contributor.authorÇetinay Aydın, Pınar
dc.date.accessioned2019-05-10T09:39:25Z
dc.date.available2019-05-10T09:39:25Z
dc.date.issued2018
dc.identifier.citationPehlivan, S., Uysal, M. A., Aydın, N., Nursal, A. F., Pehlivan, M., Yavuzlar, H., Sever, Ü., Yavuz, F. K., Uysal, S., Çetinay Aydın, P. (2018). XRCC4 rs6869366 polymorphism is associated with susceptibility to both nicotine dependence and/or schizophrenia. Archives of Clinical Psychiatry, 45(3), 53-56.en_US
dc.identifier.issn0101-6083
dc.identifier.issn1806-938X
dc.identifier.urihttps://doi.org/10.1590/0101-60830000000157
dc.identifier.urihttps://hdl.handle.net/11491/690
dc.description.abstractBackground: Oxidative stress induced DNA damage has been assumed to contribute to the etiopathogenesis of schizophrenia (Sch). Smoking prevalence was more common in patients with Sch. The X-ray repair cross-complementation group 4 (XRCC4) gene plays an important role in the repair of DNA double-strand breaks. Objective: The purpose of this study was to investigate whether XRCC4 rs6869366 polymorphism has a relationship both in nicotine dependence (ND) and Sch+ND risk. Methods: One hundred and four patients with Sch+ND, 133 subjects with ND only and 70 healthy controls were enrolled in the study. XRCC4 rs6869366 polymorphism was analyzed using PCR-RFLP assay. Results: The frequency of XRCC4 rs6869366 GG genotype was more common in the ND and Sch+ND group than controls (p = 0.001 and p = 0.001, respectively). XRCC4 rs6869366 TT genotype was lower in both ND and Sch+ND group compared to controls (p = 0.001 and p = 0.001, respectively). Also, XRCC4 rs6869366 G allele was higher in Sch+ND group than controls (p = 0.001) while XRCC4 rs6869366 T allele was lower in ND group than healthy controls (p=0.001). XRCC4 rs6869366 GT genotype was lower in ND group than control group (p = 0.003). Discussion: These results suggested that the XRCC4 rs6869366 polymorphism G related genotype/allele was associated with susceptibility to both ND and Sch+ND in a Turkish population. © 2018, Universidade de Sao Paulo. All rights reserved.en_US
dc.language.isoeng
dc.publisherUniversidade de Sao Pauloen_US
dc.relation.isversionof10.1590/0101-60830000000157en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/legalcode*
dc.subjectDNA Repairen_US
dc.subjectNicotine Dependenceen_US
dc.subjectSchizophreniaen_US
dc.subjectXRCC4en_US
dc.titleXRCC4 rs6869366 polymorphism is associated with susceptibility to both nicotine dependence and/or schizophreniaen_US
dc.typearticleen_US
dc.relation.journalArchives of Clinical Psychiatryen_US
dc.departmentHitit Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümüen_US
dc.authorid0000-0001-7639-1122en_US
dc.identifier.volume45en_US
dc.identifier.issue3en_US
dc.identifier.startpage53en_US
dc.identifier.endpage56en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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