dc.contributor.author | Pehlivan, Sacide | |
dc.contributor.author | Uysal, Metin Atilla | |
dc.contributor.author | Aydın, Nazan | |
dc.contributor.author | Nursal, Ayşe Feyda | |
dc.contributor.author | Pehlivan, Mustafa | |
dc.contributor.author | Yavuzlar, Hazal | |
dc.contributor.author | Sever, Ülgen | |
dc.contributor.author | Kurnaz, Selin | |
dc.contributor.author | Yavuz, Fatih Kasım | |
dc.contributor.author | Uysal, Suna | |
dc.contributor.author | Çetinay Aydın, Pınar | |
dc.date.accessioned | 2019-05-10T09:39:25Z | |
dc.date.available | 2019-05-10T09:39:25Z | |
dc.date.issued | 2018 | |
dc.identifier.citation | Pehlivan, 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.issn | 0101-6083 | |
dc.identifier.issn | 1806-938X | |
dc.identifier.uri | https://doi.org/10.1590/0101-60830000000157 | |
dc.identifier.uri | https://hdl.handle.net/11491/690 | |
dc.description.abstract | Background: 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.iso | eng | |
dc.publisher | Universidade de Sao Paulo | en_US |
dc.relation.isversionof | 10.1590/0101-60830000000157 | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0/legalcode | * |
dc.subject | DNA Repair | en_US |
dc.subject | Nicotine Dependence | en_US |
dc.subject | Schizophrenia | en_US |
dc.subject | XRCC4 | en_US |
dc.title | XRCC4 rs6869366 polymorphism is associated with susceptibility to both nicotine dependence and/or schizophrenia | en_US |
dc.type | article | en_US |
dc.relation.journal | Archives of Clinical Psychiatry | en_US |
dc.department | Hitit Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü | en_US |
dc.authorid | 0000-0001-7639-1122 | en_US |
dc.identifier.volume | 45 | en_US |
dc.identifier.issue | 3 | en_US |
dc.identifier.startpage | 53 | en_US |
dc.identifier.endpage | 56 | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |