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dc.contributor.authorKucukali, I
dc.contributor.authorSazci, A
dc.contributor.authorErgul, E
dc.contributor.authorKara, I
dc.contributor.authorKaya, G
dc.date.accessioned2021-03-05T14:52:17Z
dc.date.available2021-03-05T14:52:17Z
dc.date.issued2005
dc.identifier.citationSazci A., Ergul E., Kucukali I., Kara I., Kaya G., "Association of the C677T and A1298C polymorphisms of methylenetetrahydrofolate reductase gene with schizophrenia: Association is significant in men but not in women", PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY, cilt.29, ss.1113-1123, 2005
dc.identifier.issn0278-5846
dc.identifier.othervv_1032021
dc.identifier.otherav_b93da3fc-e142-4869-80e6-6933eb3ac102
dc.identifier.urihttp://hdl.handle.net/20.500.12627/123256
dc.identifier.urihttps://doi.org/10.1016/j.pnpbp.2005.06.022
dc.description.abstractSchizophrenia is a complex and common psychiatric disorder with a polygenic inheritance. In our previous report, we showed an association between the methylenetetrahydro to I ate reductase (MTHFR) gene C677T and A1298C polymorphisms and schizophrenia in patients from Bakirkoy in Istanbul, Turkey [Sazci, A., Ergul, E., Guzelhan, Y., Kaya, G., Kara, I., 2003. Methylenetetrahydrofolate reductase gene polymorphisms in patients with schizophrenia. Mol. Brain Res. 117, 104-107]. We wanted also independently to confirm this study in a gender-specific manner with schizophrenic patients from Erenkoy in Istanbul, Turkey. To investigate the role of the C677T and A1298C polymorphisms of methylenetetrahydrofolate reductase gene in schizophrenia in a gender-specific manner, we analyzed the genotypes of MTHFR677 and MTHFR1298 of 297 schizophrenic patients and 341 healthy controls, using a polymerase chain reaction restriction fragment length polymorphism method. The MTHFR 677T allele was significantly distributed (x(2)=7.3121- P=0.026), between schizophrenic patients and healthy controls. The T677T genotype was overrepresented in the total schizophrenic patients (OR=1.938; 95%CI=1.133-3.315; x(2)=5.996; P=0.014). Similarly, the T677T/AI298A compound genotype was the most significant one in the total schizophrenic patients (OR=2.397; 95% CI=1.327-4.330; x(2) =8.821; P=0.003). The C1298C genotype was overrepresented in the total schizophrenic patients (OR= 1.706; 95%CI=1.014-2.870; x(2) =4.126; P=0.042). Likewise, the C677C/CI298C compound genotype was significant in the total schizophrenic patients (OR=1.689; 95%CI=0.985-2.894; x(2) =3.695; P=0.055). When schizophrenic patients and healthy controls were stratified according to gender difference, the T677T genotype and T677T/AI298A compound genotype were significantly overrepresented (OR-2.184; 95%CI=1.069-4.462; x(2) =4.767; P=0.029; OR=2.748; 95%CI=1.215-6.214; x(2) =6.301; P=0.012, respectively) in men schizophrenic patients. However, neither the MTHFR C677T nor the A I 298C polymorphisms are associated with schizophrenia in women. In conclusion, the MTHFR 677T allele and T677T, C1298C genotypes, and T677T/AI298A, C677C/CI298C compound genotypes are genetic risk factors for schizophrenia in men but not in women in a gender-specific manner. (c) 2005 Elsevier Inc. All rights reserved.
dc.language.isoeng
dc.subjectEczacılık
dc.subjectKLİNİK NEUROLOJİ
dc.subjectTemel Eczacılık Bilimleri
dc.subjectYaşam Bilimleri
dc.subjectTemel Bilimler
dc.subjectSinirbilim ve Davranış
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectFARMAKOLOJİ VE ECZACILIK
dc.subjectFarmakoloji ve Toksikoloji
dc.subjectPsikiyatri
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectNöroloji
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectNEUROSCIENCES
dc.titleAssociation of the C677T and A1298C polymorphisms of methylenetetrahydrofolate reductase gene with schizophrenia: Association is significant in men but not in women
dc.typeMakale
dc.relation.journalPROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY
dc.contributor.department, ,
dc.identifier.volume29
dc.identifier.issue7
dc.identifier.startpage1113
dc.identifier.endpage1123
dc.contributor.firstauthorID38455


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