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dc.contributor.authorAlayli, Gamze
dc.contributor.authorAydin, Fatma
dc.contributor.authorCoban, Ahmet Yilmaz
dc.contributor.authorSuellue, Yueksel
dc.contributor.authorCantuerk, Ferhan
dc.contributor.authorBek, Yueksel
dc.contributor.authorCantuerk, Tayyar
dc.date.accessioned2020-06-21T15:19:18Z
dc.date.available2020-06-21T15:19:18Z
dc.date.issued2007
dc.identifier.issn0770-3198
dc.identifier.issn1434-9949
dc.identifier.urihttps://doi.org/10.1007/s10067-006-0503-z
dc.identifier.urihttps://hdl.handle.net/20.500.12712/19847
dc.descriptionWOS: 000247783800015en_US
dc.descriptionPubMed: 17211678en_US
dc.description.abstractThe pathogenesis of Behcet's disease (BD) is not fully understood and immunological abnormalities and genetic factors have been investigated. Because serum concentrations of mainly T helper 1 (Th1) type cells have been reported to be increased in BD, we aimed to investigate whether certain cytokine polymorphisms might represent a risk factor for developing BD. We genotyped 80 patients with BD and 105 healthy controls for interleukin (IL)-1 alpha (T/C -889), IL-1 beta (C/T -511, T/C +3962), IL-1R (C/T pst11970), IL-1RA (T/C mspa111100), IL-2 (T/G -330), IL-12 (C/A -1188), interferon (IFN)-gamma (A/T UTR 5644), and TNF-alpha (G/A -238) polymorphisms. Analyses of cytokine polymorphisms were performed with PCR-SSP. The genotype and allele frequencies of the patients and controls were compared and the association between the polymorphisms of the cytokines with the clinical findings was investigated. Genotype distribution showed significant differences between the patients and the controls for the IL-1 alpha -889, IL-1 beta -511, IL-1 beta +3962, IL-1R, IL-12, IFN- gamma, and TNF-alpha cytokines. We didn't observe significant difference in genotypic frequencies of IL-1RA and IL-2 in our study. Comparison of the IL-1 alpha -889, IL 1 beta -511, and IL 1 beta +3962 genotype frequencies showed significant increase in CC genotype between the patients and the controls. The individuals with IL-1R TT polymorphism had a higher risk for BD compared to patients with CT/CC polymorphism. Comparison of IL-12, IFN- gamma, and TNF-alpha, genotype frequencies showed significant increase in CA, AA, and AA genotypes between the patients and controls, respectively. The frequencies of genotypes according to the clinical features of the patients with BD did not show a significant difference (p > 0.05). Our study suggests that development of BD might be determined by various cytokine gene polymorphisms. However, further studies on larger numbers of cases are needed before definite conclusions can be drawn.en_US
dc.language.isoengen_US
dc.publisherSpringer London Ltden_US
dc.relation.isversionof10.1007/s10067-006-0503-zen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBehcet's diseaseen_US
dc.subjectcytokineen_US
dc.subjectgeneen_US
dc.subjectpolymorphismen_US
dc.titleT helper 1 type cytokines polymorphisms: association with susceptibility to Behcet's diseaseen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume26en_US
dc.identifier.issue8en_US
dc.identifier.startpage1299en_US
dc.identifier.endpage1305en_US
dc.relation.journalClinical Rheumatologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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