Publication:
Serum IL-33 Level and IL-33 Gene Polymorphisms in Behçet’s Disease

dc.contributor.authorKoca S.S.
dc.contributor.authorKara M.
dc.contributor.authorDeniz F.
dc.contributor.authorOzgen M.
dc.contributor.authorDemir C.F.
dc.contributor.authorIlhan N.
dc.contributor.authorIsik A.
dc.date.accessioned2020-06-21T09:43:19Z
dc.date.available2020-06-21T09:43:19Z
dc.date.issued2015
dc.departmentOMÜen_US
dc.department-tempKoca, S.S., Department of Rheumatology, Firat University, Tip Fakultesi, Romatoloji BD, Elazig, 23119, Turkey -- Kara, M., Department of Medical Genetics, Mugla Sitki Kocman University, Mugla, Turkey -- Deniz, F., Department of Internal Medicine, Firat University, Elazig, Turkey -- Ozgen, M., Department of Rheumatology, 19 Mayis University, Malatya, Turkey -- Demir, C.F., Department of Neurology, Firat University, Elazig, Turkey -- Ilhan, N., Department of Biochemistry, Firat University, Elazig, Turkey -- Isik, A., Department of Rheumatology, Firat University, Tip Fakultesi, Romatoloji BD, Elazig, 23119, Turkeyen_US
dc.description.abstractBehçet’s disease (BD) is a chronic inflammatory disease. Increased productions of cytokines including interleukin (IL)-1? and IL-18 are documented, and IL-1? and ? gene polymorphisms are associated with susceptibility to the disease. IL-33 is a recently discovered member of IL-1 cytokine family. The aim of the study was to detect serum IL-33 level and IL-33 gene polymorphisms in a cohort of BD. Unrelated 117 patients with BD and 149 healthy controls (HC) were enrolled. Serum IL-33 levels were analyzed by enzyme-linked immunosorbent assay method. DNA samples were harvested using an appropriate commercial DNA isolation kit. Four single nucleotide polymorphisms of IL-33 gene (rs7044343, rs1157505, rs11792633 and rs1929992) were genotyped using the appropriate commercial primer/probe sets on real-time PCR. Serum IL-33 level was not significantly different in the BD and HC groups (p > 0.05). However, its level was lower in the active BD patients compared to the inactive ones and HC group (p = 0.044 and p = 0.037, respectively). There was no significant difference in terms of the genotypic and allelic distributions of rs1157505 and rs1929992 polymorphisms (p > 0.05 for all). However, the TT variants of rs7044343 and rs11792633 polymorphisms were very rare, and the T allele frequencies of these polymorphisms were lower, in the BD group compared to the HC group (p < 0.0001 for all). The rs7044343 and rs11792633 variants of IL-33 gene are associated with the decreased risk of BD in our cohort. Therefore, it may be concluded that IL-33 acts a protective role on the pathogenesis of BD. © 2014, Springer-Verlag Berlin Heidelberg.en_US
dc.identifier.doi10.1007/s00296-014-3111-2
dc.identifier.endpage477en_US
dc.identifier.issn0172-8172
dc.identifier.issue3en_US
dc.identifier.pmid25119832
dc.identifier.startpage471en_US
dc.identifier.urihttps://doi.org/10.1007/s00296-014-3111-2
dc.identifier.urihttps://hdl.handle.net/20.500.12712/5299
dc.identifier.volume35en_US
dc.language.isoenen_US
dc.publisherSpringer Verlagen_US
dc.relation.journalRheumatology Internationalen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBehçet’s Diseaseen_US
dc.subjectIL-33en_US
dc.subjectPolymorphismsen_US
dc.titleSerum IL-33 Level and IL-33 Gene Polymorphisms in Behçet’s Diseaseen_US
dc.typeArticleen_US
dspace.entity.typePublication

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