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Associations between polymorphisms of IL-17F and IL-17A genes with disease activity and clinical outcome of Ankylosing Spondylitis

dc.contributor.authorİnal, Erkol Esra
dc.contributor.authorEroğlu, Selma
dc.contributor.authorSolak, Özlem
dc.contributor.authorGörükmez, Özlem
dc.contributor.buuauthorSağ, Özemri
dc.contributor.buuauthorGörukmez, Orhan
dc.contributor.buuauthorYakut, Tahsin
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentTıbbi Genetik Ana Bilim Dalı
dc.contributor.researcheridAFZ-0764-2022
dc.contributor.scopusid56681045900
dc.contributor.scopusid56879109500
dc.contributor.scopusid6602802424
dc.date.accessioned2023-04-14T06:29:42Z
dc.date.available2023-04-14T06:29:42Z
dc.date.issued2016
dc.description.abstractAims: In this study, we aimed to investigate the associations between the 7383A/G and 7488A/G polymorphisms of the interleukin (IL)-17F gene and the G197A polymorphism of the IL-17A gene with disease activity and clinical outcomes in Turkish patients with ankylosing spondylitis (AS). Methods: The study included 101 AS patients and 106 healthy controls. The erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP) levels, in addition to scores of the Bath Ankylosing Spondylitis Disease Activity Index, Bath Ankylosing Spondylitis Metrology Index and Bath Ankylosing Spondylitis Functional Index (BASFI) of the patients, were recorded. The frequencies of genotypes 7383A/G and 7488A/G of the IL-17F and G197A of IL-17A genes and alleles were compared between the patients and healthy controls. Results: There were significant differences in the allele frequencies and genotype distribution of IL-17F 7488A/G. There were also significant differences in the CRP levels and BASFI scores of patients due to the genotype distribution of the IL-17F 7488A/G polymorphism (p=0.029, 0.045, respectively). Conclusions: This study suggests that the IL-17F 7488A/G polymorphism may be associated with susceptibility to AS, disease activity and functional status in Turkish patients. Further studies with larger numbers of AS patients, with a long-term follow-up, are needed to elucidate the observed relations.
dc.identifier.citationİnal, E. vd. (2016). "Associations between polymorphisms of IL-17F and IL-17A genes with disease activity and clinical outcome of Ankylosing Spondylitis". Acta Reumatologica Portuguesa, 41(3), 232-239.
dc.identifier.endpage239
dc.identifier.issn0303-464X
dc.identifier.issue3
dc.identifier.pubmed27155445
dc.identifier.scopus2-s2.0-84994130063
dc.identifier.startpage232
dc.identifier.urihttp://hdl.handle.net/11452/32383
dc.identifier.volume41
dc.identifier.wos000386550800007
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherPublisaude-Edicoes Medicas
dc.relation.collaborationYurt içi
dc.relation.collaborationSanayi
dc.relation.journalActa Reumatologica Portuguesa
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectRheumatology
dc.subjectAnkylosing spondylitis
dc.subject7383 A/G
dc.subject7488 A/G
dc.subjectG197A
dc.subjectIL-17 gene
dc.subjectInterleukin-17f genes
dc.subjectT-cell
dc.subjectSusceptibility
dc.subjectIL17F
dc.subjectReliability
dc.subjectSeverity
dc.subjectT(h)17
dc.subjectErap1
dc.subjectIL23R
dc.subject.emtreeIL17A protein, human
dc.subject.emtreeIL17F protein, human
dc.subject.emtreeInterleukin 17
dc.subject.emtreeAdult
dc.subject.emtreeCross-sectional study
dc.subject.emtreeFemale
dc.subject.emtreeGenetic polymorphism
dc.subject.emtreeGenetics
dc.subject.emtreeHuman
dc.subject.emtreeMale
dc.subject.emtreeSpondylitis, ankylosing
dc.subject.meshAdult
dc.subject.meshCross-sectional studies
dc.subject.meshFemale
dc.subject.meshHumans
dc.subject.meshInterleukin-17
dc.subject.meshMale
dc.subject.meshPolymorphism, genetic
dc.subject.meshSpondylitis, ankylosing
dc.subject.scopusSpondylarthritis; Aminopeptidases; Ankylosing Spondylitis
dc.subject.wosRheumatology
dc.titleAssociations between polymorphisms of IL-17F and IL-17A genes with disease activity and clinical outcome of Ankylosing Spondylitis
dc.typeArticle
dc.wos.quartileQ4
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Tıbbi Genetik Ana Bilim Dalı
local.indexed.atScopus
local.indexed.atWOS

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