Macrophage migration inhibitory factor -173GC variant might increase the risk of behçet's disease
dc.authorid | 0000-0001-7639-1122 | |
dc.contributor.author | Nursal, Ayşe Feyda | |
dc.contributor.author | Yiğit, Serbülent | |
dc.contributor.author | Tural, Ercan | |
dc.contributor.author | Kalkan, Göknur | |
dc.contributor.author | Tümer, Mehmet Kemal | |
dc.contributor.author | Tekcan, Akın | |
dc.date.accessioned | 2019-05-13T08:58:37Z | |
dc.date.available | 2019-05-13T08:58:37Z | |
dc.date.issued | 2018 | |
dc.department | Hitit Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü | |
dc.description.abstract | Objective: The aim of the present study was to investigate any possible association between the macrophage migration inhibitory factor (MIF) -173GC variant and Behçet's disease (BD) in a group of Turkish patients. Subjects and Methods: A total of 111 patients with BD and 100 healthy controls were enrolled in this study. Genomic DNA was extracted from peripheral lymphocytes. The MIF -173GC variant was genotyped using polymerase chain reaction restriction fragment length polymorphism. The allele and genotype frequencies of patients and controls were compared using the ?2 test. Results: A statistically significant difference in the distribution of the genotype was observed between BD patients and healthy controls. The homo-genotype CC was more prevalent in the patient group compared to the control group (p = 0.008, OR: 0.24, 95% Cl: 0.05-0.78). A significant association was observed when the patients were compared with the controls according to GG + GC versus CC ge-notypes (p = 0.003, OR: 1.21, 95% CI: 0.06-0.063). Allele frequencies of the MIF -173GC variant did not show any statistically significant difference between patients and controls. Conclusion: In this study, we conclude that the CC ge-notype of the MIF -173GC variant may be a risk factor in the pathogenesis of BD in the Turkish population. However, further studies with larger samples are needed to address the exact role of this variant in BD. © 2018 The Author(s) Published by S. Karger AG, Basel. | |
dc.identifier.doi | 10.1159/000489340 | |
dc.identifier.endpage | 289 | en_US |
dc.identifier.issn | 1011-7571 | |
dc.identifier.issue | 3 | en_US |
dc.identifier.scopusquality | Q1 | |
dc.identifier.startpage | 285 | en_US |
dc.identifier.uri | https://doi.org/10.1159/000489340 | |
dc.identifier.uri | https://hdl.handle.net/11491/1170 | |
dc.identifier.volume | 27 | en_US |
dc.identifier.wosquality | N/A | |
dc.indekslendigikaynak | Web of Science | |
dc.indekslendigikaynak | Scopus | |
dc.indekslendigikaynak | PubMed | |
dc.language.iso | en | |
dc.publisher | S. Karger AG | |
dc.relation.ispartof | Medical Principles and Practice | |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | |
dc.rights | Attribution-NonCommercial 4.0 International (CC BY-NC 4.0) | * |
dc.rights | info:eu-repo/semantics/openAccess | |
dc.rights.uri | https://creativecommons.org/licenses/by-nc/4.0/ | * |
dc.subject | Behçet’s Disease | en_US |
dc.subject | Macrophage Migration Inhibitory Factor | en_US |
dc.subject | Variant | en_US |
dc.title | Macrophage migration inhibitory factor -173GC variant might increase the risk of behçet's disease | |
dc.type | Article |
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