Inanir Ahmet, Tural Sengul, Yigit Serbulent, Kalkan Goknur, Pancar Gunseli Sefika, Demir Helin Deniz, Ates Omer
Gaziosmanpaşa University, Faculty of Medicine, Department of Physical Medicine and Rehabilitation, Tokat, Turkey.
Mol Vis. 2013;19:675-83. Epub 2013 Mar 21.
Behçet's disease (BD) is a systemic vasculitis characterized by inflammatory lesions of the urogenital mucosa, eyes, skin, central nervous system, and joints. Vein thrombosis constitutes the most frequent vascular manifestation of the disease, and may cause such ocular vascular thrombotic events as central retinal vein and central retinal artery thrombosis. Thrombosis is a serious problem, and often leads to irreversible vision loss. Previous studies have shown that genetic factors predispose individuals to BD. Several cytokine genes might play crucial roles in host susceptibility to BD and to thrombophilia. Various polymorphic regions of the interleukin-4 (IL-4) gene (-1098G and 590T) are associated with BD in the Turkish population. This study was conducted in Turkish patients with BD to determine the frequency of the IL-4 gene 70 bp variable number of tandem repeats (VNTR) variant, and its association with clinical findings.
Genomic DNA obtained from 488 individuals (238 patients with Behçet's disease and 250 healthy controls) was used in the study. Genomic DNA was isolated and genotyped using PCR assay for the IL-4 gene 70 bp VNTR polymorphism determined by using PCR with the specific primers.
There was statistical significance between the groups regarding IL-4 genotype distribution (p<0.001, odds ratio: 2.55 [1.629-4.052], 95% confidence interval) and allele frequencies (p<0.0012.381[1.586-3.617], 95% confidence interval). When we examined IL-4 genotype frequencies according to the clinical characteristics, we observed a statistically significant association between the P₂P₂ genotype and deep venous thrombosis (p=0.01). Deep venous thrombosis was also associated with ocular involvement in our study group (p=0.014).
Our findings suggest that the IL-4 gene 70 bp VNTR polymorphism is associated with susceptibility to development of BD. Deep venous thrombosis is also associated with ocular involvement in BD. The IL-4 gene could be a genetic biomarker in Behçet's disease in a Turkish study population.
白塞病(BD)是一种全身性血管炎,其特征为泌尿生殖黏膜、眼睛、皮肤、中枢神经系统和关节出现炎症性病变。静脉血栓形成是该病最常见的血管表现,可能导致诸如视网膜中央静脉和视网膜中央动脉血栓形成等眼部血管血栓事件。血栓形成是一个严重问题,常导致不可逆的视力丧失。既往研究表明,遗传因素使个体易患白塞病。几种细胞因子基因可能在宿主对白塞病和血栓形成倾向的易感性中起关键作用。白细胞介素-4(IL-4)基因的各种多态性区域(-1098G和590T)与土耳其人群中的白塞病相关。本研究在土耳其白塞病患者中进行,以确定IL-4基因70 bp可变数目串联重复序列(VNTR)变异的频率及其与临床发现的关联。
本研究使用了从488名个体(238例白塞病患者和250名健康对照)获得的基因组DNA。分离基因组DNA,并使用针对IL-4基因70 bp VNTR多态性的PCR检测进行基因分型,该多态性通过使用特异性引物进行PCR确定。
两组在IL-4基因型分布(p<0.001;优势比:2.55 [1.629 - 4.052],95%置信区间)和等位基因频率(p<0.001;2.381 [1.586 - 3.617],95%置信区间)方面存在统计学意义。当我们根据临床特征检查IL-4基因型频率时,我们观察到P₂P₂基因型与深静脉血栓形成之间存在统计学显著关联(p = 0.01)。在我们的研究组中,深静脉血栓形成也与眼部受累相关(p = 0.014)。
我们的研究结果表明,IL-4基因70 bp VNTR多态性与白塞病的易感性相关。深静脉血栓形成也与白塞病的眼部受累相关。在土耳其研究人群中,IL-4基因可能是白塞病的一种遗传生物标志物。