Interleukin-27 gene variant rs153109 is associated with enhanced cytokine serum levels and susceptibility to Behçet's disease in the Iranian population.

IF 2.2 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Nasser Gholijani, Gholamreza Daryabor, Kurosh Kalantar, Mohammad-Reza Yazdani, Saeedeh Shenavandeh, Maryam Zahed, Zahra Jafarpour, Mohammad-Reza Malekmakan, Zahra Amirghofran
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引用次数: 7

Abstract

Behcet's disease (BD) is a systemic vasculitis, characterized by recurrent oral aphthous, genital ulcers, ocular lesions, and other organ involvement. Interleukin (IL)-27 with its pro- and anti-inflammatory effects might be an important effective cytokine in this disease. The aim of this study was to investigate the association of IL-27 serum concentration and a single-nucleotide polymorphism (SNP) rs153109 (-964 A > G) with the risk and clinical features of the patients with BD. IL-27 Genotyping was performed using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) and the IL-27 serum levels were measured using enzyme-linked immunosorbent assay (ELISA). It is shown that AG, GG, and AG + GG genotypes, as well as G allele of rs153109, can significantly increase the risk of BD in total and in male individuals. Significantly higher frequencies of AG and GG genotypes and G allele were observed in total and male patients with an active form of BD. AG and GG genotypes were associated with joint (p = 0.046) and vascular (p = 0.02) involvement. The frequency of the G allele was higher in all patients, as well as in female patients with vascular involvement (p = 0.02). Serum cytokine analysis indicated an increased level of IL-27 in BD patients compared to healthy subjects (p = 0.038). Additionally, a higher level of IL-27 was detected in patients carrying the rs153109 GG genotype (p = 0.04) and those with renal (p = 0.009) and skin (p = 0.05) involvement. In conclusion, this study underscores the involvement of IL-27 rs153109 variants and increased serum level in BD susceptibility and pathogenesis.

在伊朗人群中,白细胞介素27基因变异rs153109与细胞因子血清水平升高和behet病易感性相关。
白塞病(BD)是一种全身性血管炎,以复发性口腔溃疡、生殖器溃疡、眼部病变和其他器官受累为特征。白细胞介素(IL)-27具有促炎和抗炎作用,可能是本病重要的有效细胞因子。采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)和酶联免疫吸附试验(ELISA)检测血清IL-27水平,探讨血清IL-27浓度和单核苷酸多态性(SNP) rs153109 (-964 a > G)与BD患者发病风险和临床特征的关系。结果表明,AG、GG和AG + GG基因型以及rs153109的G等位基因可显著增加总体和男性个体患BD的风险。AG和GG基因型及G等位基因的频率在男性和男性BD活动性患者中均明显较高。AG和GG基因型与关节(p = 0.046)和血管(p = 0.02)受损伤相关。G等位基因的频率在所有患者中都较高,在血管受累的女性患者中也是如此(p = 0.02)。血清细胞因子分析显示,与健康受试者相比,BD患者IL-27水平升高(p = 0.038)。此外,携带rs153109 GG基因型的患者(p = 0.04)以及肾脏(p = 0.009)和皮肤(p = 0.05)受损伤的患者中检测到较高水平的IL-27。总之,本研究强调IL-27 rs153109变异和血清水平升高参与双相障碍的易感性和发病机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
European cytokine network
European cytokine network 生物-免疫学
CiteScore
5.70
自引率
0.00%
发文量
5
审稿时长
6 months
期刊介绍: The journal that brings together all areas of work involving cytokines. European Cytokine Network is an electronic journal that publishes original articles and abstracts every quarter to provide an essential bridge between researchers and clinicians with an interest in this cutting-edge field. The journal has become a must-read for specialists in the field thanks to its swift publication and international circulation. The journal is referenced in several databases, including Medline, which is testament to its scientific quality.
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