Hadinedoushan Hossein, Noorbakhsh Parisa, Soleymani-Salehabadi Hossein
Department of Immunology, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.
Department of Rheumatology, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.
Arch Rheumatol. 2016 Jul 27;31(4):306-313. doi: 10.5606/ArchRheumatol.2016.5907. eCollection 2016 Dec.
This study aims to determine whether promoter -238 G/A polymorphism in tumor necrosis factor-alpha (TNF-α) gene is associated with susceptibility to rheumatoid arthritis (RA) in Iranian population and serum level of TNF-a.
This case-controlled study was performed on two groups including 90 RA patients (20 males, 70 females; mean age 50.3 years; range 26 to 65 years) and 90 healthy controls (21 males, 69 females; mean age 48.6 years; range 27 to 63 years). We determined the frequency of -238 G/A TNF-a gene polymorphism by polymerase chain reaction restriction fragment length polymorphism. We measured the serum level of TNF-a using enzyme-linked immunosorbent assay method. Also, we determined the association of serum TNF-a level with the polymorphism in RA patients.
There was no significant difference in terms of sex and age in the two groups. In the RA group, the genotype frequency of -238 G/A polymorphism was GG (76.6%), GA (17.8%), and AA (5.6%). In the control group, the genotype frequency of -238 G/A polymorphism was GG (83.5%), GA (8.8%), and AA (7.7%). Statistical analysis showed no significant difference in the genotype frequency of this polymorphism between two groups (p=0.07). The serum level of TNF-a were 5.21±1.69 Pg/mL (range 0 to 11.6) in the control group and 62.4±27.1 Pg/mL (range 0 to 117.22) in the RA group (p<0.0001). There was no significant difference in terms of serum TNF-a level and different genotypes in the RA group (p=0.5).
Our findings demonstrate that the TNF-a -238 G/A gene polymorphism may not represent a significant risk factor for RA in Iranian population and there is no association between the polymorphism and serum TNF-a level in RA patients.
本研究旨在确定肿瘤坏死因子-α(TNF-α)基因启动子-238 G/A多态性是否与伊朗人群类风湿关节炎(RA)易感性及血清TNF-α水平相关。
本病例对照研究纳入两组,包括90例RA患者(20例男性,70例女性;平均年龄50.3岁;范围26至65岁)和90例健康对照者(21例男性,69例女性;平均年龄48.6岁;范围27至63岁)。我们采用聚合酶链反应-限制性片段长度多态性方法确定-238 G/A TNF-α基因多态性的频率。使用酶联免疫吸附测定法测量血清TNF-α水平。此外,我们还确定了RA患者血清TNF-α水平与多态性之间的关联。
两组在性别和年龄方面无显著差异。在RA组中,-238 G/A多态性的基因型频率为GG(76.6%)、GA(17.8%)和AA(5.6%)。在对照组中,-238 G/A多态性的基因型频率为GG(83.5%)、GA(8.8%)和AA(7.7%)。统计分析显示两组间该多态性的基因型频率无显著差异(p = 0.07)。对照组血清TNF-α水平为5.21±1.69 Pg/mL(范围0至11.6),RA组为62.4±27.1 Pg/mL(范围0至117.22)(p < 0.0001)。RA组血清TNF-α水平与不同基因型之间无显著差异(p = 0.5)。
我们的研究结果表明,TNF-α -238 G/A基因多态性可能不是伊朗人群RA的重要危险因素,且该多态性与RA患者血清TNF-α水平无关。