Atabaki Mahdi, Hashemi Mohammad, Daneshvar Hamid, Alijani Ebrahim
Clinical Immunology Research Center, Zahedan University of Medical Sciences, Zahedan, Sistan and Baluchestan 98167-43181, Iran.
Cellular and Molecular Research Center, Zahedan University of Medical Sciences, Zahedan, Sistan and Baluchestan 98167-43181, Iran.
Biomed Rep. 2017 Mar;6(3):335-338. doi: 10.3892/br.2017.855. Epub 2017 Feb 9.
Rheumatoid arthritis (RA) is a systemic autoimmune disease predominantly involving the synovial joints and affects up to 1% of adults worldwide. The aim of the present study was to determine whether the interleukin-1 receptor (IL1R)-associated kinase () rs3027898 gene polymorphism confers susceptibility to RA in a sample of patients from Iran. This gene encodes IRAK1, one of two putative serine/threonine kinases that associates with IL1R upon stimulation. is partially responsible for IL-1-induced upregulation of the transcription factor, nuclear factor-κB. The present case-control study was performed on 120 patients with RA and 120 healthy individuals. Genomic DNA was extracted from whole blood, and the gene polymorphism was evaluated using a tetra-primer amplification refractory mutation system-polymerase chain reaction method. The results demonstrated that there was no association between IRAK1 rs3027898 CA genotype and the risk of RA in women (odds ratio=0.72, 95% confidence interval=0.41-1.49; P=0.446). Further studies with larger sample sizes and different ethnicities are required to validate the present findings.
类风湿关节炎(RA)是一种主要累及滑膜关节的全身性自身免疫性疾病,全球成年人群中患病率高达1%。本研究旨在确定白细胞介素-1受体(IL1R)相关激酶()rs3027898基因多态性是否会使来自伊朗的患者样本易患RA。该基因编码IRAK1,它是两种假定的丝氨酸/苏氨酸激酶之一,在受到刺激时与IL1R结合。 部分负责IL-1诱导的转录因子核因子-κB的上调。本病例对照研究针对120例RA患者和120名健康个体进行。从全血中提取基因组DNA,并使用四引物扩增阻滞突变系统-聚合酶链反应方法评估基因多态性。结果表明,IRAK1 rs3027898 CA基因型与女性RA风险之间无关联(优势比=0.72,95%置信区间=0.41-1.49;P=0.446)。需要更大样本量和不同种族的进一步研究来验证本研究结果。