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信号转导和转录激活因子4单核苷酸多态性与伊朗青少年类风湿关节炎患者之间无关联。

Lack of Association between STAT4 Single Nucleotide Polymorphisms and Iranian Juvenile Rheumatoid Arthritis Patients.

作者信息

Aslani Saeed, Mahmoudi Mahdi, Salmaninejad Arash, Poursani Shiva, Ziaee Vahid, Rezaei Nima

机构信息

a Rheumatology Research Center , Tehran University of Medical Sciences , Tehran , Iran.

b Department of Immunology, School of Medicine , Tehran University of Medical Sciences , Tehran , Iran.

出版信息

Fetal Pediatr Pathol. 2017 Jun;36(3):177-183. doi: 10.1080/15513815.2016.1253809. Epub 2017 Mar 2.

DOI:10.1080/15513815.2016.1253809
PMID:28524764
Abstract

Juvenile rheumatoid arthritis (JRA) is a common chronic systemic autoimmune disease in children. Single nucleotide polymorphisms (SNPs) of signal transducer and activator of transcription 4 (STAT4) gene are suspected to have association with the risk of autoimmune diseases. Previous investigations have indicated that the STAT4 rs7574865 T allele was significantly associated with rheumatoid arthritis. In this study, we aimed to evaluate the association of STAT4 SNPs with JRA in Iranian population. T allele of STAT4 rs7574865 SNP was less frequent in patients than in controls, and the difference was not significant (p = 0.19, OR = 0.72, 95% CI: 0.44 -1.17). In addition, G allele of this SNP was frequent but not significant in JRA patients (p = 0.19, OR = 1.38, 95% CI: 0.85-2.25). Neither alleles nor genotypes of rs7601754 SNP of STAT4 gene demonstrated associations with JRA. We recognize that gene variants of STAT4 did not affect JRA susceptibility in Iranian population.

摘要

青少年类风湿性关节炎(JRA)是儿童常见的慢性全身性自身免疫性疾病。信号转导和转录激活因子4(STAT4)基因的单核苷酸多态性(SNP)被怀疑与自身免疫性疾病的风险有关。先前的研究表明,STAT4 rs7574865 T等位基因与类风湿性关节炎显著相关。在本研究中,我们旨在评估伊朗人群中STAT4 SNP与JRA的关联。STAT4 rs7574865 SNP的T等位基因在患者中的频率低于对照组,差异无统计学意义(p = 0.19,OR = 0.72,95% CI:0.44 - 1.17)。此外,该SNP的G等位基因在JRA患者中频率较高,但差异无统计学意义(p = 0.19,OR = 1.38,95% CI:0.85 - 2.25)。STAT4基因rs7601754 SNP的等位基因和基因型均未显示与JRA有关联。我们认识到,在伊朗人群中,STAT4的基因变异不会影响JRA易感性。

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