Yan Ni, Meng Shuai, Zhou Jiaozhen, Xu Jian, Muhali Fatuma Said, Jiang Wenjuan, Shi Liangfeng, Shi Xiaohong, Zhang Jinan
Department of Endocrinology, Jinshan Hospital of Fudan University, No. 1508 Longhang Road, Jinshan District, Shanghai 201508, China.
Int J Mol Sci. 2014 Jul 11;15(7):12280-93. doi: 10.3390/ijms150712280.
The STAT4 gene encodes a transcriptional factor that transmits signals induced by several key cytokines which play important roles in the development of autoimmune diseases. The aim of this study was to explore the association of STAT4 polymorphism with Graves' disease (GD) and Hashimoto's thyroiditis (HT). A total of 1048 autoimmune thyroid diseases (AITDs) patients (693 with GD and 355 with HT) and 909 age- and gender-matched controls were examined. STAT4 polymorphisms (rs7574865/rs10181656/ rs7572482) were genotyped by multiplex polymerase chain reaction (PCR) and ligase detection reaction (LDR). The results indicated that the frequencies of rs7574865 genotypes in patients with GD differed significantly from the controls (p=0.028), the T allele frequency of GD patients was also significantly higher than the controls (p=0.020). The genotypes of rs10181656 differed significantly in GD patients from controls (p=0.012); G allele frequencies were significantly higher in AITD patients than the controls (p=0.014 and 0.031, respectively). The frequencies of haplotype GC with GD and HT patients were significantly lower than their controls (p=0.015 and 0.030, respectively). In contrast, the frequencies of haplotype TG with GD and HT patients were significantly higher than their controls (p=0.016 and 0.048, respectively). These findings strongly suggest that STAT4 rs7574865/rs10181656 polymorphisms increase the risk of AITD in a Chinese population.
信号转导和转录激活因子4(STAT4)基因编码一种转录因子,该转录因子可传递由几种关键细胞因子诱导产生的信号,这些细胞因子在自身免疫性疾病的发展中起重要作用。本研究旨在探讨STAT4基因多态性与格雷夫斯病(GD)和桥本甲状腺炎(HT)的相关性。共检测了1048例自身免疫性甲状腺疾病(AITD)患者(693例GD患者和355例HT患者)以及909例年龄和性别匹配的对照。通过多重聚合酶链反应(PCR)和连接酶检测反应(LDR)对STAT4基因多态性(rs7574865/rs10181656/rs7572482)进行基因分型。结果表明,GD患者中rs7574865基因型的频率与对照组有显著差异(p = 0.028),GD患者的T等位基因频率也显著高于对照组(p = 0.020)。rs10181656的基因型在GD患者和对照组之间有显著差异(p = 0.012);AITD患者的G等位基因频率显著高于对照组(分别为p = 0.014和0.031)。GD和HT患者的单倍型GC频率显著低于对照组(分别为p = 0.015和0.030)。相反,GD和HT患者的单倍型TG频率显著高于对照组(分别为p = 0.016和0.048)。这些发现强烈表明,STAT4 rs7574865/rs10181656多态性增加了中国人群患AITD的风险。