Li Miao, Liu Bailing, Li Lu, Zhang Chen, Zhou Qi
Department of Ultrasound, Second Affiliated Hospital, School of Medicine, Xi'an Jiaotong University, Xi'an, China.
Department of Ultrasound, Children's Hospital of Xi'an, Xi'an, China.
J Hum Genet. 2015 Aug;60(8):427-33. doi: 10.1038/jhg.2015.42. Epub 2015 May 28.
Although the connection between SEPS1 gene variants and Hashimoto's thyroiditis (HT) has been established in Europeans, the relationship between the SEPS1 gene and HT remains unclear in Han Chinese. Here we aimed to investigate the potential association between SEPS1 variants and HT in the Han population. In addition, the effects of SEPS1 haplotypes on the susceptibility of the development of immune-mediated diseases with an inflammatory component will also be evaluated. Seven single-nucleotide polymorphisms (SNPs) with minor allele frequency ⩾0.05 were genotyped in 1013 HT patients and 2998 healthy controls from genetically independent Han Chinese individuals. We identified that the rs28665122 SNP was significantly associated with HT, both in the female group (allelic P=0.002644 and genotypic P=0.010326) and the combined data set (allelic P=0.000518 and genotypic P=0.002731). Further analyses based on haplotypes indicated that a two-SNP haplotype (rs2009895-rs28665122) was significantly associated with HT (global P=0.0036), which was also observed in females (global P=0.0162) but not in males. Our findings provide further supporting evidence that confirms the results of previous studies, which suggested potential roles of the SEPS1 gene in the pathogenesis and etiology of HT.
尽管在欧洲人群中已证实SEPS1基因变异与桥本甲状腺炎(HT)之间存在关联,但在汉族人群中,SEPS1基因与HT的关系仍不清楚。在此,我们旨在研究汉族人群中SEPS1变异与HT之间的潜在关联。此外,还将评估SEPS1单倍型对具有炎症成分的免疫介导疾病易感性的影响。在来自基因独立的汉族个体的1013例HT患者和2998例健康对照中,对7个次要等位基因频率⩾0.05的单核苷酸多态性(SNP)进行了基因分型。我们发现,rs28665122 SNP与HT显著相关,在女性组(等位基因P = 0.002644,基因型P = 0.010326)和合并数据集(等位基因P = 0.000518,基因型P = 0.002731)中均如此。基于单倍型的进一步分析表明,一个双SNP单倍型(rs2009895-rs28665122)与HT显著相关(全局P = 0.003),在女性中也观察到这种相关性(全局P = 0.0162),但在男性中未观察到。我们的研究结果提供了进一步的支持证据,证实了先前研究的结果,表明SEPS1基因在HT的发病机制和病因学中具有潜在作用。