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RNASET2标签单核苷酸多态性而非CCR6基因多态性与中国汉族人群自身免疫性甲状腺疾病相关。

RNASET2 tag SNP but not CCR6 polymorphisms is associated with autoimmune thyroid diseases in the Chinese Han population.

作者信息

Chen Xiao-jun, Gong Xiao-hua, Yan Ni, Meng Shuai, Qin Qiu, Jiang Yan-Fei, Zheng Hai-Yan, Zhang Jin-an

机构信息

Department of Endocrinology, The First Affiliated Hospital of Wenzhou Medical University, No.2 Fuxuexiang Road, Ouhai District, 325000, Wenzhou, China.

Department of Endocrinology, Jinshan Hospital of Fudan University, No.1508 Longhang Road, Jinshan District, 201508, Shanghai, China.

出版信息

BMC Med Genet. 2015 Feb 26;16:11. doi: 10.1186/s12881-015-0150-9.

Abstract

BACKGROUND

Polymorphisms of the CC chemokine receptor 6 (CCR6) and RNASET2 tag SNP have been shown to be associated with the susceptibility to several immune-related diseases. This study was conducted to identify the association of CCR6 and RNASET2 tag SNP with autoimmune thyroid diseases (AITDs) in the Chinese Han population.

METHODS

We enrolled 1061 patients with AITDs, including 701 patients with Graves' disease (GD) and 360 patients with Hashimoto's thyroiditis (HT), and 938 healthy individuals for a case-control genetic association study. Three CCR6 single nucleotides polymorphisms (SNPs) (rs3093023/rs3093024/rs6902119) and one tagging SNP (rs9355610) within RNASET2 gene were selected for genotyping by multiplex polymerase chain reaction (PCR) and ligase detection reaction (LDR).

RESULTS

The frequency of rs9355610 genotypes in the patients with GD differed significantly from that in the controls (p = 0.017). The frequency of the minor G allele of rs9355610 was significantly higher in the GD patients than in the healthy controls (p = 0.005, OR = 1.225, 95% CI:1.063-1.412). However, we could not find significant differences in the genotype or allele frequencies of HT patients compared with healthy controls. After gender stratification, the frequency of the minor G allele in both male and female GD patients was significantly higher than that in the healthy controls (p = 0.036, OR = 1.308, 95% CI:1.017-1.684 ; p = 0.048, OR = 1.19, 95% CI:1.001-1.413; respectively);. Furthermore, the frequency of haplotype AT in GD patients was significantly lower than that in their control groups (p = 0.003) and showed a protective effect against GD (OR = 0.806, 95% CI: 0.699-0.929). The frequency of haplotype GT in GD patients was significantly higher than that in their control groups (p = 0.048), indicating that GT was the risk haplotype to GD (OR = 1.267, 95% CI: 1.001-1.603). There were no significant differences in the allele or genotype frequencies of three SNPs of CCR6 (rs3093023/rs3093024/ rs6902119) gene between GD patients, HT patients and controls.

CONCLUSIONS

Our results suggest that the rs9355610 tag SNP of RNASET2 gene is positively associated with susceptibility to GD in the Chinese Han population. No association was found for the tested CCR6 SNPs.

摘要

背景

CC趋化因子受体6(CCR6)和RNASET2标签单核苷酸多态性(SNP)已被证明与多种免疫相关疾病的易感性有关。本研究旨在确定中国汉族人群中CCR6和RNASET2标签SNP与自身免疫性甲状腺疾病(AITD)的相关性。

方法

我们纳入了1061例AITD患者,包括701例格雷夫斯病(GD)患者和360例桥本甲状腺炎(HT)患者,以及938名健康个体进行病例对照基因关联研究。通过多重聚合酶链反应(PCR)和连接酶检测反应(LDR)对RNASET2基因内的三个CCR6单核苷酸多态性(SNP)(rs3093023/rs3093024/rs6902119)和一个标签SNP(rs9355610)进行基因分型。

结果

GD患者中rs9355610基因型的频率与对照组有显著差异(p = 0.017)。rs9355610的次要G等位基因在GD患者中的频率显著高于健康对照组(p = 0.005,OR = 1.225,95%CI:1.063 - 1.412)。然而,与健康对照组相比,我们未发现HT患者的基因型或等位基因频率有显著差异。按性别分层后,男性和女性GD患者中次要G等位基因的频率均显著高于健康对照组(分别为p = 0.036,OR = 1.308,95%CI:1.017 - 1.684;p = 0.048,OR = 1.19,95%CI:1.001 - 1.413)。此外,GD患者中单体型AT的频率显著低于其对照组(p = 0.003),并对GD显示出保护作用(OR = 0.806,95%CI:0.699 - 0.929)。GD患者中单体型GT的频率显著高于其对照组(p = 0.048),表明GT是GD的风险单体型(OR = 1.267,95%CI:1.001 - 1.603)。CCR6(rs3093023/rs3093024/rs6902119)基因的三个SNP的等位基因或基因型频率在GD患者、HT患者和对照组之间无显著差异。

结论

我们的结果表明,RNASET2基因的rs9355610标签SNP与中国汉族人群中GD的易感性呈正相关。未发现所检测CCR6 SNP的关联。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cb8/4422281/398aaff8f30a/12881_2015_150_Fig1_HTML.jpg

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