Department of Endocrinology, Shanghai University of Medicine & Health Sciences Affiliated Zhoupu Hospital, No. 1500 Zhouyuan Road, Pudong District, Shanghai, China 201318.
Department of Endocrinology, Jinshan Hospital of Fudan University, No. 1508 Longhang Road, Jinshan District, Shanghai, China 201508.
J Immunol Res. 2022 Apr 26;2022:3881417. doi: 10.1155/2022/3881417. eCollection 2022.
To explore the association of gene polymorphisms with autoimmune thyroid diseases (AITDs) including Hashimoto's thyroiditis (HT) and Graves' illness (GD) as well as their clinical features.
rs6568431, rs548234, and rs6937876 were selected to investigate the correlation of single-nucleotide polymorphisms of gene with AITDs. Their frequencies in 824 AITD patients, including 271 HT patients and 553 GD patients, and 764 healthy controls were tested using both ligase detection reaction and multiplex polymerase chain reaction.
Allele A frequency of rs6568431 in AITDs patients ( = 0.016, OR = 1.201, 95% CI = 1.034 - 1.394) and allele G frequency of rs6937876 in AITDs patients ( = 0.009, OR = 1.223, 95% CI = 1.052 - 1.422) and in GD patients ( = 0.009, OR = 1.247, 95% CI = 1.056 - 1.473) were significantly higher than those in the healthy controls. The frequency of G allele ( = 5.42E - 18, OR = 0.242, 95% CI = 0.173 - 0.339) of rs6937876 was significantly higher in GD patients with ophthalmopathy. However, no relationship was found between family history, age onset, and the three SNPs.
The study is the first to reveal the association between AITDs and polymorphisms, and gene is considered as a predisposing gene to AITDs, especially GDs.
探讨基因多态性与包括桥本甲状腺炎(HT)和格雷夫斯病(GD)在内的自身免疫性甲状腺疾病(AITD)以及它们的临床特征之间的关联。
选择 rs6568431、rs548234 和 rs6937876 来研究基因单核苷酸多态性与 AITD 的相关性。通过连接酶检测反应和多重聚合酶链反应,检测 824 例 AITD 患者(包括 271 例 HT 患者和 553 例 GD 患者)和 764 例健康对照者中这些单核苷酸多态性的频率。
AITD 患者 rs6568431 的等位基因 A 频率( = 0.016,OR = 1.201,95% CI = 1.034 - 1.394)和 AITD 患者( = 0.009,OR = 1.223,95% CI = 1.052 - 1.422)和 GD 患者 rs6937876 的等位基因 G 频率( = 0.009,OR = 1.247,95% CI = 1.056 - 1.473)明显高于健康对照组。GD 伴眼病患者 rs6937876 的 G 等位基因频率( = 5.42E-18,OR = 0.242,95% CI = 0.173 - 0.339)明显升高。然而,未发现家族史、发病年龄与这三个 SNP 之间存在相关性。
本研究首次揭示了 AITD 与基因多态性之间的关联,并且基因被认为是 AITD,特别是 GD 的易感基因。