Suppr超能文献

自身免疫性甲状腺疾病中1型和2型碘甲状腺原氨酸脱碘酶基因的功能多态性

Functional Polymorphisms of the Type 1 and Type 2 Iodothyronine Deiodinase Genes in Autoimmune Thyroid Diseases.

作者信息

Inoue Naoya, Watanabe Mikio, Katsumata Yuka, Ishido Naoko, Hidaka Yoh, Iwatani Yoshinori

机构信息

a Department of Biomedical Informatics, Division of Health Sciences , Osaka University Graduate School of Medicine , Osaka , Japan.

b Laboratory for Clinical Investigation , Osaka University Hospital , Osaka , Japan.

出版信息

Immunol Invest. 2018 Jul;47(5):534-542. doi: 10.1080/08820139.2018.1458861. Epub 2018 Apr 12.

Abstract

Graves' disease (GD) and Hashimoto's disease (HD) are major autoimmune thyroid diseases (AITDs), and their pathological conditions vary among patients. Type 1 iodothyronine deiodinase (D1) and type 2 iodothyronine deiodinase (D2) convert from thyroxine (T4) to triiodothyronine (T3). However, few findings have been described concerning the association between polymorphisms in D1 and D2 genes and AITD. Therefore, we genotyped D1 rs11206244, D2 rs225014, and rs12885300 polymorphisms in 134 GD patients, including 54 patients with intractable GD and 44 patients with GD in remission and 132 HD patients, including 57 patients with severe HD, 45 patients with mild HD, and 84 healthy controls using PCR-RFLP. In the D2 rs225014 polymorphism, the TT genotype, which was correlated with higher D2 activity, was less frequent in AITD, especially in HD, than in control subjects (P = 0.0032 and 0.0002, respectively). Moreover, they were also less frequent in HD than in GD (P = 0.0199). The TT genotype and T allele were less frequent in severe HD and mild HD than in control subjects (P = 0.0003, 0.0006, 0.0432, and 0.0427, respectively). In conclusion, the low frequency of the TT genotype D2 rs225014 polymorphism was associated with the development of AITD and severity of HD.

摘要

格雷夫斯病(GD)和桥本氏病(HD)是主要的自身免疫性甲状腺疾病(AITD),其病理状况因患者而异。1型碘甲状腺原氨酸脱碘酶(D1)和2型碘甲状腺原氨酸脱碘酶(D2)可将甲状腺素(T4)转化为三碘甲状腺原氨酸(T3)。然而,关于D1和D2基因多态性与AITD之间的关联,鲜有研究报道。因此,我们采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)技术,对134例GD患者(包括54例难治性GD患者和44例缓解期GD患者)以及132例HD患者(包括57例重度HD患者、45例轻度HD患者)和84例健康对照者的D1 rs11206244、D2 rs225014和rs12885300多态性进行了基因分型。在D2 rs225014多态性中,与较高D2活性相关的TT基因型在AITD患者中,尤其是在HD患者中,出现频率低于对照组(分别为P = 0.0032和0.0002)。此外,HD患者中该基因型出现频率也低于GD患者(P = 0.0199)。重度HD和轻度HD患者中TT基因型和T等位基因出现频率低于对照组(分别为P = 0.0003、0.0006、0.0432和0.0427)。总之,D2 rs225014多态性的TT基因型出现频率较低与AITD的发生及HD的严重程度相关。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验