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阿根廷人群中甲状腺球蛋白基因 TGrI29 微卫星与自身免疫性甲状腺炎的关联:病例对照研究。

Association of the TGrI29 microsatellite in thyroglobulin gene with autoimmune thyroiditis in a Argentinian population: a case-control study.

机构信息

Laboratorio de Biología Molecular, Cátedra de Genética y Biología Molecular, Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires, Junín 956, 1113 Buenos Aires, Argentina.

出版信息

Endocrine. 2010 Dec;38(3):320-7. doi: 10.1007/s12020-010-9398-1. Epub 2010 Oct 23.

Abstract

Autoimmune thyroid disease (AITD) is a multifactorial disorder that involves a putative association with thyroid autoantigen-specific and immune regulatory genes, as well as environmental factors. The thyroglobulin gene is the main identified thyroid autoantigen-specific gene associated to autoimmune thyroiditis. The aim of this work was to test for evidence of allelic association between autoimmune thyroiditis (AT) and thyroglobulin polymorphism markers in Argentinian patients. We studied six polymorphisms distributed throughout all the thyroglobulin gene: four microsatellites (Tgms1, Tgms2, TGrI29, and TGrI30), one insertion/deletion polymorphism (IndelTG-IVS18), and one exonic single nucleotide polymorphism (c.7589G>A) in 100 AT patients and 100 healthy control subjects. No differences in allele and genotype frequencies distribution were observed between autoimmune thyroiditis cases and controls for Tgms1, Tgms2, TGrI30, IndelTG-IVS18, and c.7589G>A. However, when we analyzed autoimmune thyroiditis patients with the TGrI29 microsatellite we found a significant association between the 197-bp allele and autoimmune thyroiditis (33.50% vs. 19.00% in control group) (P = 0.001). In addition, a significant major prevalence of the 197/201-bp genotype has been also seen in autoimmune thyroiditis subjects (59% vs. 24% in control group, P < 0.0001). In conclusion, our work showed the association between the thyroglobulin gene and autoimmune thyroiditis in Argentinian population and supports the described evidence of thyroglobulin as a thyroid-specific gene linked to AITD.

摘要

自身免疫性甲状腺疾病(AITD)是一种多因素疾病,涉及甲状腺自身抗原特异性和免疫调节基因以及环境因素的假定关联。甲状腺球蛋白基因是与自身免疫性甲状腺炎相关的主要鉴定的甲状腺自身抗原特异性基因。本工作旨在检测阿根廷患者自身免疫性甲状腺炎(AT)与甲状腺球蛋白多态性标记物之间的等位基因关联证据。我们研究了分布在整个甲状腺球蛋白基因中的六个多态性:四个微卫星(Tgms1、Tgms2、TGrI29 和 TGrI30)、一个插入/缺失多态性(IndelTG-IVS18)和一个外显子单核苷酸多态性(c.7589G>A)在 100 例 AT 患者和 100 例健康对照组中。在自身免疫性甲状腺炎病例和对照组中,Tgms1、Tgms2、TGrI30、IndelTG-IVS18 和 c.7589G>A 的等位基因和基因型频率分布无差异。然而,当我们分析甲状腺球蛋白基因的 TGrI29 微卫星时,我们发现 197-bp 等位基因与自身免疫性甲状腺炎之间存在显著关联(33.50% vs. 对照组中的 19.00%)(P=0.001)。此外,自身免疫性甲状腺炎患者中 197/201-bp 基因型的主要流行率也显著升高(59% vs. 对照组中的 24%,P<0.0001)。总之,我们的工作显示了甲状腺球蛋白基因与阿根廷人群自身免疫性甲状腺炎之间的关联,并支持了甲状腺球蛋白作为与 AITD 相关的甲状腺特异性基因的描述性证据。

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