自身免疫性甲状腺疾病中TRAF3IP2和SIGIRR基因多态性及其表达水平的实现

Q2 Health Professions
Mona A Abbas, Raouth E Girgis, Hytham R Badr, Ahmed E Abdel Meguid, Eman A E Badr
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引用次数: 0

摘要

遗传在自身免疫性甲状腺疾病(AITDs)的发展中起着至关重要的作用,包括Graves病(GD)和桥本甲状腺炎(HT)。本研究评估了TRAF3IP2和SIGIRR基因表达及其多态性(分别为rs13210247和rs7396562)与AITDs风险的关系。150名参与者(50名GD, 50名HT和50名对照组)的基因表达和多态性基因分型通过实时PCR进行评估。TRAF3IP2在GD和HT中的表达明显高于对照组。回归分析显示TRAF3IP2 rs13210247与GD和HT风险显著相关。AG基因型证明与GD风险有相当大的关系。同时,AG基因型和G等位基因与HT发病率有显著关系。与对照组相比,GD和HT组SIGIRR表达明显下调。对于rs7396562,回归分析显示CA、AA、CA+AA基因型和A等位基因与GD风险显著相关。它们还与高血压风险显著相关。我们认为TRAF3IP2和SIGIRR基因表达的改变及其遗传变异可能与AITDs易感性有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Implementation of TRAF3IP2 and SIGIRR gene polymorphisms and their expression levels in autoimmune thyroid diseases.

Genetics plays a crucial role in the development of autoimmune thyroid diseases (AITDs), including Graves' disease (GD) and Hashimoto's thyroiditis (HT). This study evaluated the relationship between TRAF3IP2 and SIGIRR gene expression, their polymorphisms (rs13210247 and rs7396562, respectively), and AITDs risk. Gene expression and polymorphism genotyping were assessed by real-time PCR in 150 participants (50 GD, 50 HT, and 50 controls). TRAF3IP2 expression was considerably higher in GD and HT in contrast to controls. Regression analysis of TRAF3IP2 rs13210247 demonstrated a significant association with GD and HT risk. The AG genotype proved a considerable relationship with GD risk. At the same time, the AG genotype and the G allele exhibited a notable relationship with HT incidence. SIGIRR expression was notably downregulated in GD and HT versus controls. For rs7396562, the regression analysis demonstrated that the CA, AA, CA+AA genotypes, and A allele significantly correlated with GD risk. They are also notably linked with HT risk. We concluded that altered TRAF3IP2 and SIGIRR gene expression and their genetic variants may contribute to AITDs susceptibility.

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来源期刊
CiteScore
3.50
自引率
0.00%
发文量
38
审稿时长
>12 weeks
期刊介绍: The Journal of Immunoassay & Immunochemistry is an international forum for rapid dissemination of research results and methodologies dealing with all aspects of immunoassay and immunochemistry, as well as selected aspects of immunology. They include receptor assay, enzyme-linked immunosorbent assay (ELISA) in all of its embodiments, ligand-based assays, biological markers of ligand-receptor interaction, in vivo and in vitro diagnostic reagents and techniques, diagnosis of AIDS, point-of-care testing, clinical immunology, antibody isolation and purification, and others.
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