TSHR基因(rs179247)多态性与自身免疫性甲状腺疾病的易感性:系统回顾与元分析》。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-08-01 DOI:10.3803/EnM.2024.1987
Hendra Zufry, Timotius Ivan Hariyanto
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引用次数: 0

摘要

背景:巴塞杜氏病(GD)和桥本氏甲状腺炎(HT)都被归类为自身免疫性甲状腺疾病(AITD)。据推测,促甲状腺激素受体(TSHR)基因的变化可能会导致这些疾病的发生。本研究旨在分析 TSHR rs179247 基因多态性与 AITD 易感性之间的相关性:我们利用相关关键词对谷歌学术、Scopus、Medline 和 Cochrane 图书馆数据库进行了全面检索,检索期截至 2024 年 3 月 2 日。本综述研究了 TSHR rs179247 与 AITD 易感性之间的相关数据。采用随机效应模型评估了几率比(OR),结果与各自的 95% 置信区间(CIs)一起呈现:荟萃分析包括 12 项研究。TSHR rs179247 基因多态性的所有遗传模型都与广东话发病风险增加有关。特别是在显性模型中观察到了相关性(OR,1.65;PC结论:本研究表明,TSHR rs179247 基因多态性与 GD 患病风险增加有关,但与高血压无关,因此可作为一种潜在的生物标志物。
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TSHR Gene (rs179247) Polymorphism and Susceptibility to Autoimmune Thyroid Disease: A Systematic Review and Meta-Analysis.

Backgruound: Both Graves' disease (GD) and Hashimoto's thyroiditis (HT) are classified as autoimmune thyroid diseases (AITDs). It has been hypothesized that changes in the thyroid-stimulating hormone receptor (TSHR) gene may contribute to the development of these conditions. This study aimed to analyze the correlation between the TSHR rs179247 gene polymorphism and susceptibility to AITD.

Methods: We conducted a thorough search of the Google Scholar, Scopus, Medline, and Cochrane Library databases up until March 2, 2024, utilizing a combination of relevant keywords. This review examines data on the association between TSHR rs179247 and susceptibility to AITD. Random-effect models were employed to assess the odds ratio (OR), and the findings are presented along with their respective 95% confidence intervals (CIs).

Results: The meta-analysis included 12 studies. All genetic models of the TSHR rs179247 gene polymorphism were associated with an increased risk of developing GD. Specifically, the associations were observed in the dominant model (OR, 1.65; P<0.00001), recessive model (OR, 1.65; P<0.00001), as well as for the AA genotype (OR, 2.09; P<0.00001), AG genotype (OR, 1.39; P<0.00001), and A allele (OR, 1.44; P<0.00001). Further regression analysis revealed that these associations were consistent regardless of the country of origin, sample size, age, and sex distribution. However, no association was found between TSHR rs179247 and the risk of HT across all genetic models.

Conclusion: This study suggests that the TSHR rs179247 gene polymorphism is associated with an increased risk of GD, but not with HT, and may therefore serve as a potential biomarker.

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CiteScore
7.20
自引率
4.30%
发文量
567
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