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CTLA-4 +49 基因多态性与 Graves 病易感性的荟萃分析。

Meta-Analysis of CTLA-4 +49 Gene Polymorphism and Susceptibility to Graves' Disease.

机构信息

Department of Endocrinology, Hematology and Nephrology of Zhongwei People's Hospital of Ningxia, Zhongwei, Ningxia, China.

Key Laboratory of Fertility Preservation and Maintenance (NXMU), Ministry of Education, Ningxia Medical University, Yinchuan, Ningxia, China.

出版信息

Crit Rev Eukaryot Gene Expr. 2020;30(5):377-390. doi: 10.1615/CritRevEukaryotGeneExpr.2020034872.

Abstract

UNLABELLED

Cytotoxic T lymphocyte-associated antigen-4 (CTLA-4) plays an important role in the initiation and development of Graves' disease (GD), especially CTLA-4 +49A/G polymorphism and genetic susceptibility to GD. However, the current conclusions are consistent. Therefore, this study adopted meta-analysis method to assess the exact correlation between this polymorphism and GD risk.

METHODS

Literature searches were performed in PubMed, Embase, Web of Science, China National Knowledge Infrastructure, China Wanfang, and other databases for data on the correlation between polymorphisms of CTLA-4 +49A/G and GD risk. The end date for publications was May 2020. Stata 15.0 software was used for data analysis.

RESULTS

A total of 33 papers were included, covering 8,555 cases and 9,533 controls. The results showed that the CTLA-4 +49 allele G compared to allele A, odds ratio (OR) = 1.62, 95% CI [1.56, 2.09]. In the dominant, recessive, homozygous, and heterozygous genetic models, comparing the GD group and the control group, the combined OR was 1.81, 95% CI [1.56, 2.09]; 1.91, 95% CI [1.66, 2.21]; 2.75, 95% CI, [2.21, 3.41]; and 1.49, 95% CI [1.29, 1.71], respectively. When it was analyzed by dividing genetic models into subgroups according to ethnicity and published year, the data the of genetic model in each subgroup were also statistically significant.

CONCLUSION

The CTLA-4 +49A/G polymorphism was strongly associated with genetic susceptibility to GD. Allele G, genotypes GG, GG + GA, and GA are correlated with an increase in the risk of GD.

摘要

未加标签

细胞毒性 T 淋巴细胞相关抗原 4(CTLA-4)在格雷夫斯病(GD)的发生和发展中起着重要作用,尤其是 CTLA-4+49A/G 多态性和遗传易感性与 GD 相关。然而,目前的结论并不一致。因此,本研究采用荟萃分析方法来评估该多态性与 GD 风险的确切相关性。

方法

在 PubMed、Embase、Web of Science、中国知网、万方等数据库中检索 CTLA-4+49A/G 多态性与 GD 风险相关性的相关文献,文献发表时间截至 2020 年 5 月。采用 Stata 15.0 软件进行数据分析。

结果

共纳入 33 篇文献,包含 8555 例病例和 9533 例对照。结果显示,与 CTLA-4+49 等位基因 A 相比,等位基因 G 的优势比(OR)为 1.62,95%可信区间(95%CI)为[1.56, 2.09]。在显性、隐性、纯合和杂合遗传模型中,将 GD 组与对照组进行比较,合并 OR 分别为 1.81(95%CI[1.56, 2.09])、1.91(95%CI[1.66, 2.21])、2.75(95%CI[2.21, 3.41])和 1.49(95%CI[1.29, 1.71])。根据种族和发表年份将遗传模型分为亚组进行分析时,各亚组遗传模型的数据也均有统计学意义。

结论

CTLA-4+49A/G 多态性与 GD 的遗传易感性密切相关。等位基因 G、基因型 GG、GG+GA 和 GA 与 GD 风险增加相关。

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