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肿瘤坏死因子α(TNF-α)基因多态性与格雷夫斯病的关联:一项荟萃分析。

Association of tumour necrosis factor alpha (TNF-alpha) polymorphisms with Graves' disease: A meta-analysis.

作者信息

Li Ni, Zhou Zongguang, Liu Xuyang, Liu Yi, Zhang Junjun, Du Liang, Wei Maoling, Chen Xiaoming

机构信息

Department of Ophthalmology, West China Hospital, Sichuan University, Chengdu, China.

出版信息

Clin Biochem. 2008 Jul;41(10-11):881-6. doi: 10.1016/j.clinbiochem.2008.04.014. Epub 2008 Apr 26.

DOI:10.1016/j.clinbiochem.2008.04.014
PMID:18472000
Abstract

OBJECTIVE

To quantitatively summarize the association between tumour necrosis factor alpha (TNF-alpha) gene polymorphisms and Graves' disease.

DESIGN AND METHODS

Relevant studies were identified from the following electronic databases: Cochrane Library, MEDLINE, EMBASE and Chinese Bio-medicine Database. A meta-analysis of relevant studies was performed.

RESULTS

This meta-analysis included 10 case-control studies, which included 2271 Graves' disease cases and 2633 controls. The combined results based on all studies showed that there was significant difference in genotype distribution (-308A/G; -308G/G; -863C/C; -863C/A; -1031C/T) between Graves' disease and controls. When stratifying for race, statistically significant results were observed in three genotype distribution (-863C/C; -863C/A; -1031C/T) between Graves' disease and controls among Asians. Statistically significant results were observed in only two genotype distribution (-308A/G; -308G/G) between Graves' disease and controls among Caucasians.

CONCLUSIONS

This meta-analysis suggests that TNF-alpha gene polymorphisms at positions -308 (G-308A), -863 (C-863A), and -1031 (T-1031C) were associated with Graves' disease.

摘要

目的

定量总结肿瘤坏死因子α(TNF-α)基因多态性与格雷夫斯病之间的关联。

设计与方法

从以下电子数据库中检索相关研究:考克兰图书馆、医学文献数据库、荷兰医学文摘数据库及中国生物医学数据库。对相关研究进行荟萃分析。

结果

该荟萃分析纳入了10项病例对照研究,其中包括2271例格雷夫斯病患者和2633例对照。基于所有研究的合并结果显示,格雷夫斯病与对照之间在基因型分布(-308A/G;-308G/G;-863C/C;-863C/A;-1031C/T)上存在显著差异。按种族分层时,在亚洲人群中,格雷夫斯病与对照之间在三种基因型分布(-863C/C;-863C/A;-1031C/T)上观察到具有统计学意义的结果。在白种人群中,格雷夫斯病与对照之间仅在两种基因型分布(-308A/G;-308G/G)上观察到具有统计学意义的结果。

结论

该荟萃分析表明,位于-308(G-308A)、-863(C-863A)和-1031(T-1031C)位点的TNF-α基因多态性与格雷夫斯病相关。

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