Suppr超能文献

肿瘤坏死因子-α 基因 -308 G/A 多态性与哮喘易感性相关:荟萃分析的更新。

The -308 G/A polymorphism in TNF-α gene is associated with asthma risk: an update by meta-analysis.

机构信息

Department of Respiratory Medicine, West China Hospital of Sichuan University, Chengdu, Sichuan 610041, China.

出版信息

J Clin Immunol. 2011 Apr;31(2):174-85. doi: 10.1007/s10875-010-9477-3. Epub 2010 Nov 17.

Abstract

BACKGROUND

The -308 G/A polymorphism in TNF-α gene has been extensively investigated for association to asthma; however, results of different studies have been inconsistent. The aim of this study is to comprehensively evaluate the genetic risk of -308 G/A polymorphism in TNF-α gene for asthma.

METHODS

A meta-analysis was carried out to analyze the association between the -308 G/A polymorphism TNF-α gene and asthma risk.

RESULTS

A total of 4717 cases and 5012 controls in 29 case-control studies were included in this meta-analysis. The result indicated that the variant A allele carriers had a 38% increased risk of asthma, when compared with the homozygote GG (odds ratio (OR) = 1.40, 95% confidence interval (CI), 1.13-1.68 for AA + AG vs. GG). In the subgroup analysis by ethnicity, significant elevated risks were associated with A allele carriers in Asians (OR = 1.53, 95% CI = 1.17-2.01 and P = 0.002) but not in Caucasians(OR = 1.06, 95% CI = 0.75-1.50 and P = 0.73). In the subgroup analysis by age, significant elevated risks were associated with A allele carriers in adults (OR = 1.44, 95% CI = 1.14-1.81, and P = 0.002) and children (OR = 1.37, 95% CI = 1.03-1.82, and P = 0.003). In the subgroup analysis by atopic status, significant elevated risks of asthma were associated with A allele carriers in atopic population (OR = 1.68, 95% CI = 1.34-2.10, and P < 0.00001) but not in non-atopic population (OR = 0.98, 95% CI = 0.58-1.68, and P = 0.95).

CONCLUSIONS

Our results suggest that the TNF-α -308 G/A polymorphism contributes to susceptibility to asthma.

摘要

背景

TNF-α 基因的-308 G/A 多态性已被广泛研究与哮喘的关联;然而,不同研究的结果并不一致。本研究旨在综合评估 TNF-α 基因-308 G/A 多态性的遗传风险与哮喘的关系。

方法

进行荟萃分析以分析 TNF-α 基因-308 G/A 多态性与哮喘风险的关联。

结果

本荟萃分析共纳入 29 项病例对照研究的 4717 例病例和 5012 例对照。结果表明,与纯合子 GG 相比,变异 A 等位基因携带者患哮喘的风险增加了 38%(比值比(OR)=1.40,95%置信区间(CI)为 1.13-1.68,AA+AG 与 GG 相比)。按种族亚组分析,亚洲人群中 A 等位基因携带者的风险显著升高(OR=1.53,95%CI=1.17-2.01,P=0.002),而高加索人群中未观察到这种相关性(OR=1.06,95%CI=0.75-1.50,P=0.73)。按年龄亚组分析,成人(OR=1.44,95%CI=1.14-1.81,P=0.002)和儿童(OR=1.37,95%CI=1.03-1.82,P=0.003)中 A 等位基因携带者的风险显著升高。按特应性状态亚组分析,特应性人群中哮喘的风险与 A 等位基因携带者显著相关(OR=1.68,95%CI=1.34-2.10,P<0.00001),而非特应性人群中无相关性(OR=0.98,95%CI=0.58-1.68,P=0.95)。

结论

我们的结果表明,TNF-α-308 G/A 多态性与哮喘易感性有关。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验