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肿瘤坏死因子α基因多态性与肺结核易感性相关:一项荟萃分析的证据

Tumor necrosis factor alpha gene polymorphism contributes to pulmonary tuberculosis susceptibility: evidence from a meta-analysis.

作者信息

Yi Yong-Xiang, Han Jian-Bo, Zhao Liang, Fang Yuan, Zhang Yu-Feng, Zhou Guang-Yao

机构信息

Department of Hepatobiliary Surgery, The Second Hospital of Nanjing, Affiliated to Southeast University Nanjing 210003, China.

Department of Immunotherapy, The Second Hospital of Nanjing, Affiliated to Southeast University Nanjing 210003, China.

出版信息

Int J Clin Exp Med. 2015 Nov 15;8(11):20690-700. eCollection 2015.

Abstract

This study is to estimate the association between polymorphisms in the tumor necrosis factor alpha (TNF-α) gene and pulmonary tuberculosis susceptibility (pTB). Studies were identified by searching PubMed and ISI web of Knowledge. The strength of association between the TNF-α gene and pTB susceptibility was assessed by odds ratios. Totals of 18 studies including 2, 735 cases and 3, 177 controls were identified referring to four single-nucleotide polymorphisms: -308G>A, -863C>A, -857C>T and -238G>A. The significantly associations were found between -308G>A (Dominant model: OR 0.53, 95% CI 0.35-0.81, P=0.004; Homozygote model: OR 0.51, 95% CI 0.33-0.78, P=0.002), -238G>A (Dominant model: OR 0.33, 95% CI 0.18-0.57, P<0.001) and pTB susceptibility. The results showed that the variant genotype of TNF-α -308G>A was protective in pooled groups of patients with pTB in the dominant genetic model (OR 0.16, 95% CI 0.06-0.39, P<0.001), the homozygote comparison (OR 0.14, 95% CI 0.06-0.36, P<0.001) in African, while that was with -238G>A in the dominant genetic model (OR 0.31, 95% CI 0.18-0.56, P<0.001) in Asian. Our meta-analysis suggest TNF-α -308G>A and -238G>A polymorphisms increases the risk of pTB susceptibility regardless of ethnicity and HIV statue. In Asian population, the significantly association with pTB is TNF-α -238G>A, while TNF-α -308G>A is in African population.

摘要

本研究旨在评估肿瘤坏死因子α(TNF-α)基因多态性与肺结核易感性(pTB)之间的关联。通过检索PubMed和ISI知识网络来确定相关研究。采用比值比评估TNF-α基因与pTB易感性之间的关联强度。共纳入18项研究,包括2735例病例和3177例对照,涉及四个单核苷酸多态性:-308G>A、-863C>A、-857C>T和-238G>A。发现-308G>A(显性模型:OR 0.53,95%CI 0.35 - 0.81,P = 0.004;纯合子模型:OR 0.51,95%CI 0.33 - 0.78,P = 0.002)、-238G>A(显性模型:OR 0.33,95%CI 0.18 - 0.57,P < 0.001)与pTB易感性之间存在显著关联。结果显示,在显性遗传模型中,TNF-α -308G>A的变异基因型在非洲人群中对合并的肺结核患者组具有保护作用(OR 0.16,95%CI 0.06 - 0.39,P < 0.001),在纯合子比较中(OR 0.14,95%CI 0.06 - 0.36,P < 0.001);而在亚洲人群中,显性遗传模型下与pTB显著相关的是-238G>A(OR 0.31,95%CI 0.18 - 0.56,P < 0.001)。我们的荟萃分析表明,TNF-α -308G>A和-238G>A多态性增加了pTB易感性风险,且不受种族和HIV状态影响。在亚洲人群中,与pTB显著相关的是TNF-α -238G>A,而在非洲人群中是TNF-α -308G>A。

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