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P2X7基因多态性与结核病易感性的荟萃分析。

Metaanalysis of P2X7 gene polymorphisms and tuberculosis susceptibility.

作者信息

Xiao Jing, Sun Lin, Yan Huimin, Jiao Weiwei, Miao Qing, Feng Weixing, Wu Xirong, Gu Yi, Jiao Anxia, Guo Yajie, Peng Xiaoxia, Shen Adong

机构信息

Beijing Pediatric Institute, Beijing Children's Hospital affiliated to Capital Medical University, Beijing, China.

出版信息

FEMS Immunol Med Microbiol. 2010 Nov;60(2):165-70. doi: 10.1111/j.1574-695X.2010.00735.x. Epub 2010 Sep 16.

Abstract

Although many case-control studies have investigated the association between P2X7 gene polymorphisms and tuberculosis susceptibility, the interpretation of these data has been difficult due to limited power. As a means of better understanding the link between P2X7 and tuberculosis, a systematic review of the literature was conducted using metaanalysis. This approach provided a quantitative summary estimate on the association between P2X7 and tuberculosis. We searched databases (MEDLINE, PUBMED, and OVID) between January 1998 and July 2010 using the search words 'gene' or 'P2X7' in combination with 'tuberculosis,' performed manual citation searches from relevant original studies and review articles and corresponded with researchers in the field of study. The pooled odds ratios (ORs) for studies examining variations in the P2X7 gene 1513 C and -762 C loci were 1.44 [95% confidence interval (CI) 1.23-1.68; P<0.00001] and 1.01 (95% CI 0.70-1.44; P=0.97), respectively, compared with the 1513 A and -762 T alleles. Polymorphisms at the 1513 locus had a statistically significant association with P2X7 variants and tuberculosis susceptibility, while the -762 locus allele variants were not significantly associated with P2X7 variants and tuberculosis susceptibility.

摘要

尽管许多病例对照研究调查了P2X7基因多态性与结核病易感性之间的关联,但由于检验效能有限,这些数据的解读一直很困难。作为更好地理解P2X7与结核病之间联系的一种方法,我们使用荟萃分析对文献进行了系统综述。这种方法对P2X7与结核病之间的关联提供了定量的汇总估计。我们在1998年1月至2010年7月期间搜索了数据库(MEDLINE、PUBMED和OVID),使用搜索词“基因”或“P2X7”并结合“结核病”,对相关原始研究和综述文章进行了手动文献检索,并与该研究领域的研究人员进行了通信。与1513A和-762T等位基因相比,检测P2X7基因1513C和-762C位点变异的研究的合并比值比(OR)分别为1.44[95%置信区间(CI)1.23-1.68;P<0.00001]和1.01(95%CI 0.70-1.44;P=0.97)。1513位点的多态性与P2X7变异和结核病易感性具有统计学显著关联,而-762位点的等位基因变异与P2X7变异和结核病易感性无显著关联。

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