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Associations Between TNFAIP3 Gene Polymorphisms and Systemic Lupus Erythematosus: A Meta-Analysis

机译:TNFAIP3基因多态性与系统性红斑狼疮之间的关联:荟萃分析。

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Objective: The aim of this study was to determine whether the tumor necrosis factor-alpha-indudble protein 3 (TNFAIP3) polymorphisms confer susceptibility to systemic lupus erythematosus (SLE) in ethnically different populations. Methods: The authors conducted meta-analyses on associations between the TNFAIP3 polymorphisms and SLE susceptibility, using fixed and random effects models. Results: A total of eight comparative studies were included in this meta-analysis, which included four Asian, three European, and one African American population. Meta-analysis revealed that an association was found between the minor allele of rs2230926 and SLE in all subjects (odds ratio [OR] 1.848,95% confidence interval [CI] 1.547-2.208, p< 1.0 × 10~(-9)). After stratification by ethnicity, the minor allele of rs2230926 was found to be significantly associated with SLE in Asians and Europeans (OR 1.821,95% CI 1.495-2.219, p< 1.0×10~(-9); OR 2.251,95% CI 1.830-2.768, p< 1.0× 10~(-9)). In addition, a significant association was found between the minor allele of the rs5029939 polymorphism and the risk of developing SLE in all study subjects and Europeans (OR 1.804, 95% CI 1.255-2.592, p = 0.001; OR 2.145, 95% CI 1.731-2.658, p< 1.0×10~(-9)). Furthermore, an association was found between the minor allele of rs3757173 and SLE in all study subjects (OR 1.540, 95% CI 1.017-2.331, p = 0.041). However, no association was found between SLE susceptibility and rs6922466 (OR 0.953, 95% CI 0.812-1.120, p = 0.561). Conclusions: This meta-analysis confirms that the TNFAIP3 polymorphisms are associated with SLE susceptibility in different ethnic groups, namely in Asians and Europeans.
机译:目的:本研究的目的是确定肿瘤坏死因子-α-不育蛋白3(TNFAIP3)多态性是否赋予不同种族人群系统性红斑狼疮(SLE)易感性。方法:作者使用固定和随机效应模型对TNFAIP3多态性与SLE易感性之间的关联进行了荟萃分析。结果:这项荟萃分析总共包括八项比较研究,其中包括四名亚洲人,三名欧洲人和一个非裔美国人。荟萃分析显示,所有受试者中rs2230926的次要等位基因与SLE之间均存在关联(优势比[OR] 1.848,95%置信区间[CI] 1.547-2.208,p <1.0×10〜(-9)) 。按种族分层后,在亚洲人和欧洲人中发现rs2230926的次要等位基因与SLE显着相关(OR 1.821,95%CI 1.495-2.219,p <1.0×10〜(-9); OR 2.251,95%CI 1.830-2.768,p <1.0×10〜(-9))。此外,在所有研究对象和欧洲人中,rs5029939多态性的次要等位基因与发生SLE的风险之间存在显着关联(OR 1.804,95%CI 1.255-2.592,p = 0.001; OR 2.145,95%CI 1.731 -2.658,p <1.0×10〜(-9))。此外,在所有研究对象中,rs3757173的次要等位基因与SLE之间都存在关联(OR 1.540,95%CI 1.017-2.331,p = 0.041)。但是,未发现SLE易感性与rs6922466之间存在关联(OR 0.953,95%CI 0.812-1.120,p = 0.561)。结论:这项荟萃分析证实,TNFAIP3基因多态性与亚洲人和欧洲人等不同种族的SLE易感性有关。

著录项

  • 来源
    《Genetic testing and molecular biomarkers》 |2012年第9期|p.1105-1110|共6页
  • 作者

    Young Ho Lee; Gwan Gyu Song;

  • 作者单位

    Division of Rheumatology Department of Internal Medicine Korea University Korea University College of Medicine 126-1, Anam-dong 5-ga Seongbuk-gu Seoul 136-705 Korea;

    Division of Rheumatology, Department of Internal Medicine, Korea University College of Medicine, Korea University Medical Center, Seoul, Korea;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
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