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NFKBIZ 多态性与欧洲和非洲人群中肺炎球菌病的易感性。

NFKBIZ polymorphisms and susceptibility to pneumococcal disease in European and African populations.

机构信息

Immunity and Inflammation, The Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.

出版信息

Genes Immun. 2010 Jun;11(4):319-25. doi: 10.1038/gene.2009.76. Epub 2009 Oct 1.

Abstract

The proinflammatory transcription factor nuclear factor-kappaB (NF-kappaB) has a central role in host defence against pneumococcal disease. Both rare mutations and common polymorphisms in the NFKBIA gene encoding the NF-kappaB inhibitor, IkappaB-alpha, associate with susceptibility to bacterial disease, but the possible role of polymorphisms within the related IkappaB-zeta gene NFKBIZ in the development of invasive pneumococcal disease (IPD) has not been reported previously. To investigate this further, we examined the frequencies of 22 single-nucleotide polymorphisms spanning NFKBIZ in two case-control studies, comprising UK Caucasian (n=1008) and Kenyan (n=723) individuals. Nine polymorphisms within a single UK linkage disequilibrium (LD) block and all four polymorphisms within the equivalent, shorter Kenyan LD block displayed either a significant association with IPD or a trend towards association. For each polymorphism, heterozygosity was associated with protection from IPD when compared with the combined homozygous states (for example, for rs600718, Mantel-Haenszel 2 x 2 chi(2)=7.576, P=0.006, odds ratio (OR)=0.67, 95% confidence interval (95% CI) for OR: 0.51-0.88; for rs616597, Mantel-Haenszel 2 x 2 chi(2)=8.715, P=0.003, OR=0.65, 95% CI: 0.49-0.86). We conclude that multiple NFKBIZ polymorphisms associate with susceptibility to IPD in humans. The study of multiple populations may aid in fine mapping of associations within extensive regions of strong LD ('transethnic mapping').

摘要

促炎转录因子核因子-κB(NF-κB)在宿主防御肺炎球菌病中起核心作用。编码 NF-κB 抑制剂 IkappaB-α 的 NFKBIA 基因的罕见突变和常见多态性与细菌病易感性相关,但先前尚未报道相关的 IkappaB-zeta 基因 NFKBIZ 内的多态性在侵袭性肺炎球菌病(IPD)发展中的可能作用。为了进一步研究这一点,我们在两项病例对照研究中检查了横跨 NFKBIZ 的 22 个单核苷酸多态性的频率,包括英国白种人(n=1008)和肯尼亚人(n=723)个体。在一个英国连锁不平衡(LD)块内的 9 个多态性和在等效的更短的肯尼亚 LD 块内的所有 4 个多态性都显示出与 IPD 的显著关联或与关联的趋势。对于每个多态性,与组合的纯合状态相比,杂合性与 IPD 的保护相关(例如,对于 rs600718,Mantel-Haenszel 2 x 2 chi(2)=7.576,P=0.006,优势比(OR)=0.67,95%置信区间(95%CI)为 OR:0.51-0.88;对于 rs616597,Mantel-Haenszel 2 x 2 chi(2)=8.715,P=0.003,OR=0.65,95%CI:0.49-0.86)。我们得出结论,多个 NFKBIZ 多态性与人类 IPD 的易感性相关。对多个群体的研究可能有助于在强 LD (“跨种族映射”)的广泛区域内精细映射关联。

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