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Fine mapping of genetic polymorphisms of pulmonary tuberculosis within chromosome 18q11.2 in the Chinese population: a case-control study

机译:中国人群18q11.2号染色体上肺结核遗传多态性的精细定位:病例对照研究

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Background Recently, one genome-wide association study identified a susceptibility locus of rs4331426 on chromosome 18q11.2 for tuberculosis in the African population. To validate the significance of this susceptibility locus in other areas, we conducted a case-control study in the Chinese population. Methods The present study consisted of 578 cases and 756 controls. The SNP rs4331426 and other six tag SNPs in the 100 Kbp up and down stream of rs4331426 on chromosome 18q11.2 were genotyped by using the Taqman-based allelic discrimination system. Results As compared with the findings from the African population, genetic variation of the SNP rs4331426 was rare among the Chinese. No significant differences were observed in genotypes or allele frequencies of the tag SNPs between cases and controls either before or after adjusting for age, sex, education, smoking, and drinking history. However, we observed strong linkage disequilibrium of SNPs. Constructed haplotypes within this block were linked the altered risks of tuberculosis. For example, in comparison with the common haplotype AA(rs8087945-rs12456774), haplotypes AG(rs8087945-rs12456774) and GA(rs8087945-rs12456774) were associated with a decreased risk of tuberculosis, with the adjusted odds ratio(95% confidence interval) of 0.34(0.27-0.42) and 0.22(0.16-0.29), respectively. Conclusions Susceptibility locus of rs4331426 discovered in the African population could not be validated in the Chinese population. None of genetic polymorphisms we genotyped were related to tuberculosis in the single-point analysis. However, haplotypes on chromosome 18q11.2 might contribute to an individual's susceptibility. More work is necessary to identify the true causative variants of tuberculosis.
机译:背景技术最近,一项全基因组关联研究确定了在18q11.2染色体上的rs4331426在非洲人群中的结核易感性基因座。为了验证此易感性基因座在其他地区的重要性,我们在中国人群中进行了病例对照研究。方法本研究共纳入578例和756例对照。使用基于Taqman的等位基因识别系统对rs1831426上下游100 Kbp上游和下游100 Kbp的SNP rs4331426和其他六个标签SNP进行基因分型。结果与非洲人群的调查结果相比,SNP rs4331426的遗传变异在中国人中很少见。在调整年龄,性别,受教育程度,吸烟和饮酒史之前或之后,病例与对照之间在标签SNPs的基因型或等位基因频率上均未观察到显着差异。但是,我们观察到SNP的强烈连锁不平衡。在该区域内构建的单倍型与结核病风险的改变有关。例如,与常见的单体型AA (rs8087945-rs12456774)相比,单体型AG (rs8087945-rs12456774)和GA (rs8087945-rs12456774)与降低结核病风险有关,调整后的优势比(95%置信区间)分别为0.34(0.27-0.42)和0.22(0.16-0.29)。结论在非洲人群中发现的rs4331426易感性基因座在中国人群中无法得到验证。在单点分析中,我们进行基因分型的遗传多态性均与结核病无关。但是,染色体18q11.2上的单倍型可能会影响个体的易感性。要确定结核病的真正致病变异,还需要做更多的工作。

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