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A Pilot Study of Host Genetic Variants Associated with Influenza-associated Deaths among Children and Young Adults

机译:儿童和年轻人中与流感相关的死亡相关的宿主遗传变异的初步研究

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摘要

We compared the prevalence of 8 polymorphisms in the tumor necrosis factor and mannose-binding lectin genes among 105 children and young adults with fatal influenza with US population estimates and determined in subanalyses whether these polymorphisms were associated with sudden death and bacterial co-infection among persons with fatal influenza. No differences were observed in genotype prevalence or minor allele frequencies between persons with fatal influenza and the reference sample. Fatal cases with low-producing MBL2 genotypes had a 7-fold increased risk for invasive methicillin-resistant Staphylococcus aureus (MRSA) co-infection compared with fatal cases with high- and intermediate-producing MBL2 genotypes (odds ratio 7.1, 95% confidence interval 1.6–32.1). Limited analysis of 2 genes important to the innate immune response found no association between genetic variants and fatal influenza infection. Among children and young adults who died of influenza, low-producing MBL2 genotypes may have increased risk for MRSA co-infection.
机译:我们比较了美国人群估计的105例致命流感儿童和年轻人中肿瘤坏死因子和甘露糖结合凝集素基因中8个多态性的患病率,并在亚分析中确定了这些多态性是否与人的突然死亡和细菌共感染有关致命的流感。致命流感患者和参考样本之间在基因型流行率或次要等位基因频率上未观察到差异。与高和中等生产MBL2基因型的致命病例相比,具有低生产MBL2基因型的致命病例侵袭性耐甲氧西林金黄色葡萄球菌(MRSA)合并感染的风险增加了7倍(优势比为7.1,95%置信区间1.6–32.1)。对先天免疫反应重要的2个基因的有限分析发现,遗传变异与致命流感感染之间没有关联。在死于流感的儿童和年轻人中,低产MBL2基因型可能增加了MRSA合并感染的风险。

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