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Mutations associated with severity of the pandemic influenza A(HlNl)pdm09 in humans: a systematic review and meta-analysis of epidemiological evidence

机译:与人类大流行性流感A(H1N1)pdm09严重程度相关的突变:流行病学证据的系统回顾和荟萃分析

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Mutations in the haemagglutinin (HA), non-structural protein 1 (NS1) and polymerase basic protein 2 (PB2) of influenza viruses have been associated with virulence. This study investigated the association between mutations in these genes in influenza A(HlNl)pdmO9 virus and the risk of severe or fatal disease. Searches were conducted on the MEDLINE, EMBASE and Web of Science electronic databases and the reference lists of published studies. The PRISMA and STROBE guidelines were followed in assessing the quality of studies and writing-up. Eighteen (18) studies, from all continents, were included in the systematic review (recruiting patients 0-77 years old). The mutation D222G was associated with a significant increase in severe disease (pooled RD: 11 %, 95 % CI: 3.0 % - 18.0 %, p = 0.004) and the risk of fatality (RD: 23 %, 95 % CI: 14.0 %-31.0 %, p = < 0.0001). No association was observed between the mutations HA-D222N, D222E, PB2-E627K and NS1-T123V and severe/ fatal disease. The results suggest that no virus quasispecies bearing virulence-conferring mutations in the HA, PB2 and NS1 predominated. However issues of sampling bias, and bias due to uncontrolled confounders such as comorbidi-ties, and viral and bacterial coinfection, should be born inmind. Influenza A viruses should continue to be monitored for the occurrence of virulence-conferring mutations in HA, PB2 and NS1. There are suggestions that respiratory virus coinfections also affect virus virulence. Studies investigating the role of genetic mutations on disease outcome should make efforts to also investigate the role of respiratory virus coinfections.
机译:流感病毒的血凝素(HA),非结构蛋白1(NS1)和聚合酶碱性蛋白2(PB2)中的突变与毒力有关。这项研究调查了A(H1N1)pdmO9流感病毒中这些基因的突变与严重或致命疾病风险之间的关联。搜索在MEDLINE,EMBASE和Web of Science电子数据库以及已发表研究的参考文献清单中进行。在评估研究质量和撰写论文时遵循了PRISMA和STROBE指南。系统评价包括来自全球各大洲的十八(18)个研究(正在招募0-77岁的患者)。 D222G突变与严重疾病的显着增加(合并RD:11%,95%CI:3.0%-18.0%,p = 0.004)和致命风险(RD:23%,95%CI:14.0%)相关-31.0%,p = <0.0001)。在HA-D222N,D222E,PB2-E627K和NS1-T123V突变与严重/致命疾病之间未发现关联。结果表明,在HA,PB2和NS1中,没有带有毒力赋予突变的准类病毒。但是,应当注意采样偏差以及由于不受控制的混杂因素(例如共病)以及病毒和细菌合并感染而引起的偏差问题。应继续监测甲型流感病毒在HA,PB2和NS1中是否存在赋予毒性的突变。有建议认为呼吸道病毒合并感染也会影响病毒的毒性。研究基因突变对疾病结局的作用的研究应努力研究呼吸道病毒合并感染的作用。

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