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首页> 外文期刊>Epidemiology and infection >Importance of case age in the purported association between phylogenetics and hemolytic uremic syndrome in Escherichia coli O157:H7 infections
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Importance of case age in the purported association between phylogenetics and hemolytic uremic syndrome in Escherichia coli O157:H7 infections

机译:在大肠杆菌O157:H7感染的系统发育和溶血尿毒综合征之间据称有病例年龄的重要性

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Escherichia coli O157:H7 is the largest cause of hemolytic uremic syndrome (HUS). Previous studies proposed that HUS risk varies across the E. coli O157:H7 phylogenetic tree (hypervirulent clade 8), but the role of age in the association is unknown. We determined phylogenetic lineage of E. coli O157:H7 isolates from 1160 culture-confirmed E. coli O157:H7 cases reported in Washington State, 2004–2015. Using generalised estimating equations, we tested the association between phylogenetic lineage and HUS. Age was evaluated as an effect modifier. Among 1082 E. coli O157:H7 cases with both phylogenetic lineage and HUS status (HUS n = 76), stratified analysis suggested effect modification by age. Lineages IIa and IIb, relative to Ib, did not appear associated with HUS in children 0–9-years-old. For cases 10–59-years-old, lineages IIa and IIb appeared to confer increased risk of HUS, relative to lineage Ib. The association reversed in ?60-year-olds. Results were similar for clade 8. Phylogenetic lineage appears to be associated with HUS risk only among those ?10-years-old. Among children 10, the age group most frequently affected, lineage does not explain progression to HUS. However, lineage frequency varied across age groups, suggesting differences in exposure and/or early disease manifestation.
机译:大肠杆菌O157:H7是溶血性尿毒症综合征(HUS)的最大原因。先前的研究表明,HUS风险在整个大肠杆菌O157:H7系统发育树(高毒进化枝8)中有所不同,但年龄在关联中的作用尚不清楚。我们确定了华盛顿州2004-2015年报告的1160例经培养确认的O157:H7大肠杆菌的O157:H7分离株的系统谱。使用广义估计方程,我们测试了系统谱系和HUS之间的关联。年龄被评估为效果调节剂。在1082例同时具有系统谱系和HUS状态(HUS n = 76)的大肠杆菌O157:H7病例中,分层分析表明该效应随年龄而改变。相对于Ib,IIa和IIb世系与0-9岁儿童的HUS无关。对于10-59岁的病例,IIa和IIb世系相对于Ib世系似乎具有更高的HUS风险。该协会在60岁的人群中发生了逆转。进化枝8的结果相似。系统发育谱系似乎仅与那些10岁的人有关HUS风险。在受影响最频繁的年龄段的儿童10中,血统不能解释其进展为HUS。但是,谱系频率随年龄段而变化,表明暴露和/或早期疾病表现存在差异。

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