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婴儿严重人细小病毒感染及年长同胞的作用。

Severe Human Parechovirus Infections in Infants and the Role of Older Siblings.

作者信息

Nielsen Nete Munk, Midgley Sofie Elisabeth, Nielsen Alex Christian Yde, Christiansen Claus Bohn, Fischer Thea Kølsen

出版信息

Am J Epidemiol. 2016 Apr 1;183(7):664-70. doi: 10.1093/aje/kwv206. Epub 2016 Mar 10.

DOI:10.1093/aje/kwv206
PMID:26968944
Abstract

Human parechovirus (HPeV) is a cause of severe morbidity among infants and young children. To evaluate the associations between early environmental risk factors and HPeV infections, we carried out a nationwide cohort study linking registry data on birth and sibship characteristics with a laboratory surveillance database, covering all HPeV infections detected in Denmark during 2009-2012 among children <5 years of age. Incidence rate ratios were calculated in log-linear Poisson regression analyses. Overall, 133 HPeV infections, 85 caused by human parechovirus type 3 (HPeV-3) and 48 by human parechovirus other than type 3 (non-HPeV-3), were detected among 132 children. Neither birth weight, mode of delivery, Apgar score, nor gestational age was associated with the risk of HPeV infections. Compared with firstborn children, secondborn children were at a 9-fold increased risk (incidence rate ratio = 8.68, 95% confidence interval: 3.85, 19.53) of contracting HPeV-3 infections, but at no increased risk of contracting non-HPeV-3 infections. However, the shorter the age gap to the nearest older sibling, the higher the risk of HPeV-3 as well as non-HPeV-3 infections, although the trend was strongest for HPeV-3 infections. Our study is the first to suggest that having a slightly older sibling increases the risk for severe neonatal HPeV infections. This new knowledge might lead to new preventive measures.

摘要

人细小病毒(HPeV)是婴幼儿严重发病的一个病因。为了评估早期环境危险因素与HPeV感染之间的关联,我们开展了一项全国性队列研究,将出生和同胞关系特征的登记数据与一个实验室监测数据库相链接,该数据库涵盖了2009年至2012年丹麦5岁以下儿童中检测到的所有HPeV感染病例。在对数线性泊松回归分析中计算发病率比。总体而言,在132名儿童中检测到133例HPeV感染,其中85例由3型人细小病毒(HPeV-3)引起,48例由3型以外的人细小病毒(非HPeV-3)引起。出生体重、分娩方式、阿氏评分和胎龄均与HPeV感染风险无关。与头胎儿童相比,二胎儿童感染HPeV-3的风险增加了9倍(发病率比=8.68,95%置信区间:3.85,19.53),但感染非HPeV-3的风险没有增加。然而,与最近的哥哥或姐姐的年龄差距越短,感染HPeV-3和非HPeV-3的风险就越高,尽管这种趋势在HPeV-3感染中最为明显。我们的研究首次表明,有一个稍大一点的兄弟姐妹会增加新生儿严重HPeV感染的风险。这一新知识可能会带来新的预防措施。

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