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关联研究表明,白细胞介素8基因多态性对支气管哮喘和呼吸道合胞病毒细支气管炎具有相反的影响。

Association study suggests opposite effects of polymorphisms within IL8 on bronchial asthma and respiratory syncytial virus bronchiolitis.

作者信息

Heinzmann Andrea, Ahlert Iris, Kurz Thorsten, Berner Reinhard, Deichmann Klaus A

机构信息

University Children's Hospital, University of Freiburg, 79106 Freiburg, Germany.

出版信息

J Allergy Clin Immunol. 2004 Sep;114(3):671-6. doi: 10.1016/j.jaci.2004.06.038.

Abstract

BACKGROUND

IL-8 is a strong inductor of inflammation. Accordingly, it plays a pivotal role in acute inflammatory responses during respiratory syncytial virus (RSV) infections and in chronic inflammatory diseases such as bronchial asthma and juvenile idiopathic arthritis. Recently, 2 studies have found association of the polymorphism -251A of IL8 with RSV bronchiolitis. Furthermore, epidemiologic studies have demonstrated an increased risk for the development of asthma after RSV bronchiolitis, and a common genetic background for the 2 diseases is currently being discussed.

OBJECTIVE

This study investigated whether IL-8 is in association with asthma and/or arthritis and whether the results can confirm a common genetic background of RSV bronchiolitis and asthma.

METHODS

The polymorphisms -A251T, C781T, C1633T, and A2767T within IL8 were genotyped in the following 4 populations: children with asthma, atopic children, children with juvenile idiopathic arthritis, and control subjects. Statistical analysis made use of the Armitage trend test and the software program Arlequine.

RESULTS

Association of all polymorphisms was found with asthma ( P =.008 to P =.03). Surprisingly -251T was associated with asthma, which is the opposite allele as described in association with RSV bronchiolitis. Furthermore, all polymorphisms were significantly more common in children with arthritis than in asthmatic children ( P =.006 to P =.02). No association was seen with the diagnosis of arthritis per se or with atopy.

CONCLUSION

This is the first study to describe association of IL-8 with asthma and a significant inverse distribution of the polymorphisms in juvenile idiopathic arthritis. In addition, the results of this study might suggest that RSV bronchiolitis and bronchial asthma have at least some different genetic factors.

摘要

背景

白细胞介素-8(IL-8)是一种强大的炎症诱导因子。因此,它在呼吸道合胞病毒(RSV)感染期间的急性炎症反应以及支气管哮喘和幼年特发性关节炎等慢性炎症性疾病中起关键作用。最近,两项研究发现IL8基因-251A多态性与RSV细支气管炎有关。此外,流行病学研究表明,RSV细支气管炎后哮喘发病风险增加,目前正在探讨这两种疾病的共同遗传背景。

目的

本研究调查IL-8是否与哮喘和/或关节炎相关,以及结果是否能证实RSV细支气管炎和哮喘的共同遗传背景。

方法

对以下4组人群的IL8基因中的-A251T、C781T、C1633T和A2767T多态性进行基因分型:哮喘儿童、特应性儿童、幼年特发性关节炎儿童和对照组。统计分析采用阿米蒂奇趋势检验和Arlequine软件程序。

结果

发现所有多态性均与哮喘相关(P = 0.008至P = 0.03)。令人惊讶的是,-251T与哮喘相关,这与RSV细支气管炎相关的等位基因相反。此外,所有多态性在关节炎儿童中比哮喘儿童中显著更常见(P = 0.006至P = 0.02)。未发现与关节炎本身的诊断或特应性相关。

结论

这是第一项描述IL-8与哮喘相关以及幼年特发性关节炎中多态性显著反向分布的研究。此外,本研究结果可能表明RSV细支气管炎和支气管哮喘至少有一些不同的遗传因素。

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