Marmarinos Antonios, Saxoni-Papageorgiou Photini, Cassimos Dimitrios, Manoussakis Emmanuel, Tsentidis Charalampos, Doxara Alexia, Paraskakis Irene, Gourgiotis Dimitrios
a Laboratory of Clinical Biochemistry - Molecular Diagnostics, Second Department of Pediatrics , Athens University Medical School, "P & A Kyriakou" Children's Hospital , Athens , Attica , Greece .
J Asthma. 2015;52(6):554-9. doi: 10.3109/02770903.2014.990092. Epub 2015 Jul 8.
Backround: Reliable biological markers for the differentiation of asthma phenotypes in preschool children with wheezing are lacking. The purpose of the study is to assess the relationship of urinary Leukotriene E4 (U-LTE4) to particular asthma phenotypes in preschool children with recurrent episodic (viral) wheezing following upper respiratory tract infections with or without atopic predisposition.
Ninety-six preschool patients with recurrent episodic wheezing participated, 52 atopic and 44 non-atopic, during exacerbation and in remission. Exacerbation was defined on clinical basis (wheeze in the presence of coryzal symptoms). Atopy was determined by specific serum IgE measurement and skin-prick testing. U-LTE4 was determined by enzyme immunoassay. Thirty-six age-matched, non-asthmatic, non-atopic children served as controls.
During exacerbation, U-LTE4 was significantly higher in all children with recurrent episodic wheezing in comparison to A: Remission: 642.20 ± 268 versus 399.45 ± 204, p value <0.001 and B:
642.20 ± 268 versus 271.39 ± 83, p value <0.001. Atopic patients demonstrated significantly higher levels of U-LTE4 compared to non-atopic, both during exacerbation 872.13 ± 246 versus 613.15 ± 150, p value = 0.0013 and during remission 507.59 ± 182 versus 283.59 ± 160, p value <0.001. During remission, a highly significant difference of U-LTE4 was found when controls were compared to atopic patients: 271.39 ± 83 versus 507.59 ± 182, p value = 0.002 but not when compared to non-atopic ones: 271.39 ± 83 versus 283.59 ± 160, p value = 0.432.
U-LTE4 is strongly associated with the acute wheeze episode in preschool children, more so in atopics. Increased basal levels of U-LTE4 occur only in atopics. This suggests a potential role of U-LTE4 as a marker of atopic, virus-induced asthma in preschool children.
背景:缺乏用于区分学龄前喘息儿童哮喘表型的可靠生物标志物。本研究的目的是评估尿白三烯E4(U-LTE4)与学龄前反复发生(病毒性)喘息的儿童在有或无特应性易感性的上呼吸道感染后的特定哮喘表型之间的关系。
96例反复发生喘息的学龄前患者参与研究,其中52例有特应性,44例无特应性,在病情加重期和缓解期进行研究。病情加重根据临床标准定义(伴有鼻卡他症状时出现喘息)。特应性通过特异性血清IgE测量和皮肤点刺试验确定。U-LTE4通过酶免疫测定法测定。36名年龄匹配的非哮喘、非特应性儿童作为对照。
在病情加重期,所有反复发生喘息的儿童的U-LTE4均显著高于A:缓解期:642.20±268对比399.45±204,p值<0.001;B:对照组:642.20±268对比271.39±83,p值<0.001。有特应性的患者在病情加重期(872.13± 246对比613.15±150,p值=0.0013)和缓解期(507.59±182对比283.59±160,p值<0.001)的U-LTE4水平均显著高于无特应性的患者。在缓解期,将对照组与有特应性的患者相比,发现U-LTE4有高度显著差异:271.39±83对比507.59±182,p值=0.002;但与无特应性的患者相比则无差异:271.39±83对比283.59±160,p值=0.432。
U-LTE4与学龄前儿童的急性喘息发作密切相关,在有特应性的儿童中更为明显。U-LTE4的基础水平升高仅发生在有特应性的儿童中。这表明U-LTE4可能作为学龄前儿童特应性、病毒诱导性哮喘的标志物。