Copenhagen Prospective Studies on Asthma in Childhood, Health Sciences, University of Copenhagen, Copenhagen, Denmark
Am J Respir Crit Care Med. 2011 Sep 15;184(6):656-61. doi: 10.1164/rccm.201101-0111OC.
Biomarkers predicting development of atopic disease are needed for targeted preventive measures and to study if disease pathology may be active before onset of symptoms.
To investigate whether eosinophil protein X, leukotriene-C4/D4/E4, and 11β-prostaglandin (PG) F2α (PGD2 metabolite) assessed in urine from healthy at-risk neonates precede development of atopic disease during the first 6 years of life.
We measured eosinophil protein X (n = 369), leukotriene-C4/D4/E4 (n = 367), and 11β-PGF2α (n = 366) in urine from 1-month-old children participating in the Copenhagen Prospective Studies on Asthma in Childhood birth cohort. Clinical data on development of allergic sensitization, allergic rhinitis, nasal eosinophilia, blood eosinophilia, eczema, troublesome lung symptoms (significant cough or wheeze or dyspnea), and asthma were collected prospectively until age 6 years. Associations between urinary biomarkers and development of atopic traits were investigated using general estimating equations, logistic regression, and Cox regression.
Eosinophil protein X in the urine of the asymptomatic 1-month-old neonates was significantly associated with development of allergic sensitization (odds ratio, 1.49; 95% confidence interval [CI], 1.08–1.89), nasal eosinophilia (odds ratio, 3.2; 95% CI, 1.2–8.8), and eczema (hazard ratio, 1.4; 95% CI, 1.0–2.0), but not with allergic rhinitis, asthma, or blood eosinophilia. Neither leukotriene-C4/D4/E4 nor 11β-PGF2α was associated with any of the atopic phenotypes.
Eosinophil protein X in urine from asymptomatic neonates is a biomarker significantly associated with later development of allergic sensitization, nasal eosinophilia, and eczema during the first 6 years of life. These findings suggest activation of eosinophil granulocytes early in life before development of atopy-related symptoms.
需要预测特应性疾病发展的生物标志物,以进行有针对性的预防措施,并研究疾病病理是否可能在出现症状之前就已经活跃。
探讨健康高危新生儿尿液中的嗜酸性粒细胞蛋白 X、白三烯 C4/D4/E4 和 11β-前列腺素(PGD2 代谢物)是否先于生命的头 6 年中发展为特应性疾病。
我们测量了参加哥本哈根儿童哮喘前瞻性研究的 1 个月大儿童尿液中的嗜酸性粒细胞蛋白 X(n = 369)、白三烯 C4/D4/E4(n = 367)和 11β-PGF2α(n = 366)。前瞻性收集了过敏性致敏、过敏性鼻炎、鼻嗜酸性粒细胞增多、血液嗜酸性粒细胞增多、湿疹、肺部问题(显著咳嗽或喘息或呼吸困难)和哮喘的临床数据,直至 6 岁。使用广义估计方程、逻辑回归和 Cox 回归分析尿液生物标志物与特应性特征发展之间的关系。
无症状 1 个月大新生儿尿液中的嗜酸性粒细胞蛋白 X 与过敏性致敏(优势比,1.49;95%置信区间[CI],1.08-1.89)、鼻嗜酸性粒细胞增多(优势比,3.2;95% CI,1.2-8.8)和湿疹(风险比,1.4;95% CI,1.0-2.0)的发展显著相关,但与过敏性鼻炎、哮喘或血液嗜酸性粒细胞增多无关。白三烯 C4/D4/E4 和 11β-PGF2α 均与任何特应性表型无关。
无症状新生儿尿液中的嗜酸性粒细胞蛋白 X 是与生命的头 6 年中过敏性致敏、鼻嗜酸性粒细胞增多和湿疹发展显著相关的生物标志物。这些发现表明,在出现特应性相关症状之前,嗜酸性粒细胞粒细胞就已经在生命早期被激活。