Univ. Paris Descartes, Sorbonne Paris Cité, EA 4064, Laboratoire Santé Publique et Environnement, Paris, France; Mairie de Paris, Direction de l'Action Sociale, de l'Enfance et de la Santé, Cellule Cohorte, Paris, France.
Allergy. 2013 Sep;68(9):1158-67. doi: 10.1111/all.12208. Epub 2013 Aug 6.
The natural course of childhood asthma and allergy is complex and not fully understood. We aimed to identify phenotypes based upon the time course of respiratory/allergic symptoms throughout preschool years.
As part of the PARIS cohort, symptoms of wheezing, dry night cough, rhinitis and dermatitis were collected annually from birth to age 4 years. K-means clustering was used to group into phenotypes children with similar symptoms trajectories over the study period. Associations of phenotypes with IgE sensitization and risk factors were studied using multinomial logistic regression.
Besides a group with low prevalence of symptoms considered as reference (n = 1236, 49.0%), four distinct respiratory/allergic phenotypes were identified: two transient [transient rhinitis phenotype (n = 295, 11.7%), transient wheeze phenotype (n = 399, 15.8%)], without any relation with IgE sensitization, and two persistent [cough/rhinitis phenotype (n = 284, 11.3%), dermatitis phenotype (n = 308, 12.2%)], associated with IgE sensitization. Transient rhinitis phenotype was only associated with tobacco smoke exposure, which could irritate the airways. Transient wheeze phenotype was related to male sex and contact with other children (older siblings, day care attendance). Lastly, risk factors for both IgE-associated phenotypes encompassed parental history of allergy, potential exposure to allergens and stress, known to be associated with the development of allergic diseases.
This study provides evidence for the existence of different respiratory/allergic phenotypes before school age. The fact that they differ in terms of sensitization and risk factors reinforces the plausibility of distinct phenotypes, potentially linked to irritation and infections for the transient phenotypes and to allergy for the persistent phenotypes.
儿童哮喘和过敏的自然病程复杂,尚未完全阐明。我们旨在根据学龄前儿童呼吸道/过敏症状的时间进程确定表型。
作为 PARIS 队列的一部分,从出生到 4 岁,每年收集喘息、夜间干咳、鼻炎和皮炎的症状。使用 K-均值聚类将具有相似研究期间症状轨迹的儿童分组为表型。使用多项逻辑回归研究表型与 IgE 致敏和危险因素的关联。
除了考虑到发病率较低的症状组(n = 1236,49.0%)作为参考外,还确定了四种不同的呼吸道/过敏表型:两种短暂性表型[短暂性鼻炎表型(n = 295,11.7%)、短暂性喘息表型(n = 399,15.8%)],与 IgE 致敏无关,和两种持续性表型[咳嗽/鼻炎表型(n = 284,11.3%)、皮炎表型(n = 308,12.2%)],与 IgE 致敏相关。短暂性鼻炎表型仅与烟草烟雾暴露有关,这可能会刺激气道。短暂性喘息表型与男性性别和与其他儿童(兄弟姐妹、日托)接触有关。最后,两种 IgE 相关表型的危险因素包括父母过敏史、潜在的过敏原暴露和压力,这些因素与过敏疾病的发展有关。
本研究为学龄前儿童存在不同的呼吸道/过敏表型提供了证据。它们在致敏和危险因素方面存在差异,这进一步证实了不同表型的存在,潜在的表型与短暂表型的刺激和感染有关,与持续表型的过敏有关。