Kurukulaaratchy Ramesh J, Matthews Sharon, Arshad S Hasan
The David Hide Asthma & Allergy Research Centre, St Mary's Hospital, Newport, Isle of Wight, England.
Ann Allergy Asthma Immunol. 2006 Jul;97(1):84-91. doi: 10.1016/S1081-1206(10)61375-0.
The nature of the relationship between childhood wheeze and atopy remains uncertain.
To characterize childhood wheeze among atopic phenotypes in a longitudinal birth cohort study.
A whole population birth cohort (N = 1,456) was recruited in 1989. Children were seen at birth and at 1, 2, 4, and 10 years of age to obtain information on asthma and allergic disease development and relevant risk factors for these states. Skin prick testing at ages 4 (n = 980) and 10 (n = 1,036) years was used to define atopic phenotypes. Wheezing in these states was characterized, and logistic regression was used to identify independent risk factors for wheeze onset in different atopic phenotypes.
Wheeze ever occurred in 37% of never atopics, 38% of early childhood atopics, 65% of chronic childhood atopics, and 52% of delayed childhood atopics. Chronic childhood atopics had significant wheezing morbidity and bronchial hyperresponsiveness. Their wheezing was associated with male sex, early eczema, family history of eczema, and early tobacco exposure. Never atopic wheeze was related to maternal asthma, parental smoking, and respiratory tract infections. Exclusive breastfeeding protected against early childhood atopic wheeze. Maternal asthma, family history of urticaria, and dog ownership increased delayed childhood atopic wheeze.
In many respects, chronic childhood atopy is the atopic phenotype associated with the most significant forms of childhood wheezing. In such children, heritable drive, allergens, and synergy with other environmental triggers seem to be crucial determinants of wheeze onset. Where such sensitization is absent, numerous environmental factors plus genetic predisposition may assume importance for wheezing.
儿童喘息与特应性之间关系的本质仍不明确。
在一项纵向出生队列研究中,对特应性表型中的儿童喘息进行特征描述。
1989年招募了一个全人群出生队列(N = 1456)。在出生时以及1岁、2岁、4岁和10岁时对儿童进行观察,以获取有关哮喘和过敏性疾病发展以及这些疾病相关危险因素的信息。使用4岁(n = 980)和10岁(n = 1036)时的皮肤点刺试验来定义特应性表型。对这些状态下的喘息进行特征描述,并使用逻辑回归来确定不同特应性表型中喘息发作的独立危险因素。
37%的非特应性儿童、38%的儿童早期特应性患者、65%的儿童慢性特应性患者和52%的儿童迟发性特应性患者曾出现喘息。儿童慢性特应性患者有显著的喘息发病率和支气管高反应性。他们的喘息与男性、早期湿疹、湿疹家族史以及早期接触烟草有关。非特应性儿童喘息与母亲哮喘、父母吸烟和呼吸道感染有关。纯母乳喂养可预防儿童早期特应性喘息。母亲哮喘、荨麻疹家族史和养狗增加儿童迟发性特应性喘息。
在许多方面,儿童慢性特应性是与最严重形式的儿童喘息相关的特应性表型。在这类儿童中,遗传驱动、过敏原以及与其他环境触发因素的协同作用似乎是喘息发作的关键决定因素。在不存在这种致敏的情况下,众多环境因素加上遗传易感性可能对喘息起重要作用。