Carra Sophie, Zhang Hongmei, Tanno Luciana Kase, Arshad Syed Hasan, Kurukulaaratchy Ramesh J
Respiratory Biomedical Research Centre, University Hospital Southampton, Southampton SO16 6YD, UK.
The David Hide Asthma and Allergy Research Centre, St Mary's Hospital, Newport, Isle of Wight PO30 5TG, UK.
J Pers Med. 2024 Dec 22;14(12):1171. doi: 10.3390/jpm14121171.
While the phenotypic diversity of childhood wheezing is well described, the subsequent life course of such phenotypes and their adult outcomes remain poorly understood. We hypothesized that different childhood wheezing phenotypes have varying longitudinal outcomes at age 26. We sought to identify factors associated with wheezing persistence, clinical remission, and new onset in adulthood. Methods: Participants were seen at birth and at 1, 2, 4, 10, 18, and 26 years in the Isle of Wight Birth Cohort ( = 1456). Information was collected prospectively on wheeze prevalence and phenotypic characteristics at each assessment. Wheeze phenotypes at 10 years were defined as participants wheezing (CW10) or not wheezing at 10 (CNW10). Multivariable regression analyses were undertaken to identify factors associated with wheezing persistence/remission in CW10 and wheeze development in CNW10 at age 26 years. Childhood wheezing phenotypes showed different subsequent outcomes and associated risk factors. Adult wheeze developed in 17.8% of CNW10. Factors independently associated with adult wheeze development in CNW10 included eczema at age 4 years, family history of rhinitis, and parental smoking at birth. Conversely, 56.1% of CW10 had remission of wheeze by 26 years. Factors predicting adult wheezing remission in CW10 included absence of both atopy at age 4 years and family history of rhinitis. Early-life factors influence adult outcomes for childhood wheezing phenotypes, both with respect to later development of adult wheezing in asymptomatic participants and of wheeze remission in childhood wheezers. This suggests potential areas that could be targeted by early-life interventions to alleviate adult disease burden.
虽然儿童喘息的表型多样性已有充分描述,但这些表型随后的生命历程及其成年后的结局仍知之甚少。我们假设不同的儿童喘息表型在26岁时具有不同的纵向结局。我们试图确定与喘息持续、临床缓解和成年后新发相关的因素。方法:在怀特岛出生队列中,对参与者在出生时以及1岁、2岁、4岁、10岁、18岁和26岁时进行观察(n = 1456)。每次评估时前瞻性收集喘息患病率和表型特征信息。10岁时的喘息表型定义为10岁时喘息的参与者(CW10)或不喘息的参与者(CNW10)。进行多变量回归分析,以确定与26岁时CW10中的喘息持续/缓解以及CNW10中的喘息发展相关的因素。儿童喘息表型显示出不同的后续结局和相关危险因素。17.8%的CNW10成年后出现喘息。与CNW10成年后喘息发展独立相关的因素包括4岁时的湿疹、鼻炎家族史和出生时父母吸烟。相反,56.1%的CW10到26岁时喘息缓解。预测CW10成年后喘息缓解的因素包括4岁时无特应性和无鼻炎家族史。早期生活因素会影响儿童喘息表型的成年结局,无论是在无症状参与者中成年后喘息的后期发展,还是在儿童喘息者中喘息的缓解。这表明早期生活干预可能针对的潜在领域,以减轻成年后的疾病负担。