Department of Pediatrics, University of Michigan Health, Ann Arbor, Michigan, USA.
Rho Federal Systems Division, Inc., Durham, North Carolina, USA.
Pediatr Allergy Immunol. 2024 Jul;35(7):e14197. doi: 10.1111/pai.14197.
Viral wheezing is an important risk factor for asthma, which comprises several respiratory phenotypes. We sought to understand if the etiology of early-life wheezing illnesses relates to childhood respiratory and asthma phenotypes.
Data were collected prospectively on 429 children in the Urban Environment and Childhood Asthma (URECA) birth cohort study through age 10 years. We identified wheezing illnesses and the corresponding viral etiology (PCR testing of nasal mucus) during the first 3 years of life. Six phenotypes of respiratory health were identified at 10 years of age based on trajectories of wheezing, allergic sensitization, and lung function. We compared the etiology of early wheezing illnesses to these wheezing respiratory phenotypes and the development of asthma.
In the first 3 years of life, at least one virus was detected in 324 (67%) of the 483 wheezing episodes documented in the study cohort. Using hierarchical partitioning we found that non-viral wheezing episodes accounted for the greatest variance in asthma diagnosed at both 7 and 10 years of age (8.0% and 5.8% respectively). Rhinovirus wheezing illnesses explained the most variance in respiratory phenotype outcome followed by non-viral wheezing episodes (4.9% and 3.9% respectively) at 10 years of age.
Within this high-risk urban-residing cohort in early life, non-viral wheezing episodes were frequently identified and associated with asthma development. Though rhinovirus wheezing illnesses had the greatest association with phenotype outcome, the specific etiology of wheezing episodes in early life provided limited information about subsequent wheezing phenotypes.
病毒性喘息是哮喘的一个重要危险因素,哮喘包含几种呼吸道表型。我们试图了解婴儿早期喘息疾病的病因是否与儿童呼吸道和哮喘表型有关。
通过年龄为 10 岁的 Urban Environment and Childhood Asthma (URECA) 出生队列研究,前瞻性地收集了 429 名儿童的数据。我们在生命的头 3 年中识别出喘息疾病和相应的病毒病因(鼻黏液的 PCR 检测)。根据喘息、过敏致敏和肺功能的轨迹,在 10 岁时确定了 6 种呼吸道健康表型。我们将早期喘息疾病的病因与这些喘息呼吸道表型和哮喘的发展进行了比较。
在研究队列中记录的 483 次喘息发作中,有 324 次(67%)在生命的头 3 年内至少检测到一种病毒。通过分层划分,我们发现非病毒性喘息发作占 7 岁和 10 岁时诊断为哮喘的最大方差(分别为 8.0%和 5.8%)。鼻病毒喘息疾病在呼吸道表型结果方面解释了最大的方差,其次是非病毒性喘息发作(分别为 4.9%和 3.9%)。
在这个生命早期居住在高风险城市的队列中,经常发现非病毒性喘息发作并与哮喘的发展有关。虽然鼻病毒喘息疾病与表型结果的关联最大,但早期喘息发作的具体病因对随后的喘息表型提供的信息有限。