Lee Eun, Kim Ju Hee, Ha Eun Kyo, Shin Jeewon, Han Bo Eun, Baek Hey Sung, Han Man Yong
Department of Pediatrics, Chonnam National University Hospital, Chonnam National University Medical School, Gwangju, Korea.
Department of Pediatrics, Kyung Hee University Medical Center, Kyung Hee University College of Medicine, Seoul, Korea.
Allergy Asthma Immunol Res. 2024 Sep;16(5):490-504. doi: 10.4168/aair.2024.16.5.490.
Wheezing in early life is most frequently caused by viral lower respiratory tract illnesses, constituting a significant disease burden in children. This study aimed to investigate the association of wheezing in early life with autoimmune diseases throughout childhood.
A population-matched retrospective cohort study was conducted in Korea between 2002 and 2017. The cohort comprised 34,959 children admitted with viral wheezing before 2 years of age and an equal number of the matched unexposed children born in 2002 and 2003. Exposed infants were defined as those hospitalized for bronchiolitis or bronchial asthma before the age of 2. Unexposed controls were matched by sex and birth year at a 1:1 ratio, using incidence density sampling. A Cox proportional hazard model controlled for multiple risk factors was employed.
The median age at hospitalization for wheeze was 9 months (interquartile range, 5-15 months), and 63% of the exposed infants were male. Over the mean 15-year follow-up period, the incidence rate of autoimmune diseases was 74.0 and 62.2 per 10,000 person-years in the exposed and matched unexposed cohorts, respectively. The adjusted hazard ratio for any autoimmune disease in the exposed cohort was 1.15 (95% confidence interval, 1.09-1.23) in comparison with the unexposed cohort. The exposed cohort revealed an augmented risk for specific autoimmune diseases, including juvenile idiopathic arthritis, Kawasaki disease, Henoch-Schönlein purpura, psoriasis, idiopathic thrombocytopenic purpura, and immunoglobulin A nephropathy. Risks were heightened for children with multiple wheezing episodes or a persistent wheezing episode after the age of 2 years.
This research identifies associations between early-life wheeze and the development of autoimmune diseases in childhood. Understanding these relationships can aid in recognizing the underlying pathophysiology of early-life wheeze and childhood autoimmune diseases, contributing to management strategies for these conditions.
生命早期的喘息最常见于病毒性下呼吸道疾病,给儿童带来了重大疾病负担。本研究旨在调查生命早期喘息与儿童期自身免疫性疾病之间的关联。
2002年至2017年在韩国进行了一项人群匹配的回顾性队列研究。该队列包括34959名2岁前因病毒性喘息入院的儿童以及数量相等的2002年和2003年出生的匹配未暴露儿童。暴露婴儿定义为2岁前因细支气管炎或支气管哮喘住院的婴儿。未暴露对照组按性别和出生年份以1:1比例匹配,采用发病密度抽样。采用控制多个危险因素的Cox比例风险模型。
喘息住院的中位年龄为9个月(四分位间距,5 - 15个月),63%的暴露婴儿为男性。在平均15年的随访期内,暴露队列和匹配的未暴露队列中自身免疫性疾病的发病率分别为每10000人年74.0例和62.2例。与未暴露队列相比,暴露队列中任何自身免疫性疾病的调整后风险比为1.15(95%置信区间,1.09 - 1.23)。暴露队列显示特定自身免疫性疾病的风险增加,包括幼年特发性关节炎、川崎病、过敏性紫癜、银屑病、特发性血小板减少性紫癜和免疫球蛋白A肾病。2岁后有多次喘息发作或持续性喘息发作的儿童风险更高。
本研究确定了生命早期喘息与儿童期自身免疫性疾病发生之间的关联。了解这些关系有助于认识生命早期喘息和儿童期自身免疫性疾病的潜在病理生理学,为这些疾病的管理策略提供依据。