Department of Pediatrics, Childhood Asthma Atopy Center, Humidifier Disinfectant Health Center, Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea.
Asan Institute for Life Science, Asan Medical Center, Ulsan University College of Medicine, Seoul, South Korea.
Pediatr Allergy Immunol. 2021 Oct;32(7):1445-1454. doi: 10.1111/pai.13531. Epub 2021 May 21.
Although atopic dermatitis (AD) is associated with certain gene variants, the rapidly increasing incidence of AD suggests that environmental factors contribute to disease development. In this study, we investigated the association of AD incidence and phenotype with antibiotic exposure within 6 months of age, considering the dose administered and genetic risk.
This study included 1637 children from the COCOA cohort. Pediatric allergists assessed the presence of AD at each visit and obtained information about antibiotic exposure for more than 3 days. IL-13 (rs20541) polymorphism was genotyped by the TaqMan method. We stratified the AD phenotypes into four groups and used multinomial logistic regression models for analysis.
Antibiotic exposure within 6 months of age was found to increase the risk of AD within 3 years of life (aOR = 1.40; 95% CI, 1.09-1.81) in dose-dependent manner. Antibiotic exposure more than twice increased the risk of the early-persistent AD phenotype (aOR = 2.50; 95% CI, 1.35-4.63). There was a weak interaction between genetic polymorphisms and environmental factors on the development of AD (p for interaction = 0.06). Children with the IL-13 (rs20541) GA + AA genotype have a higher risk of the early-persistent AD phenotype when exposed to antibiotics more than twice than those with the IL-13 (rs20541) GG genotype and without exposure to antibiotics (aOR = 4.73; 95% CI, 2.01-11.14).
Antibiotic exposure within 6 months was related to the incidence of early-persistent AD and a dose-dependent increase in the incidence of AD in childhood, whose effect was modified by the IL-13 (rs20541) genotype.
尽管特应性皮炎(AD)与某些基因变异有关,但 AD 的发病率迅速上升表明环境因素也有助于疾病的发展。在这项研究中,我们研究了在 6 个月内使用抗生素与 AD 发病和表型的相关性,同时考虑了给药剂量和遗传风险。
这项研究包括 COCOA 队列中的 1637 名儿童。儿科过敏专家在每次就诊时评估 AD 的存在,并获得了超过 3 天的抗生素暴露信息。采用 TaqMan 方法对 IL-13(rs20541)多态性进行基因分型。我们将 AD 表型分为四组,并使用多项逻辑回归模型进行分析。
在生命的头 3 年内,6 个月内使用抗生素会增加 AD 的发病风险(优势比[aOR] = 1.40;95%置信区间[CI],1.09-1.81),呈剂量依赖性。抗生素暴露超过两倍会增加早发性持续性 AD 表型的发病风险(aOR = 2.50;95%CI,1.35-4.63)。遗传多态性和环境因素在 AD 发病中的相互作用较弱(p 交互= 0.06)。与未暴露于抗生素的 IL-13(rs20541)GG 基因型儿童相比,IL-13(rs20541)GA+AA 基因型儿童在暴露于抗生素超过两倍时,早发性持续性 AD 表型的发病风险更高(aOR = 4.73;95%CI,2.01-11.14)。
6 个月内使用抗生素与早发性持续性 AD 的发病有关,并且与儿童期 AD 发病率呈剂量依赖性增加,其作用受 IL-13(rs20541)基因型的调节。