1 Dr. von Hauner Children's Hospital, Ludwig Maximilians University Munich, Munich, Germany.
2 Department of Pediatrics, University of California, San Diego, La Jolla, California.
Am J Respir Crit Care Med. 2016 Apr 15;193(8):889-97. doi: 10.1164/rccm.201507-1493OC.
Growing up on a farm protects from childhood asthma and early wheeze. Virus-triggered wheeze in infancy predicts asthma in individuals with a genetic asthma risk associated with chromosome 17q21.
To test environmental determinants of infections and wheeze in the first year of life, potential modifications of these associations by 17q21, and the implications for different trajectories of wheeze.
We followed 983 children in rural areas of Europe from birth until age 6 years. Symptoms of wheeze, rhinitis, fever, and environmental exposures were documented with weekly diaries during year 1. Asthma at age 6 was defined as ever having a reported doctor's diagnosis. Single-nucleotide polymorphisms related to ORMDL3 (rs8076131) and GSDMB (rs7216389, rs2290400) at 17q21 were genotyped.
Early wheeze was positively associated with presence of older siblings among carriers of known asthma risk alleles at 17q21 (e.g., rs8076131) (adjusted odds ratio [aOR], 1.53; 95% confidence interval [CI], 1.16-2.01). Exposure to farm animal sheds was inversely related to wheeze (aOR, 0.44; 95% CI, 0.33-0.60). Both effects were similarly observed in children with transient wheeze up to age 3 years without subsequent development of asthma (aOR, 1.71 [95% CI, 1.09-2.67]; and aOR, 0.48 [95% CI, 0.30-0.76], respectively).
These findings suggest that the chromosome 17q21 locus relates to episodes of acute airway obstruction common to both transient wheeze and asthma. The previously identified asthma risk alleles are the ones susceptible to environmental influences. Thus, this gene-environment interaction reveals two faces of 17q21: The same genotype constitutes genetic risk and allows for environmental protection, thereby providing options for prospective prevention strategies.
在农场长大可预防儿童时期的哮喘和早期喘息。婴儿时期由病毒引发的喘息可预测与 17 号染色体 q21 相关的遗传哮喘风险个体的哮喘。
检测生命第一年中感染和喘息的环境决定因素,17q21 对这些关联的潜在修饰作用,以及对不同喘息轨迹的影响。
我们从出生开始,在欧洲农村地区对 983 名儿童进行了随访,直到 6 岁。在第 1 年中,通过每周日记记录喘息、鼻炎、发热和环境暴露的症状。6 岁时的哮喘定义为有医生诊断报告的病史。17q21 上与 ORMDL3(rs8076131)和 GSDMB(rs7216389,rs2290400)相关的单核苷酸多态性进行了基因分型。
在 17q21 上携带已知哮喘风险等位基因的儿童中,早期喘息与年长兄弟姐妹的存在呈正相关(例如,rs8076131)(调整后的优势比[aOR],1.53;95%置信区间[CI],1.16-2.01)。暴露于农场动物棚与喘息呈负相关(aOR,0.44;95%CI,0.33-0.60)。在没有随后发展为哮喘的 3 岁以下有短暂喘息的儿童中,这两种效应都有类似的观察结果(aOR,1.71[95%CI,1.09-2.67];aOR,0.48[95%CI,0.30-0.76])。
这些发现表明,17 号染色体 q21 位点与短暂喘息和哮喘共有的急性气道阻塞发作有关。先前确定的哮喘风险等位基因易受环境影响。因此,这种基因-环境相互作用揭示了 17q21 的两个方面:相同的基因型构成遗传风险,并允许环境保护,从而为前瞻性预防策略提供了选择。