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交通、哮喘和遗传学:结合国际出生队列数据,研究遗传因素作为交通相关空气污染对儿童哮喘影响的中介。

Traffic, asthma and genetics: combining international birth cohort data to examine genetics as a mediator of traffic-related air pollution's impact on childhood asthma.

机构信息

School of Population and Public Health, University of British Columbia, 2206 East Mall, Vancouver, BC, V6T1Z3, Canada.

出版信息

Eur J Epidemiol. 2013 Jul;28(7):597-606. doi: 10.1007/s10654-013-9828-5. Epub 2013 Jul 24.

DOI:10.1007/s10654-013-9828-5
PMID:23880893
Abstract

Associations between traffic-related air pollution and incident childhood asthma can be strengthened by analysis of gene-environment interactions, but studies have typically been limited by lack of study power. We combined data from six birth cohorts on: asthma, eczema and allergic rhinitis to 7/8 years, and candidate genes. Individual-level assessment of traffic-related air pollution exposure was estimated using land use regression or dispersion modeling. A total of 11,760 children were included in the Traffic, Asthma and Genetics (TAG) Study; 6.3 % reported physician-diagnosed asthma at school-age, 16.0 % had asthma at anytime during childhood, 14.1 % had allergic rhinitis at school-age, 10.0 % had eczema at school-age and 33.1 % were sensitized to any allergen. For GSTP1 rs1138272, the prevalence of heterozygosity was 16 % (range amongst individual cohorts, 11-17 %) and homozygosity for the minor allele was 1 % (0-2 %). For GSTP1 rs1695, the prevalence of heterozygosity was 45 % (40-48 %) and homozygosity for the minor allele, 12 % (10-12 %). For TNF rs1800629, the prevalence of heterozygosity was 29 % (25-32 %) and homozygosity for the minor allele, 3 % (1-3 %). TAG comprises a rich database, the largest of its kind, for investigating the effect of genotype on the association between air pollution and childhood allergic disease.

摘要

交通相关空气污染与儿童哮喘发病的关联可以通过分析基因-环境相互作用得到加强,但此类研究通常因缺乏研究力度而受到限制。我们结合了六个出生队列的数据:7-8 岁时的哮喘、湿疹和过敏性鼻炎,以及候选基因。使用土地利用回归或扩散模型对与交通相关的空气污染暴露进行个体水平评估。共有 11760 名儿童纳入交通、哮喘和遗传学(TAG)研究;6.3%的儿童在学龄期报告有医生诊断的哮喘,16.0%的儿童在整个儿童期都有哮喘,14.1%的儿童在学龄期有过敏性鼻炎,10.0%的儿童在学龄期有湿疹,33.1%的儿童对任何过敏原过敏。对于 GSTP1 rs1138272,杂合性的发生率为 16%(各队列的范围为 11-17%),而次要等位基因的纯合性为 1%(0-2%)。对于 GSTP1 rs1695,杂合性的发生率为 45%(40-48%),而次要等位基因的纯合性为 12%(10-12%)。对于 TNF rs1800629,杂合性的发生率为 29%(25-32%),而次要等位基因的纯合性为 3%(1-3%)。TAG 包含了一个丰富的数据库,是同类研究中最大的数据库,用于研究基因型对空气污染与儿童过敏性疾病之间关联的影响。

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