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GSTP1 and TNF Gene Variants and Associations between Air Pollution and Incident Childhood Asthma: The Traffic Asthma and Genetics (TAG) Study

机译:GSTP1和TNF基因变异及空气污染与儿童哮喘的关联:交通哮喘和遗传学(TAG)研究

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摘要

Background: Genetics may partially explain observed heterogeneity in associations between traffic-related air pollution and incident asthma.Objective: Our aim was to investigate the impact of gene variants associated with oxidative stress and inflammation on associations between air pollution and incident childhood asthma.Methods: Traffic-related air pollution, asthma, wheeze, gene variant, and potential confounder data were pooled across six birth cohorts. Parents reported physician-diagnosed asthma and wheeze from birth to 7–8 years of age (confirmed by pediatric allergist in two cohorts). Individual estimates of annual average air pollution [nitrogen dioxide (NO2), particulate matter ≤ 2.5 μm (PM2.5), PM2.5 absorbance, ozone] were assigned to each child’s birth address using land use regression, atmospheric modeling, and ambient monitoring data. Effect modification by variants in GSTP1 (rs1138272/Ala114Val and rs1695/IIe105Val) and TNF (rs1800629/G-308A) was investigated.Results: Data on asthma, wheeze, potential confounders, at least one SNP of interest, and NO2 were available for 5,115 children. GSTP1 rs1138272 and TNF rs1800629 SNPs were associated with asthma and wheeze, respectively. In relation to air pollution exposure, children with one or more GSTP1 rs1138272 minor allele were at increased risk of current asthma [odds ratio (OR) = 2.59; 95% CI: 1.43, 4.68 per 10 μg/m3 NO2] and ever asthma (OR = 1.64; 95% CI: 1.06, 2.53) compared with homozygous major allele carriers (OR = 0.95; 95% CI: 0.68, 1.32 for current and OR = 1.20; 95% CI: 0.98, 1.48 for ever asthma; Bonferroni-corrected interaction p = 0.04 and 0.01, respectively). Similarly, for GSTP1 rs1695, associations between NO2 and current and ever asthma had ORs of 1.43 (95% CI: 1.03, 1.98) and 1.36 (95% CI: 1.08, 1.70), respectively, for minor allele carriers compared with ORs of 0.82 (95% CI: 0.52, 1.32) and 1.12 (95% CI: 0.84, 1.49) for homozygous major allele carriers (Bonferroni-corrected interaction p-values 0.48 and 0.09). There were no clear differences by TNF genotype.Conclusions: Children carrying GSTP1 rs1138272 or rs1695 minor alleles may constitute a susceptible population at increased risk of asthma associated with air pollution.Citation: MacIntyre EA, Brauer M, Melén E, Bauer CP, Bauer M, Berdel D, Bergström A, Brunekreef B, Chan-Yeung M, Klümper C, Fuertes E, Gehring U, Gref A, Heinrich J, Herbarth O, Kerkhof M, Koppelman GH, Kozyrskyj AL, Pershagen G, Postma DS, Thiering E, Tiesler CM, Carlsten C, TAG Study Group. 2014. GSTP1 and TNF gene variants and associations between air pollution and incident childhood asthma: the traffic, asthma and genetics (TAG) Study. Environ Health Perspect 122:418–424; 
机译:背景:遗传学可以部分解释在交通相关的空气污染与突发性哮喘之间存在的异质性目的:我们的目的是研究与氧化应激和炎症相关的基因变异对空气污染与儿童突发性哮喘之间关联的影响。与交通相关的空气污染,哮喘,喘息,基因变异和潜在的混杂因素数据汇总在六个出生队列中。父母报告说,从出生到7-8岁,医生诊断为哮喘和喘鸣(由两个小组的儿科过敏症专家确认)。使用土地利用回归,大气模型和环境监测,将每个年度的平均空气污染[二氧化氮(NO2),≤2.5μm的颗粒物(PM2.5),PM2.5的吸收度,臭氧]的单独估算分配给每个孩子的出生地址。数据。研究了GSTP1(rs1138272 / Ala 114 Val和rs1695 / IIe 105 Val)和TNF(rs1800629 / G-308A)的变体对效应的影响。结果:哮喘数据,喘息,潜在的混杂因素,至少一种感兴趣的SNP和NO2可用于5,115名儿童。 GSTP1 rs1138272和TNF rs1800629 SNP分别与哮喘和喘息相关。关于空气污染暴露,患有一个或多个GSTP1 rs1138272次要等位基因的儿童患哮喘的风险增加[比值比(OR)= 2.59;相较于纯合主要等位基因携带者(OR = 0.95; 95),95%CI:每10μg/ m 3 NO2的1.43,4.68]和曾经患过哮喘(OR = 1.64; 95%CI:1.06,2.53) %CI:当前电流的0.68、1.32和OR = 1.20; 95%CI:曾经的哮喘的0.98、1.48;经Bonferroni校正的相互作用p分别为0.04和0.01)。同样,对于GSTP1 rs1695,未成年人等位基因携带者的NO2与当前哮喘和以往哮喘之间的OR分别为1.43(95%CI:1.03,1.98)和1.36(95%CI:1.08,1.70),而ORs为0.82。 (95%CI:0.52,1.32)和1.12(95%CI:0.84,1.49)对于纯合等位基因主要等位基因携带者(Bonferroni校正的相互作用p值0.48和0.09)。结论:携带GSTP1 rs1138272或rs1695小等位基因的儿童可能构成易感人群,罹患与空气污染有关的哮喘的风险增加。引用:MacIntyre EA,Brauer M,MelénE,Bauer CP,Bauer M ,Berdel D,BergströmA,Brunekreef B,Chan-Yeung M,KlümperC,Fuertes E,Gehring U,Gref A,Heinrich J,Herbarth O,Kerkhof M,Koppelman GH,Kozyrskyj AL,Pershagen G,Postma DS,Thiering E ,Tiesler CM,Carlsten C,TAG研究小组。 2014。GSTP1和TNF基因变异以及空气污染与儿童哮喘的关联:交通,哮喘和遗传学(TAG)研究。环境健康观察122:418–424;

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