基因-空气污染相互作用和遗传样本多样性:南加州儿童健康研究。

IF 1.7 4区 医学 Q3 GENETICS & HEREDITY
Justine Po, John Morrison, Brittney Marian, Zhanghua Chen, W. James Gauderman, Erika Garcia
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引用次数: 0

摘要

已经观察到儿童哮喘的基因-环境相互作用,但很少在不同种族的人群中进行评估。因此,我们研究了多基因风险评分(PRS)如何改变环境空气污染暴露之间的关系(二氧化氮[NO2],臭氧,颗粒物-PRS相互作用在整个样本中具有临界显著性(系数:0.23 [95% CI: -0.03, 0.49])。有限的证据表明,PRS和二氧化氮暴露与哮喘发病率之间存在正相互作用;然而,在西班牙裔参与者中,基于文献的PRS与哮喘无关。公平,多样化的遗传采样方法需要更好地识别临床相关的snp在这一人群。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Gene−Air Pollution Interaction and Diversity of Genetic Sampling: The Southern California Children's Health Study

Gene−environment interactions have been observed for childhood asthma, however few have been assessed in ethnically diverse populations. Thus, we examined how polygenic risk score (PRS) modifies the association between ambient air pollution exposure (nitrogen dioxide [NO2], ozone, particulate matter < 2.5 and < 10 μm) and childhood asthma incidence in a diverse cohort. Participants (n = 1794) were drawn from the Southern California Children's Health Study, a multi-wave prospective cohort followed from 4th to 12th grade. PRS was developed using single nucleotide polymorphisms previously associated with childhood asthma. PRS−asthma associations and PRS−air pollutant interactions were estimated using Poisson regression. An interquartile range PRS increase was associated with 36% (95% CI: 9%, 70%) higher asthma incidence among non-Hispanic children, but not associated with asthma among Hispanic children (rate ratio: 0.81 [95% CI: 0.62, 1.04]). NO2−PRS interaction was borderline significant in the overall sample (coefficient: 0.23 [95% CI: −0.03, 0.49]). Limited evidence was observed for a positive interaction between PRS and NO2 exposure associated with asthma incidence; however, the literature-based PRS was not associated with asthma among Hispanic participants. Equitable, diverse genetic sampling approaches are needed to better identify clinically relevant SNPs in this population.

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来源期刊
Genetic Epidemiology
Genetic Epidemiology 医学-公共卫生、环境卫生与职业卫生
CiteScore
4.40
自引率
9.50%
发文量
49
审稿时长
6-12 weeks
期刊介绍: Genetic Epidemiology is a peer-reviewed journal for discussion of research on the genetic causes of the distribution of human traits in families and populations. Emphasis is placed on the relative contribution of genetic and environmental factors to human disease as revealed by genetic, epidemiological, and biologic investigations. Genetic Epidemiology primarily publishes papers in statistical genetics, a research field that is primarily concerned with development of statistical, bioinformatical, and computational models for analyzing genetic data. Incorporation of underlying biology and population genetics into conceptual models is favored. The Journal seeks original articles comprising either applied research or innovative statistical, mathematical, computational, or genomic methodologies that advance studies in genetic epidemiology. Other types of reports are encouraged, such as letters to the editor, topic reviews, and perspectives from other fields of research that will likely enrich the field of genetic epidemiology.
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