Modeling Unobserved Heterogeneity in Susceptibility to Ambient Benzo[a]pyrene Concentration among Children with Allergic Asthma Using an Unsupervised Learning Algorithm
Jazyk angličtina Země Švýcarsko Médium electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
29320438
PubMed Central
PMC5800205
DOI
10.3390/ijerph15010106
PII: ijerph15010106
Knihovny.cz E-zdroje
- Klíčová slova
- air pollution, asthma, gene-environment interaction, polycyclic aromatic hydrocarbon, single nucleotide polymorphism,
- MeSH
- algoritmy MeSH
- benzopyren toxicita MeSH
- bronchiální astma chemicky indukované genetika MeSH
- dítě MeSH
- genetická predispozice k nemoci * MeSH
- interakce genů a prostředí MeSH
- jednonukleotidový polymorfismus MeSH
- látky znečišťující vzduch toxicita MeSH
- lidé MeSH
- multifaktoriální dědičnost * MeSH
- statistika jako téma MeSH
- strojové učení bez učitele MeSH
- studie případů a kontrol MeSH
- vystavení vlivu životního prostředí škodlivé účinky MeSH
- znečištění ovzduší škodlivé účinky MeSH
- Check Tag
- dítě MeSH
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- benzopyren MeSH
- látky znečišťující vzduch MeSH
Current studies of gene × air pollution interaction typically seek to identify unknown heritability of common complex illnesses arising from variability in the host's susceptibility to environmental pollutants of interest. Accordingly, a single component generalized linear models are often used to model the risk posed by an environmental exposure variable of interest in relation to a priori determined DNA variants. However, reducing the phenotypic heterogeneity may further optimize such approach, primarily represented by the modeled DNA variants. Here, we reduce phenotypic heterogeneity of asthma severity, and also identify single nucleotide polymorphisms (SNP) associated with phenotype subgroups. Specifically, we first apply an unsupervised learning algorithm method and a non-parametric regression to find a biclustering structure of children according to their allergy and asthma severity. We then identify a set of SNPs most closely correlated with each sub-group. We subsequently fit a logistic regression model for each group against the healthy controls using benzo[a]pyrene (B[a]P) as a representative airborne carcinogen. Application of such approach in a case-control data set shows that SNP clustering may help to partly explain heterogeneity in children's asthma susceptibility in relation to ambient B[a]P concentration with greater efficiency.
Genedata AG Margarethenstrasse 38 CH 4053 Basel Switzerland
School of Mathematics and Statistics Victoria University of Wellington Wellington 6140 New Zealand
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Airborne Benzo[a]Pyrene may contribute to divergent Pheno-Endotypes in children