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GWAS Study

Genome-wide interaction study of gene-by-occupational exposures on respiratory symptoms.

Zeng X, Vonk JM, van der Plaat DA et al.

30449631 PubMed ID
GWAS Study Type
14765 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

ZX
Zeng X
VJ
Vonk JM
VD
van der Plaat DA
FA
Faiz A
PP
Paré PD
JP
Joubert P
ND
Nickle D
BC
Brandsma CA
KH
Kromhout H
VR
Vermeulen R
XX
Xu X
HX
Huo X
DJ
de Jong K
BH
Boezen HM
Chapter II

Abstract

Summary of the research findings

Respiratory symptoms are important indicators of respiratory diseases. Both genetic and environmental factors contribute to respiratory symptoms development but less is known about gene-environment interactions. We aimed to assess interactions between single nucleotide polymorphisms (SNPs) and occupational exposures on respiratory symptoms cough, dyspnea and phlegm. As identification cohort LifeLines I (n = 7976 subjects) was used. Job-specific exposure was estimated using the ALOHA + job exposure matrix. SNP-by-occupational exposure interactions on respiratory symptoms were tested using logistic regression adjusted for gender, age, and current smoking. SNP-by-exposure interactions with a p-value <10-4 were tested for replication in two independent cohorts: LifeLines II (n = 5260) and the Vlagtwedde-Vlaardingen cohort (n = 1529). The interaction estimates of the replication cohorts were meta-analyzed using PLINK. Replication was achieved when the meta-analysis p-value was <0.05 and the interaction effect had the same direction as in the identification cohort. Additionally, we assessed whether replicated SNPs associated with gene expression by analyzing if they were cis-acting expression quantitative trait loci (eQTL) in lung tissue. In the replication meta-analysis, sixteen out of 477 identified SNP-by-occupational exposure interactions had a p-value <0.05 and 9 of these interactions had the same direction as in the identification cohort. Several identified loci were plausible candidates for respiratory symptoms, such as TMPRSS9, SERPINH1, TOX3, and ARHGAP18. Three replicated SNPs were cis-eQTLs for FCER1A, CHN1, and TIMM13 in lung tissue. Taken together, this genome-wide SNP-by-occupational exposure interaction study in relation to cough, dyspnea, and phlegm identified several suggestive susceptibility genes. Further research should determine if these genes are true susceptibility loci for respiratory symptoms in relation to occupational exposures.

675 Dutch ancestry cough cases, 7,301 Dutch ancestry controls

Chapter III

Study Statistics

Key metrics and study information

14765
Total Participants
GWAS
Study Type
Yes
Replicated
584 Dutch ancestry cough cases, 6,205 Dutch ancestry controls
Replication Participants
European
Ancestry
Netherlands
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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Analysis In Progress

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