4.6 Article

Interaction between Genetic Risk Scores for reduced pulmonary function and smoking, asthma and endotoxin

Journal

THORAX
Volume 76, Issue 12, Pages 1219-1226

Publisher

BMJ PUBLISHING GROUP
DOI: 10.1136/thoraxjnl-2020-215624

Keywords

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Funding

  1. Intramural Research Programme of the National Institutes of Health, National Institute of Environmental Health Sciences [Z01-ES102385, Z01-ES049030, Z01-ES043012, HHSN273201600003I]
  2. National Cancer Institute [Z01-CP010119]
  3. American Recovery and Reinvestment Act funds through National Institute of Environmental Health Sciences [N01- ES-55546]
  4. [PHR-SUPS2-S-10-00179]
  5. [NIH P30 ES005605]

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This study evaluated the impact of gene-environment interactions on pulmonary function using Genetic Risk Scores (GRSs). The results suggest that increased genetic susceptibility has a greater impact on reduced pulmonary function in the presence of smoking or asthma.
Rationale Genome-wide association studies (GWASs) have identified numerous lod associated with lower pulmonary function. Pulmonary function is strongly related to smoking and has also been associated with asthma and dust endotoxin. At the individual SNP level genome-wide analyses of pulmonary function have not identified appreciable evidence for gene by environment interactions. Genetic Risk Scores (GRSs) may enhance power to identify gene-environment interactions, but studies are few. Methods We analysed 2844 individuals of European ancestry with 1000 Genomes imputed GWAS data from a case-control study of adult asthma nested within a US agricultural cohort. Pulmonary function traits were FEV1/FVC and FEV1/FVC. Using data from a recent large meta-analysis of GWAS, we constructed a weighted GRS for each trait by combining the top (p value<5x10(-9)) genetic variants, after clumping based on distance (+/- 250 kb) and linkage disequilibrium (r(2)=0.5).We used linear regression, adjusting for relevant covariates, to estimate associations of each trait with its GRS and to assess interactions. Results Each trait was highly significanty associated with its GRS (all three p values<8.9x10(-8)). The inverse association of the GRS with FEV,/FVC was stronger for current smokers (p(interaction)=0.017) or former smokers (p(interaction)=0.064) when compared with never smokers and among asthmatics compared with non-asthmatics (p(interaction)=0.053). No significant interactions were observed between any GRS and house dust endotoxin. Conclusions Evaluation of interactions using GRSs supports a greater impact of increased genetic susceptibility on reduced pulmonary function in the presence of smoking or asthma.

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