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Effect of 6p21 region on lung function is modified by smoking: a genome-wide interaction study
Smoking is a major risk factor for chronic obstructive pulmonary disease (COPD); however, more than 25% of COPD patients are non-smokers, and gene-by-smoking interactions are expected to affect COPD onset. We aimed to identify the common genetic variants interacting with pack-years of smoking on FEV...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7403370/ https://www.ncbi.nlm.nih.gov/pubmed/32753590 http://dx.doi.org/10.1038/s41598-020-70092-0 |
Sumario: | Smoking is a major risk factor for chronic obstructive pulmonary disease (COPD); however, more than 25% of COPD patients are non-smokers, and gene-by-smoking interactions are expected to affect COPD onset. We aimed to identify the common genetic variants interacting with pack-years of smoking on FEV(1)/FVC ratios in individuals with normal lung function. A genome-wide interaction study (GWIS) on FEV(1)/FVC was performed for individuals with FEV(1)/FVC ratio ≥ 70 in the Korea Associated Resource cohort data, and significant SNPs were validated using data from two other Korean cohorts. The GWIS revealed that rs10947231 and rs8192575 met genome-wide significant levels; For [Formula: see text] the likelihood ratio (LR) test was conducted, and its P values, P(LR), for rs10947231 and rs8192575 were 2.23 × 10(–12) and 1.18 × 10(–8), respectively. Interaction between rs8192575 and smoking is significantly replicated with two additional data (P(INT) = 0.0454, 0.0131). Expression quantitative trait loci, topologically associated domains, and PrediXcan analyses revealed that rs8192575 is significantly associated with AGER expression. SNPs on the 6p21 region are associated with FEV(1)/FVC, and the effect of smoking on FEV(1)/FVC differs among the associated genotypes. |
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