Improved Annotation of Asthma Gene Variants with Cell Type Deconvolution of Nasal and Lung Expression-Quantitative Trait Loci.

Asthma is a genetically complex inflammatory airway disease associated with over 200 Single nucleotide polymorphisms (SNPs). However, the functional effects of many asthma-associated SNPs in lung and airway epithelial samples are unknown. Here, we aimed to conduct expression quantitative trait loci (eQTL) analysis using a meta-analysis of nasal and lung samples. We hypothesize that incorporating cell-type proportions of airway and lung samples enhances eQTL analysis outcomes. Nasal brush (n=792) and lung tissue (n=1087) samples were investigated separately. Initially, a general eQTL analysis identified genetic variants associated with gene expression levels. Estimated cell-type proportions were adjusted based on the Human Lung Cell Atlas. Additionally, the presence of significant interaction effects between asthma-associated SNPs and each cell type proportion was explored and considered evidence for cell-type associated eQTL. In nasal brush and lung parenchyma samples, 44 and 116 asthma-associated SNPs were identified as eQTLs. Adjusting for cell-type proportions revealed eQTLs for an additional 17 genes (e.g., FCER1G, CD200R1, and GABBR2) and 16 Genes (e.g., CYP2C8, SLC9A2, and SGCD) in nose and lung, respectively. Moreover, we identified eQTLs for 9 SNPs annotated to genes such as VASP, FOXA3, PCDHB12 displayed significant interactions with cell type proportions of Club, Goblet, and alveolar macrophages. Our findings demonstrate increased power for identifying eQTLs among asthma-associated SNPs by considering cell-type proportion of the bulk-RNA-seq data from nasal and lung tissues. Integration of cell-type deconvolution and eQTL analysis enhances our understanding of asthma genetics and cellular mechanisms, uncovering potential therapeutic targets for personalized interventions.