Genetic overlap of chronic obstructive pulmonary disease and cardiovascular disease-related traits: a large-scale genome-wide cross-trait analysis
Year: 2019
Type: article
Study design: Observational Study
Abstract: A growing number of studies clearly demonstrate a substantial association between chronic obstructive pulmonary disease (COPD) and cardiovascular diseases (CVD), although little is known about the shared genetics that contribute to this association. We conducted a large-scale cross-trait genome-wide association study to investigate genetic overlap between COPD (N case = 12,550, N control = 46,368) from the International COPD Genetics Consortium and four primary cardiac traits: resting heart rate (RHR) ( N = 458,969), high blood pressure (HBP) (N case = 144,793, N control = 313,761), coronary artery disease (CAD)(N case = 60,801, N control = 123,504), and stroke (N case = 40,585, N control = 406,111) from UK Biobank, CARDIoGRAMplusC4D Consortium, and International Stroke Genetics Consortium data. RHR and HBP had modest genetic correlation, and CAD had borderline evidence with COPD at a genome-wide level. We found evidence of local genetic correlation with particular regions of the genome. Cross-trait meta-analysis of COPD identified 21 loci jointly associated with RHR, 22 loci with HBP, and 3 loci with CAD. Functional analysis revealed that shared genes were enriched in smoking-related pathways and in cardiovascular, nervous, and immune system tissues. An examination of smoking-related genetic variants identified SNPs located in 15q25.1 region associated with cigarettes per day, with effects on RHR and CAD. A Mendelian randomization analysis showed a significant positive causal effect of COPD on RHR (causal estimate = 0.1374, P = 0.008). In a set of large-scale GWAS, we identify evidence of shared genetics between COPD and cardiac traits.
Source: Respiratory Research
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $2,570
Awards: Identifying Genetic Determinants of Severe, Early-Onset COPD, Identifying functional variants in COPD GWAS loci, Harvard Chan School NIEHS Center for Environmental Health, Multi-omic Subtyping of Chronic Obstructive Pulmonary Disease, Molecular Epidemiology of ARDS, Whole Blood MicroRNAs as Risk and Survival Biomarkers for ARDS, Genetic and Genomic Characterization of the Occurrence and Progression of Interstitial Lung Abnormalities
OpenAlex ID: W2943360370
