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BACKGROUND: , have been identified as causal for CAVS. We aimed to identify additional susceptibility genes for CAVS. METHODS: A GWAS (genome-wide association study) meta-analysis of 4 cohorts, totaling 5115 cases and 354 072 controls of European descent, was performed. A TWAS (transcriptome-wide association study) was completed to integrate transcriptomic data from 233 human aortic valves. A series of post-GWAS analyses were performed, including fine-mapping, colocalization, phenome-wide association studies, pathway, and tissue enrichment as well as genetic correlation with cardiovascular traits. RESULTS: lead variant colocalized with higher pulse pressure and higher prevalence of carotid artery stenosis. Association results at the genome-wide scale indicated genetic correlation between CAVS, coronary artery disease, and cardiovascular risk factors. CONCLUSIONS: Our study implicates 3 new genetic loci in CAVS pathogenesis, which constitute novel targets for the development of therapeutic agents.
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Sébastien Thériault
Christian Dina
David Messika‐Zeitoun
Circulation Genomic and Precision Medicine
Centre National de la Recherche Scientifique
Inserm
Université Paris Cité
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Thériault et al. (Tue,) studied this question.
www.synapsesocial.com/papers/69ff780ce4618ba4162d7cba — DOI: https://doi.org/10.1161/circgen.119.002617