Back to Search Start Over

Genetic association analyses highlight IL6, ALPL, and NAV1 as three new susceptibility genes underlying calcific aortic valve stenosis

Authors :
Nathalie Gaudreault
Richard Redon
Jean-Jacques Schott
Solena Le Scouarnec
Patrick Mathieu
Yohan Bossé
Christian Dina
Simon Lecointe
Thierry Le Tourneau
Stéphanie Bonnaud
Jean Philippe Verhoye
Philippe Pibarot
Zhonglin Li
Eric Charpentier
Anne-Sophie Boureau
Sidwell Rigade
Floriane Simonet
Sébastien Thériault
Christophe Baufreton
Romain Capoulade
Ronan Roussel
Estelle Baron
François Dagenais
Matilde Karakachoff
Maxime Lamontagne
Imen Fellah
Vincent Probst
Marie-Annick Clavel
David Messika-Zeitoun
Benoit J. Arsenault
Jean-Christian Roussel
Publication Year :
2019
Publisher :
Cold Spring Harbor Laboratory, 2019.

Abstract

To date, only two replicated loci, LPA and PALMD, have been identified as causal genes for calcific aortic valve stenosis (CAVS) using genome-wide and transcriptome-wide association study (TWAS). To identify additional susceptibility genes for CAVS, we performed a GWAS meta-analysis totaling 5,115 cases and 354,072 controls of European descent. Four loci achieved genome-wide significance, including two new loci: IL6 (interleukin 6) on 7p15.3 and ALPL (alkaline phosphatase) on 1p36.12. A TWAS integrating an eQTL study of 233 human aortic valves identified NAV1 (neuron navigator 1) on 1q32.1 as a new candidate causal gene. The CAVS risk alleles were associated with higher mRNA expression of NAV1 in valve tissues. Association results at the genome-wide scale showed genetic correlation with coronary artery disease and cardiovascular risk factors. Our study highlights three new loci implicating inflammation, mineralization and blood vessel integrity in CAVS pathogenesis and supports shared genetic etiology with cardiovascular traits.

Details

Database :
OpenAIRE
Accession number :
edsair.doi.dedup.....884421bc03bad38ebdf491779fc10dfb