Menu
Currency
GWAS Study

A transcriptome-wide association study identifies PALMD as a susceptibility gene for calcific aortic valve stenosis.

Thériault S, Gaudreault N, Lamontagne M et al.

29511167 PubMed ID
GWAS Study Type
355612 Participants
141 Views
Scroll to explore
Chapter I

Publication Details

Comprehensive information about this research publication

Authors

TS
Thériault S
GN
Gaudreault N
LM
Lamontagne M
RM
Rosa M
BM
Boulanger MC
MD
Messika-Zeitoun D
CM
Clavel MA
CR
Capoulade R
DF
Dagenais F
PP
Pibarot P
MP
Mathieu P
BY
Bossé Y
Chapter II

Abstract

Summary of the research findings

Calcific aortic valve stenosis (CAVS) is a common and life-threatening heart disease and the current treatment options cannot stop or delay its progression. A GWAS on 1009 cases and 1017 ethnically matched controls was combined with a large-scale eQTL mapping study of human aortic valve tissues (n = 233) to identify susceptibility genes for CAVS. Replication was performed in the UK Biobank, including 1391 cases and 352,195 controls. A transcriptome-wide association study (TWAS) reveals PALMD (palmdelphin) as significantly associated with CAVS. The CAVS risk alleles and increasing disease severity are both associated with decreased mRNA expression levels of PALMD in valve tissues. The top variant identified shows a similar effect and strong association with CAVS (P = 1.53 × 10-10) in UK Biobank. The identification of PALMD as a susceptibility gene for CAVS provides insights into the genetic nature of this disease, opens avenues to investigate its etiology and to develop much-needed therapeutic options.

1,009 French Canadian cases, 1,017 French Canadian controls

Chapter III

Study Statistics

Key metrics and study information

355612
Total Participants
GWAS
Study Type
Yes
Replicated
1,391 European ancestry cases, 352,195 European ancestry controls
Replication Participants
European
Ancestry
U.K., Canada
Recruitment Country
Chapter IV

AI-Generated Summary

AI-generated by DNAGENICS

Independent AI summary of health and genetic findings from the published study

Important: This summary is AI-generated by DNAGENICS for informational purposes only. It was not created by, affiliated with, or endorsed by the researchers behind the original publication, and is based solely on that published research. It may contain errors or omissions. DNAGENICS disclaims all liability for any inaccuracies or consequences arising from use of this information. Verify all information against the original publication. This is not professional scientific review or medical advice.

AI Summary In Progress

Our AI-generated summary of this publication is being prepared. Please check back soon.