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

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 =...

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Autores principales: Thériault, Sébastien, Gaudreault, Nathalie, Lamontagne, Maxime, Rosa, Mickael, Boulanger, Marie-Chloé, Messika-Zeitoun, David, Clavel, Marie-Annick, Capoulade, Romain, Dagenais, François, Pibarot, Philippe, Mathieu, Patrick, Bossé, Yohan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5840407/
https://www.ncbi.nlm.nih.gov/pubmed/29511167
http://dx.doi.org/10.1038/s41467-018-03260-6
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author Thériault, Sébastien
Gaudreault, Nathalie
Lamontagne, Maxime
Rosa, Mickael
Boulanger, Marie-Chloé
Messika-Zeitoun, David
Clavel, Marie-Annick
Capoulade, Romain
Dagenais, François
Pibarot, Philippe
Mathieu, Patrick
Bossé, Yohan
author_facet Thériault, Sébastien
Gaudreault, Nathalie
Lamontagne, Maxime
Rosa, Mickael
Boulanger, Marie-Chloé
Messika-Zeitoun, David
Clavel, Marie-Annick
Capoulade, Romain
Dagenais, François
Pibarot, Philippe
Mathieu, Patrick
Bossé, Yohan
author_sort Thériault, Sébastien
collection PubMed
description 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.
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spelling pubmed-58404072018-03-09 A transcriptome-wide association study identifies PALMD as a susceptibility gene for calcific aortic valve stenosis Thériault, Sébastien Gaudreault, Nathalie Lamontagne, Maxime Rosa, Mickael Boulanger, Marie-Chloé Messika-Zeitoun, David Clavel, Marie-Annick Capoulade, Romain Dagenais, François Pibarot, Philippe Mathieu, Patrick Bossé, Yohan Nat Commun Article 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. Nature Publishing Group UK 2018-03-07 /pmc/articles/PMC5840407/ /pubmed/29511167 http://dx.doi.org/10.1038/s41467-018-03260-6 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Thériault, Sébastien
Gaudreault, Nathalie
Lamontagne, Maxime
Rosa, Mickael
Boulanger, Marie-Chloé
Messika-Zeitoun, David
Clavel, Marie-Annick
Capoulade, Romain
Dagenais, François
Pibarot, Philippe
Mathieu, Patrick
Bossé, Yohan
A transcriptome-wide association study identifies PALMD as a susceptibility gene for calcific aortic valve stenosis
title A transcriptome-wide association study identifies PALMD as a susceptibility gene for calcific aortic valve stenosis
title_full A transcriptome-wide association study identifies PALMD as a susceptibility gene for calcific aortic valve stenosis
title_fullStr A transcriptome-wide association study identifies PALMD as a susceptibility gene for calcific aortic valve stenosis
title_full_unstemmed A transcriptome-wide association study identifies PALMD as a susceptibility gene for calcific aortic valve stenosis
title_short A transcriptome-wide association study identifies PALMD as a susceptibility gene for calcific aortic valve stenosis
title_sort transcriptome-wide association study identifies palmd as a susceptibility gene for calcific aortic valve stenosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5840407/
https://www.ncbi.nlm.nih.gov/pubmed/29511167
http://dx.doi.org/10.1038/s41467-018-03260-6
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