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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 =...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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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. |
format | Online Article Text |
id | pubmed-5840407 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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