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The Association of Novel Single-Nucleotide Variants in the Collagen Matrix-Encoding Gene PRDM5 with Aortic Aneurysmal Disease

Thoracic aortic aneurysms are clinical conditions that are associated with severe clinical endpoints including dissection and rupture, potentially leading to sudden death. Contrary to their abdominal counterparts, thoracic aortic aneurysms are well-recognized to have a genetic basis underlying their...

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Detalles Bibliográficos
Autores principales: Moore, Peyton, Wolf, Adam, Sathyamoorthy, Mohanakrishnan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10455947/
https://www.ncbi.nlm.nih.gov/pubmed/37629506
http://dx.doi.org/10.3390/life13081649
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author Moore, Peyton
Wolf, Adam
Sathyamoorthy, Mohanakrishnan
author_facet Moore, Peyton
Wolf, Adam
Sathyamoorthy, Mohanakrishnan
author_sort Moore, Peyton
collection PubMed
description Thoracic aortic aneurysms are clinical conditions that are associated with severe clinical endpoints including dissection and rupture, potentially leading to sudden death. Contrary to their abdominal counterparts, thoracic aortic aneurysms are well-recognized to have a genetic basis underlying their development. Among all patients with aneurysmal disease who underwent clinical genetic screening in our program (N = 145), two patients were found to have variants of uncertain significance (VUS) in the PRDM5 gene. This gene is responsible for multiple regulatory functions in extracellular matrix development, and this is the first report, to our knowledge, to associate this gene with aortopathy.
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spelling pubmed-104559472023-08-26 The Association of Novel Single-Nucleotide Variants in the Collagen Matrix-Encoding Gene PRDM5 with Aortic Aneurysmal Disease Moore, Peyton Wolf, Adam Sathyamoorthy, Mohanakrishnan Life (Basel) Communication Thoracic aortic aneurysms are clinical conditions that are associated with severe clinical endpoints including dissection and rupture, potentially leading to sudden death. Contrary to their abdominal counterparts, thoracic aortic aneurysms are well-recognized to have a genetic basis underlying their development. Among all patients with aneurysmal disease who underwent clinical genetic screening in our program (N = 145), two patients were found to have variants of uncertain significance (VUS) in the PRDM5 gene. This gene is responsible for multiple regulatory functions in extracellular matrix development, and this is the first report, to our knowledge, to associate this gene with aortopathy. MDPI 2023-07-28 /pmc/articles/PMC10455947/ /pubmed/37629506 http://dx.doi.org/10.3390/life13081649 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Moore, Peyton
Wolf, Adam
Sathyamoorthy, Mohanakrishnan
The Association of Novel Single-Nucleotide Variants in the Collagen Matrix-Encoding Gene PRDM5 with Aortic Aneurysmal Disease
title The Association of Novel Single-Nucleotide Variants in the Collagen Matrix-Encoding Gene PRDM5 with Aortic Aneurysmal Disease
title_full The Association of Novel Single-Nucleotide Variants in the Collagen Matrix-Encoding Gene PRDM5 with Aortic Aneurysmal Disease
title_fullStr The Association of Novel Single-Nucleotide Variants in the Collagen Matrix-Encoding Gene PRDM5 with Aortic Aneurysmal Disease
title_full_unstemmed The Association of Novel Single-Nucleotide Variants in the Collagen Matrix-Encoding Gene PRDM5 with Aortic Aneurysmal Disease
title_short The Association of Novel Single-Nucleotide Variants in the Collagen Matrix-Encoding Gene PRDM5 with Aortic Aneurysmal Disease
title_sort association of novel single-nucleotide variants in the collagen matrix-encoding gene prdm5 with aortic aneurysmal disease
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10455947/
https://www.ncbi.nlm.nih.gov/pubmed/37629506
http://dx.doi.org/10.3390/life13081649
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