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HAS-1 genetic polymorphism in sporadic abdominal aortic aneurysm

The hyaluronan synthase 1 (HAS-1) gene encodes a plasma membrane protein that synthesizes hyaluronan (HA), an extracellular matrix molecule. Accumulating evidence emphasizes the relevance of HA metabolism in an increasing number of processes of clinical interest, including abdominal aortic aneurysm...

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Autores principales: Armani, Chiara, Landi, Stefano, Nuti, Marco, Di Stefano, Rossella, Balbarini, Alberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Publications 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3184700/
https://www.ncbi.nlm.nih.gov/pubmed/21977277
http://dx.doi.org/10.4081/hi.2009.e1
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author Armani, Chiara
Landi, Stefano
Nuti, Marco
Di Stefano, Rossella
Balbarini, Alberto
author_facet Armani, Chiara
Landi, Stefano
Nuti, Marco
Di Stefano, Rossella
Balbarini, Alberto
author_sort Armani, Chiara
collection PubMed
description The hyaluronan synthase 1 (HAS-1) gene encodes a plasma membrane protein that synthesizes hyaluronan (HA), an extracellular matrix molecule. Accumulating evidence emphasizes the relevance of HA metabolism in an increasing number of processes of clinical interest, including abdominal aortic aneurysm (AAA). The existence of aberrant splicing variants of the HAS-1 gene could partly explain the altered extracellular matrix architecture and influence various biological functions, resulting in progressive arterial wall failure in the development of AAA. In the present study, we assessed the hypothesis that HAS-1 genetic 833A/G polymorphism could be associated with the risk of AAA by performing a case-control association study, involving AAA patients and healthy matched donors.
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spelling pubmed-31847002011-10-05 HAS-1 genetic polymorphism in sporadic abdominal aortic aneurysm Armani, Chiara Landi, Stefano Nuti, Marco Di Stefano, Rossella Balbarini, Alberto Heart Int Article The hyaluronan synthase 1 (HAS-1) gene encodes a plasma membrane protein that synthesizes hyaluronan (HA), an extracellular matrix molecule. Accumulating evidence emphasizes the relevance of HA metabolism in an increasing number of processes of clinical interest, including abdominal aortic aneurysm (AAA). The existence of aberrant splicing variants of the HAS-1 gene could partly explain the altered extracellular matrix architecture and influence various biological functions, resulting in progressive arterial wall failure in the development of AAA. In the present study, we assessed the hypothesis that HAS-1 genetic 833A/G polymorphism could be associated with the risk of AAA by performing a case-control association study, involving AAA patients and healthy matched donors. PAGEPress Publications 2009-06-30 /pmc/articles/PMC3184700/ /pubmed/21977277 http://dx.doi.org/10.4081/hi.2009.e1 Text en ©Copyright Chiara Armani et al., 2009 This work is licensed under a Creative Commons Attribution 3.0 License (by-nc 3.0). Licensee PAGEPress, Italy
spellingShingle Article
Armani, Chiara
Landi, Stefano
Nuti, Marco
Di Stefano, Rossella
Balbarini, Alberto
HAS-1 genetic polymorphism in sporadic abdominal aortic aneurysm
title HAS-1 genetic polymorphism in sporadic abdominal aortic aneurysm
title_full HAS-1 genetic polymorphism in sporadic abdominal aortic aneurysm
title_fullStr HAS-1 genetic polymorphism in sporadic abdominal aortic aneurysm
title_full_unstemmed HAS-1 genetic polymorphism in sporadic abdominal aortic aneurysm
title_short HAS-1 genetic polymorphism in sporadic abdominal aortic aneurysm
title_sort has-1 genetic polymorphism in sporadic abdominal aortic aneurysm
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3184700/
https://www.ncbi.nlm.nih.gov/pubmed/21977277
http://dx.doi.org/10.4081/hi.2009.e1
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