Genetic Insights into Bicuspid Aortic Valve Formation

Bicuspid aortic valve (BAV) is the most common congenital heart defect, affecting 1-2% of the population. It is generally diagnosed late in adulthood when deterioration of the abnormal leaflet becomes clinically evident. BAV patients have an increased risk of developing serious complications, includ...

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Main Authors: Brigitte Laforest, Mona Nemer
Format: Article
Language:English
Published: Wiley 2012-01-01
Series:Cardiology Research and Practice
Online Access:http://dx.doi.org/10.1155/2012/180297
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author Brigitte Laforest
Mona Nemer
author_facet Brigitte Laforest
Mona Nemer
author_sort Brigitte Laforest
collection DOAJ
description Bicuspid aortic valve (BAV) is the most common congenital heart defect, affecting 1-2% of the population. It is generally diagnosed late in adulthood when deterioration of the abnormal leaflet becomes clinically evident. BAV patients have an increased risk of developing serious complications, including stenosis, regurgitation, endocarditis, dilation of the aorta, aortic dissection, and aneurysm. BAV is a heritable trait, but the genetic basis underlying this cardiac malformation remains poorly understood. In the last decade, thanks to studies in animal models as well as genetic and biochemical approaches, a large number of genes that play important roles in heart development have been identified. These discoveries provided valuable insight into cardiac morphogenesis and uncovered congenital-heart-disease-causing genes. This paper will summarize the current knowledge of valve morphogenesis as well as our current understanding of the genetic pathways involved in BAV formation. The impact of these advances on human health including diagnosis of BAV and prevention of cardiovascular complications in individuals with BAV or with a family history of BAV is also discussed.
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spelling doaj-art-77b21b39f209430ba95455bcafdc26ea2025-02-03T05:53:23ZengWileyCardiology Research and Practice2090-80162090-05972012-01-01201210.1155/2012/180297180297Genetic Insights into Bicuspid Aortic Valve FormationBrigitte Laforest0Mona Nemer1Department of Biochemistry, Microbiology and Immunology, University of Ottawa, Ottawa, ON, K1N 6N5, CanadaDepartment of Biochemistry, Microbiology and Immunology, University of Ottawa, Ottawa, ON, K1N 6N5, CanadaBicuspid aortic valve (BAV) is the most common congenital heart defect, affecting 1-2% of the population. It is generally diagnosed late in adulthood when deterioration of the abnormal leaflet becomes clinically evident. BAV patients have an increased risk of developing serious complications, including stenosis, regurgitation, endocarditis, dilation of the aorta, aortic dissection, and aneurysm. BAV is a heritable trait, but the genetic basis underlying this cardiac malformation remains poorly understood. In the last decade, thanks to studies in animal models as well as genetic and biochemical approaches, a large number of genes that play important roles in heart development have been identified. These discoveries provided valuable insight into cardiac morphogenesis and uncovered congenital-heart-disease-causing genes. This paper will summarize the current knowledge of valve morphogenesis as well as our current understanding of the genetic pathways involved in BAV formation. The impact of these advances on human health including diagnosis of BAV and prevention of cardiovascular complications in individuals with BAV or with a family history of BAV is also discussed.http://dx.doi.org/10.1155/2012/180297
spellingShingle Brigitte Laforest
Mona Nemer
Genetic Insights into Bicuspid Aortic Valve Formation
Cardiology Research and Practice
title Genetic Insights into Bicuspid Aortic Valve Formation
title_full Genetic Insights into Bicuspid Aortic Valve Formation
title_fullStr Genetic Insights into Bicuspid Aortic Valve Formation
title_full_unstemmed Genetic Insights into Bicuspid Aortic Valve Formation
title_short Genetic Insights into Bicuspid Aortic Valve Formation
title_sort genetic insights into bicuspid aortic valve formation
url http://dx.doi.org/10.1155/2012/180297
work_keys_str_mv AT brigittelaforest geneticinsightsintobicuspidaorticvalveformation
AT monanemer geneticinsightsintobicuspidaorticvalveformation