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Aorta Measurements are Heritable and Influenced by Bicuspid Aortic Valve

Objectives: To determine whether the contributions of genetics and bicuspid aortic valve (BAV) independently influence aortic (Ao) dimensions. Background: Ao dilation is a risk factor for aneurysm, dissection, and sudden cardiac death. Frequent association of BAV with Ao dilation implicates a common...

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Autores principales: Martin, Lisa J., Hinton, Robert B., Zhang, Xue, Cripe, Linda H., Benson, D. Woodrow
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3268614/
https://www.ncbi.nlm.nih.gov/pubmed/22303356
http://dx.doi.org/10.3389/fgene.2011.00061
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author Martin, Lisa J.
Hinton, Robert B.
Zhang, Xue
Cripe, Linda H.
Benson, D. Woodrow
author_facet Martin, Lisa J.
Hinton, Robert B.
Zhang, Xue
Cripe, Linda H.
Benson, D. Woodrow
author_sort Martin, Lisa J.
collection PubMed
description Objectives: To determine whether the contributions of genetics and bicuspid aortic valve (BAV) independently influence aortic (Ao) dimensions. Background: Ao dilation is a risk factor for aneurysm, dissection, and sudden cardiac death. Frequent association of BAV with Ao dilation implicates a common underlying defect possibly due to genetic factors. Methods: Families enriched for BAV underwent standardized transthoracic echocardiography. In addition to BAV status, echocardiographic measures of Ao (annulus to descending Ao), pulmonary artery, and mitral valve annulus (MVA) diameters were obtained. Using variance components analysis, heritability was estimated with and without BAV status. Additionally, bivariate genetic analyses between Ao dimensions and BAV were performed. Results: Our cohort was obtained from 209 families enriched for BAV. After adjusting for age, body surface area, and sex, individuals with BAV had a statistically significant increase in all echocardiographic measurements (p < 0.006) except descending Ao and MVA. Individuals with BAV were at greater odds of having Ao dilation (OR = 4.44, 95% CI 2.93–6.72) than family members without BAV. All echocardiographic measurements exhibited moderate to strong heritability (0.25–0.53), and these estimates were not influenced by inclusion of BAV as a covariate. Bivariate genetic analyses supported that the genetic correlation between BAV and echo measures were not significantly different from zero. Conclusion: We show for the first time that echocardiographic measurements of Ao, pulmonary artery and MVA diameters are quantitative traits that exhibit significant heritability. In addition, our results suggest the presence of BAV independently influences the proximal Ao and pulmonary artery measures but not those in the descending Ao or MVA.
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spelling pubmed-32686142012-02-02 Aorta Measurements are Heritable and Influenced by Bicuspid Aortic Valve Martin, Lisa J. Hinton, Robert B. Zhang, Xue Cripe, Linda H. Benson, D. Woodrow Front Genet Genetics Objectives: To determine whether the contributions of genetics and bicuspid aortic valve (BAV) independently influence aortic (Ao) dimensions. Background: Ao dilation is a risk factor for aneurysm, dissection, and sudden cardiac death. Frequent association of BAV with Ao dilation implicates a common underlying defect possibly due to genetic factors. Methods: Families enriched for BAV underwent standardized transthoracic echocardiography. In addition to BAV status, echocardiographic measures of Ao (annulus to descending Ao), pulmonary artery, and mitral valve annulus (MVA) diameters were obtained. Using variance components analysis, heritability was estimated with and without BAV status. Additionally, bivariate genetic analyses between Ao dimensions and BAV were performed. Results: Our cohort was obtained from 209 families enriched for BAV. After adjusting for age, body surface area, and sex, individuals with BAV had a statistically significant increase in all echocardiographic measurements (p < 0.006) except descending Ao and MVA. Individuals with BAV were at greater odds of having Ao dilation (OR = 4.44, 95% CI 2.93–6.72) than family members without BAV. All echocardiographic measurements exhibited moderate to strong heritability (0.25–0.53), and these estimates were not influenced by inclusion of BAV as a covariate. Bivariate genetic analyses supported that the genetic correlation between BAV and echo measures were not significantly different from zero. Conclusion: We show for the first time that echocardiographic measurements of Ao, pulmonary artery and MVA diameters are quantitative traits that exhibit significant heritability. In addition, our results suggest the presence of BAV independently influences the proximal Ao and pulmonary artery measures but not those in the descending Ao or MVA. Frontiers Research Foundation 2011-09-05 /pmc/articles/PMC3268614/ /pubmed/22303356 http://dx.doi.org/10.3389/fgene.2011.00061 Text en Copyright © 2011 Martin, Hinton, Zhang, Cripe and Benson. http://www.frontiersin.org/licenseagreement This is an open-access article subject to a non-exclusive license between the authors and Frontiers Media SA, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and other Frontiers conditions are complied with.
spellingShingle Genetics
Martin, Lisa J.
Hinton, Robert B.
Zhang, Xue
Cripe, Linda H.
Benson, D. Woodrow
Aorta Measurements are Heritable and Influenced by Bicuspid Aortic Valve
title Aorta Measurements are Heritable and Influenced by Bicuspid Aortic Valve
title_full Aorta Measurements are Heritable and Influenced by Bicuspid Aortic Valve
title_fullStr Aorta Measurements are Heritable and Influenced by Bicuspid Aortic Valve
title_full_unstemmed Aorta Measurements are Heritable and Influenced by Bicuspid Aortic Valve
title_short Aorta Measurements are Heritable and Influenced by Bicuspid Aortic Valve
title_sort aorta measurements are heritable and influenced by bicuspid aortic valve
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3268614/
https://www.ncbi.nlm.nih.gov/pubmed/22303356
http://dx.doi.org/10.3389/fgene.2011.00061
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