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Elastin-Dependent Aortic Heart Valve Leaflet Curvature Changes During Cyclic Flexure

The progression of calcific aortic valve disease (CAVD) is characterized by extracellular matrix (ECM) remodeling, leading to structural abnormalities and improper valve function. The focus of the present study was to relate aortic valve leaflet axial curvature changes as a function of elastin degra...

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Autores principales: Tesfamariam, Melake D., Mirza, Asad M., Chaparro, Daniel, Ali, Ahmed Z., Montalvan, Rachel, Saytashev, Ilyas, Gonzalez, Brittany A., Barreto, Amanda, Ramella-Roman, Jessica, Hutcheson, Joshua D., Ramaswamy, Sharan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6631801/
https://www.ncbi.nlm.nih.gov/pubmed/31067726
http://dx.doi.org/10.3390/bioengineering6020039
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author Tesfamariam, Melake D.
Mirza, Asad M.
Chaparro, Daniel
Ali, Ahmed Z.
Montalvan, Rachel
Saytashev, Ilyas
Gonzalez, Brittany A.
Barreto, Amanda
Ramella-Roman, Jessica
Hutcheson, Joshua D.
Ramaswamy, Sharan
author_facet Tesfamariam, Melake D.
Mirza, Asad M.
Chaparro, Daniel
Ali, Ahmed Z.
Montalvan, Rachel
Saytashev, Ilyas
Gonzalez, Brittany A.
Barreto, Amanda
Ramella-Roman, Jessica
Hutcheson, Joshua D.
Ramaswamy, Sharan
author_sort Tesfamariam, Melake D.
collection PubMed
description The progression of calcific aortic valve disease (CAVD) is characterized by extracellular matrix (ECM) remodeling, leading to structural abnormalities and improper valve function. The focus of the present study was to relate aortic valve leaflet axial curvature changes as a function of elastin degradation, which has been associated with CAVD. Circumferential rectangular strips (L × W = 10 × 2.5 mm) of normal and elastin-degraded (via enzymatic digestion) porcine AV leaflets were subjected to cyclic flexure (1 Hz). A significant increase in mean curvature (p < 0.05) was found in elastin-degraded leaflet specimens in comparison to un-degraded controls at both the semi-constrained (50% of maximum flexed state during specimen bending and straightening events) and fully-constrained (maximally-flexed) states. This significance did not occur in all three flexed configurations when measurements were performed using either minimum or maximum curvature. Moreover, the mean curvature increase in the elastin-degraded leaflets was most pronounced at the instance of maximum flexure, compared to un-degraded controls. We conclude that the mean axial curvature metric can detect distinct spatial changes in aortic valve ECM arising from the loss in bulk content and/or structure of elastin, particularly when there is a high degree of tissue bending. Therefore, the instance of maximum leaflet flexure during the cardiac cycle could be targeted for mean curvature measurements and serve as a potential biomarker for elastin degradation in early CAVD remodeling.
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spelling pubmed-66318012019-08-19 Elastin-Dependent Aortic Heart Valve Leaflet Curvature Changes During Cyclic Flexure Tesfamariam, Melake D. Mirza, Asad M. Chaparro, Daniel Ali, Ahmed Z. Montalvan, Rachel Saytashev, Ilyas Gonzalez, Brittany A. Barreto, Amanda Ramella-Roman, Jessica Hutcheson, Joshua D. Ramaswamy, Sharan Bioengineering (Basel) Article The progression of calcific aortic valve disease (CAVD) is characterized by extracellular matrix (ECM) remodeling, leading to structural abnormalities and improper valve function. The focus of the present study was to relate aortic valve leaflet axial curvature changes as a function of elastin degradation, which has been associated with CAVD. Circumferential rectangular strips (L × W = 10 × 2.5 mm) of normal and elastin-degraded (via enzymatic digestion) porcine AV leaflets were subjected to cyclic flexure (1 Hz). A significant increase in mean curvature (p < 0.05) was found in elastin-degraded leaflet specimens in comparison to un-degraded controls at both the semi-constrained (50% of maximum flexed state during specimen bending and straightening events) and fully-constrained (maximally-flexed) states. This significance did not occur in all three flexed configurations when measurements were performed using either minimum or maximum curvature. Moreover, the mean curvature increase in the elastin-degraded leaflets was most pronounced at the instance of maximum flexure, compared to un-degraded controls. We conclude that the mean axial curvature metric can detect distinct spatial changes in aortic valve ECM arising from the loss in bulk content and/or structure of elastin, particularly when there is a high degree of tissue bending. Therefore, the instance of maximum leaflet flexure during the cardiac cycle could be targeted for mean curvature measurements and serve as a potential biomarker for elastin degradation in early CAVD remodeling. MDPI 2019-05-07 /pmc/articles/PMC6631801/ /pubmed/31067726 http://dx.doi.org/10.3390/bioengineering6020039 Text en © 2019 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Tesfamariam, Melake D.
Mirza, Asad M.
Chaparro, Daniel
Ali, Ahmed Z.
Montalvan, Rachel
Saytashev, Ilyas
Gonzalez, Brittany A.
Barreto, Amanda
Ramella-Roman, Jessica
Hutcheson, Joshua D.
Ramaswamy, Sharan
Elastin-Dependent Aortic Heart Valve Leaflet Curvature Changes During Cyclic Flexure
title Elastin-Dependent Aortic Heart Valve Leaflet Curvature Changes During Cyclic Flexure
title_full Elastin-Dependent Aortic Heart Valve Leaflet Curvature Changes During Cyclic Flexure
title_fullStr Elastin-Dependent Aortic Heart Valve Leaflet Curvature Changes During Cyclic Flexure
title_full_unstemmed Elastin-Dependent Aortic Heart Valve Leaflet Curvature Changes During Cyclic Flexure
title_short Elastin-Dependent Aortic Heart Valve Leaflet Curvature Changes During Cyclic Flexure
title_sort elastin-dependent aortic heart valve leaflet curvature changes during cyclic flexure
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6631801/
https://www.ncbi.nlm.nih.gov/pubmed/31067726
http://dx.doi.org/10.3390/bioengineering6020039
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