Computational Modeling of Blood Flow Hemodynamics for Biomechanical Investigation of Cardiac Development and Disease

The heart is the first functional organ in a developing embryo. Cardiac development continues throughout developmental stages while the heart goes through a serious of drastic morphological changes. Previous animal experiments as well as clinical observations showed that disturbed hemodynamics inter...

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Main Authors: Huseyin Enes Salman, Huseyin Cagatay Yalcin
Format: Article
Language:English
Published: MDPI AG 2021-01-01
Series:Journal of Cardiovascular Development and Disease
Subjects:
Online Access:https://www.mdpi.com/2308-3425/8/2/14
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spelling doaj-9188f5232b32452a8326034fc6327b502021-02-01T00:03:34ZengMDPI AGJournal of Cardiovascular Development and Disease2308-34252021-01-018141410.3390/jcdd8020014Computational Modeling of Blood Flow Hemodynamics for Biomechanical Investigation of Cardiac Development and DiseaseHuseyin Enes Salman0Huseyin Cagatay Yalcin1Department of Mechanical Engineering, TOBB University of Economics and Technology, Ankara 06530, TurkeyBiomedical Research Center, Qatar University, Doha P.O. Box 2713, QatarThe heart is the first functional organ in a developing embryo. Cardiac development continues throughout developmental stages while the heart goes through a serious of drastic morphological changes. Previous animal experiments as well as clinical observations showed that disturbed hemodynamics interfere with the development of the heart and leads to the formation of a variety of defects in heart valves, heart chambers, and blood vessels, suggesting that hemodynamics is a governing factor for cardiogenesis, and disturbed hemodynamics is an important source of congenital heart defects. Therefore, there is an interest to image and quantify the flowing blood through a developing heart. Flow measurement in embryonic fetal heart can be performed using advanced techniques such as magnetic resonance imaging (MRI) or echocardiography. Computational fluid dynamics (CFD) modeling is another approach especially useful when the other imaging modalities are not available and in-depth flow assessment is needed. The approach is based on numerically solving relevant physical equations to approximate the flow hemodynamics and tissue behavior. This approach is becoming widely adapted to simulate cardiac flows during the embryonic development. While there are few studies for human fetal cardiac flows, many groups used zebrafish and chicken embryos as useful models for elucidating normal and diseased cardiogenesis. In this paper, we explain the major steps to generate CFD models for simulating cardiac hemodynamics in vivo and summarize the latest findings on chicken and zebrafish embryos as well as human fetal hearts.https://www.mdpi.com/2308-3425/8/2/14mechanobiologybiomechanicscomputational fluid dynamicsfluid–structure interactionchicken embryozebrafish embryo
collection DOAJ
language English
format Article
sources DOAJ
author Huseyin Enes Salman
Huseyin Cagatay Yalcin
spellingShingle Huseyin Enes Salman
Huseyin Cagatay Yalcin
Computational Modeling of Blood Flow Hemodynamics for Biomechanical Investigation of Cardiac Development and Disease
Journal of Cardiovascular Development and Disease
mechanobiology
biomechanics
computational fluid dynamics
fluid–structure interaction
chicken embryo
zebrafish embryo
author_facet Huseyin Enes Salman
Huseyin Cagatay Yalcin
author_sort Huseyin Enes Salman
title Computational Modeling of Blood Flow Hemodynamics for Biomechanical Investigation of Cardiac Development and Disease
title_short Computational Modeling of Blood Flow Hemodynamics for Biomechanical Investigation of Cardiac Development and Disease
title_full Computational Modeling of Blood Flow Hemodynamics for Biomechanical Investigation of Cardiac Development and Disease
title_fullStr Computational Modeling of Blood Flow Hemodynamics for Biomechanical Investigation of Cardiac Development and Disease
title_full_unstemmed Computational Modeling of Blood Flow Hemodynamics for Biomechanical Investigation of Cardiac Development and Disease
title_sort computational modeling of blood flow hemodynamics for biomechanical investigation of cardiac development and disease
publisher MDPI AG
series Journal of Cardiovascular Development and Disease
issn 2308-3425
publishDate 2021-01-01
description The heart is the first functional organ in a developing embryo. Cardiac development continues throughout developmental stages while the heart goes through a serious of drastic morphological changes. Previous animal experiments as well as clinical observations showed that disturbed hemodynamics interfere with the development of the heart and leads to the formation of a variety of defects in heart valves, heart chambers, and blood vessels, suggesting that hemodynamics is a governing factor for cardiogenesis, and disturbed hemodynamics is an important source of congenital heart defects. Therefore, there is an interest to image and quantify the flowing blood through a developing heart. Flow measurement in embryonic fetal heart can be performed using advanced techniques such as magnetic resonance imaging (MRI) or echocardiography. Computational fluid dynamics (CFD) modeling is another approach especially useful when the other imaging modalities are not available and in-depth flow assessment is needed. The approach is based on numerically solving relevant physical equations to approximate the flow hemodynamics and tissue behavior. This approach is becoming widely adapted to simulate cardiac flows during the embryonic development. While there are few studies for human fetal cardiac flows, many groups used zebrafish and chicken embryos as useful models for elucidating normal and diseased cardiogenesis. In this paper, we explain the major steps to generate CFD models for simulating cardiac hemodynamics in vivo and summarize the latest findings on chicken and zebrafish embryos as well as human fetal hearts.
topic mechanobiology
biomechanics
computational fluid dynamics
fluid–structure interaction
chicken embryo
zebrafish embryo
url https://www.mdpi.com/2308-3425/8/2/14
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