TY - JOUR
T1 - Unraveling changes in myocardial contractility during human fetal growth
T2 - A finite element analysis based on in vivo ultrasound measurements
AU - Peña, E.
AU - Tracqui, P.
AU - Azancot, A.
AU - Doblare, M.
AU - Ohayon, J.
N1 - Funding Information:
The authors thank Dr. Pierre-Simon Jouk (Department of Paediatric and Fetal Cardiology, Grenoble Hospital, France) and Y. Usson (TIMC Laboratory, Grenoble, France) for their useful discussions. Grants: The authors gratefully acknowledge research support from the European Community through the Sixth Framework Program through the DISHEART project FP6-2002-SME-1-513226 and the Spanish Ministry of Science and Technology through research projects DPI2007-63254, DPI2007-65601-C03-00, and SINBAD PSE-010000-2008, and the Instituto de Salud Carlos III (ISCIII) through the CIBER initiative. We thank also the Europe Program of Grants developed by Caja de Ahorros de la Inmaculada (CAI) and Diputación General de Aragón for their financial support to E. Peña.
PY - 2010/8
Y1 - 2010/8
N2 - Knowledge of normal fetal heart (FH) performance and development is crucial for evaluating and understanding how various congenital heart lesions may modify heart contractility during the gestational period. However, since biomechanical models of FH are still lacking, structural approaches proposed to describe the mechanical behavior of the adult human heart cannot be used to model the evolution of the FH. In this paper, a finite element model of the healthy FH wall is developed to quantify its mechanical properties during the gestational period. An idealized thickwalled ellipsoidal shape was used to model the left ventricle (LV). The diastolic LV geometry was reconstructed from in vivo ultrasound measurements performed on 24 normal FHs between 20 and 37 weeks of gestation. An anisotropic hyperelastic constitutive law describing the mechanical properties of the passive and active myocardium was used. The evolution of the mechanical properties of the normal LV myocardium during fetal growth was obtained by successfully fitting the ejection fraction predicted by the model to in vivo measurements. We found that only the active tension varies significantly during the gestational period, increasing linearly from 20 kPa (at 20 weeks) to 40 kPa (at 37 weeks of gestation). We propose a possible explanation of the increasing force-generating ability of the myocardial tissue during fetal heart development based on a combination of myocyte enlargement, differentiation, and proliferation kinetics.
AB - Knowledge of normal fetal heart (FH) performance and development is crucial for evaluating and understanding how various congenital heart lesions may modify heart contractility during the gestational period. However, since biomechanical models of FH are still lacking, structural approaches proposed to describe the mechanical behavior of the adult human heart cannot be used to model the evolution of the FH. In this paper, a finite element model of the healthy FH wall is developed to quantify its mechanical properties during the gestational period. An idealized thickwalled ellipsoidal shape was used to model the left ventricle (LV). The diastolic LV geometry was reconstructed from in vivo ultrasound measurements performed on 24 normal FHs between 20 and 37 weeks of gestation. An anisotropic hyperelastic constitutive law describing the mechanical properties of the passive and active myocardium was used. The evolution of the mechanical properties of the normal LV myocardium during fetal growth was obtained by successfully fitting the ejection fraction predicted by the model to in vivo measurements. We found that only the active tension varies significantly during the gestational period, increasing linearly from 20 kPa (at 20 weeks) to 40 kPa (at 37 weeks of gestation). We propose a possible explanation of the increasing force-generating ability of the myocardial tissue during fetal heart development based on a combination of myocyte enlargement, differentiation, and proliferation kinetics.
KW - Anisotropic hyperelasticity
KW - Fetal heart
KW - Mechanical properties
KW - Myocardium contractility
KW - Myocyte differentiation
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U2 - 10.1007/s10439-010-0010-x
DO - 10.1007/s10439-010-0010-x
M3 - Article
C2 - 20309735
AN - SCOPUS:77955173612
SN - 0090-6964
VL - 38
SP - 2702
EP - 2715
JO - Annals of Biomedical Engineering
JF - Annals of Biomedical Engineering
IS - 8
ER -