TY - JOUR
T1 - Non-invasive Model-Based Assessment of Passive Left-Ventricular Myocardial Stiffness in Healthy Subjects and in Patients with Non-ischemic Dilated Cardiomyopathy
AU - Hadjicharalambous, Myrianthi
AU - Asner, Liya
AU - Chabiniok, Radomir
AU - Sammut, Eva
AU - Wong, James
AU - Peressutti, Devis
AU - Kerfoot, Eric
AU - King, Andrew
AU - Lee, Jack
AU - Razavi, Reza
AU - Smith, Nicolas
AU - Carr-White, Gerald
AU - Nordsletten, David
N1 - Funding Information:
The authors would like to acknowledge the funding from the BHF New Horizons program (NH/11/5/29058) and by Engineering and Physical Sciences Research Council (EP/H046410/1 and EP/N011554/1). The research was in part supported by the NIHR Biomedical Research Centre (BRC) based at Guy's and St Thomas' NHS Foundation Trust and King's College London and by the Wellcome Trust-EPSRC Centre of Excellence in Medical Engineering (WT 088641/Z/09/Z). The Image Registration Toolkit (IRTK) was used under Licence from Ixico Ltd. The views expressed are those of the authors and not necessarily those of the NHS, the NIHR, or the DoH.
Publisher Copyright:
© 2016, The Author(s).
PY - 2017/3/1
Y1 - 2017/3/1
N2 - Patient-specific modelling has emerged as a tool for studying heart function, demonstrating the potential to provide non-invasive estimates of tissue passive stiffness. However, reliable use of model-derived stiffness requires sufficient model accuracy and unique estimation of model parameters. In this paper we present personalised models of cardiac mechanics, focusing on improving model accuracy, while ensuring unique parametrisation. The influence of principal model uncertainties on accuracy and parameter identifiability was systematically assessed in a group of patients with dilated cardiomyopathy (n= 3) and healthy volunteers (n= 5). For all cases, we examined three circumferentially symmetric fibre distributions and two epicardial boundary conditions. Our results demonstrated the ability of data-derived boundary conditions to improve model accuracy and highlighted the influence of the assumed fibre distribution on both model fidelity and stiffness estimates. The model personalisation pipeline—based strictly on non-invasive data—produced unique parameter estimates and satisfactory model errors for all cases, supporting the selected model assumptions. The thorough analysis performed enabled the comparison of passive parameters between volunteers and dilated cardiomyopathy patients, illustrating elevated stiffness in diseased hearts.
AB - Patient-specific modelling has emerged as a tool for studying heart function, demonstrating the potential to provide non-invasive estimates of tissue passive stiffness. However, reliable use of model-derived stiffness requires sufficient model accuracy and unique estimation of model parameters. In this paper we present personalised models of cardiac mechanics, focusing on improving model accuracy, while ensuring unique parametrisation. The influence of principal model uncertainties on accuracy and parameter identifiability was systematically assessed in a group of patients with dilated cardiomyopathy (n= 3) and healthy volunteers (n= 5). For all cases, we examined three circumferentially symmetric fibre distributions and two epicardial boundary conditions. Our results demonstrated the ability of data-derived boundary conditions to improve model accuracy and highlighted the influence of the assumed fibre distribution on both model fidelity and stiffness estimates. The model personalisation pipeline—based strictly on non-invasive data—produced unique parameter estimates and satisfactory model errors for all cases, supporting the selected model assumptions. The thorough analysis performed enabled the comparison of passive parameters between volunteers and dilated cardiomyopathy patients, illustrating elevated stiffness in diseased hearts.
KW - Model uncertainties
KW - Myocardium
KW - Parameter uniqueness
KW - Patient-specific modelling
KW - Stiffness
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U2 - 10.1007/s10439-016-1721-4
DO - 10.1007/s10439-016-1721-4
M3 - Article
C2 - 27605213
AN - SCOPUS:84986247213
SN - 0090-6964
VL - 45
SP - 605
EP - 618
JO - Annals of Biomedical Engineering
JF - Annals of Biomedical Engineering
IS - 3
ER -