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Towards Personalized Cardiology: Multi-Scale Modeling of the Failing Heart

  • Elham Kayvanpour ,

    Contributed equally to this work with: Elham Kayvanpour, Tommaso Mansi, Farbod Sedaghat-Hamedani

    Affiliations Department of Medicine III, University of Heidelberg, Heidelberg, Germany, DZHK (German Centre for Cardiovascular Research), Heidelberg, Germany

  • Tommaso Mansi ,

    Contributed equally to this work with: Elham Kayvanpour, Tommaso Mansi, Farbod Sedaghat-Hamedani

    Affiliation Siemens Corporation, Corporate Technology, Imaging and Computer Vision, Princeton, New Jersey, United States of America

  • Farbod Sedaghat-Hamedani ,

    Contributed equally to this work with: Elham Kayvanpour, Tommaso Mansi, Farbod Sedaghat-Hamedani

    Affiliations Department of Medicine III, University of Heidelberg, Heidelberg, Germany, DZHK (German Centre for Cardiovascular Research), Heidelberg, Germany

  • Ali Amr,

    Affiliations Department of Medicine III, University of Heidelberg, Heidelberg, Germany, DZHK (German Centre for Cardiovascular Research), Heidelberg, Germany

  • Dominik Neumann,

    Affiliation Siemens Corporation, Corporate Technology, Imaging and Computer Vision, Princeton, New Jersey, United States of America

  • Bogdan Georgescu,

    Affiliation Siemens Corporation, Corporate Technology, Imaging and Computer Vision, Princeton, New Jersey, United States of America

  • Philipp Seegerer,

    Affiliation Siemens Corporation, Corporate Technology, Imaging and Computer Vision, Princeton, New Jersey, United States of America

  • Ali Kamen,

    Affiliation Siemens Corporation, Corporate Technology, Imaging and Computer Vision, Princeton, New Jersey, United States of America

  • Jan Haas,

    Affiliations Department of Medicine III, University of Heidelberg, Heidelberg, Germany, DZHK (German Centre for Cardiovascular Research), Heidelberg, Germany

  • Karen S. Frese,

    Affiliations Department of Medicine III, University of Heidelberg, Heidelberg, Germany, DZHK (German Centre for Cardiovascular Research), Heidelberg, Germany

  • Maria Irawati,

    Affiliation Department of Medicine III, University of Heidelberg, Heidelberg, Germany

  • Emil Wirsz,

    Affiliation Siemens AG, Corporate Technology, Erlangen, Germany

  • Vanessa King,

    Affiliation Siemens Corporation, Corporate Technology, Sensor Technologies, Princeton, New Jersey, United States of America

  • Sebastian Buss,

    Affiliation Department of Medicine III, University of Heidelberg, Heidelberg, Germany

  • Derliz Mereles,

    Affiliation Department of Medicine III, University of Heidelberg, Heidelberg, Germany

  • Edgar Zitron,

    Affiliation Department of Medicine III, University of Heidelberg, Heidelberg, Germany

  • Andreas Keller,

    Affiliations Biomarker Discovery Center Heidelberg, Heidelberg, Germany, Department of Human Genetics, Saarland University, Homburg, Germany

  • Hugo A. Katus,

    Affiliations Department of Medicine III, University of Heidelberg, Heidelberg, Germany, DZHK (German Centre for Cardiovascular Research), Heidelberg, Germany, Klaus Tschira Institute for Computational Cardiology, Heidelberg, Germany

  • Dorin Comaniciu,

    Affiliation Siemens Corporation, Corporate Technology, Imaging and Computer Vision, Princeton, New Jersey, United States of America

  •  [ ... ],
  • Benjamin Meder

    Benjamin.Meder@med.uni-heidelberg.de

    Affiliations Department of Medicine III, University of Heidelberg, Heidelberg, Germany, DZHK (German Centre for Cardiovascular Research), Heidelberg, Germany, Klaus Tschira Institute for Computational Cardiology, Heidelberg, Germany

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Towards Personalized Cardiology: Multi-Scale Modeling of the Failing Heart

  • Elham Kayvanpour, 
  • Tommaso Mansi, 
  • Farbod Sedaghat-Hamedani, 
  • Ali Amr, 
  • Dominik Neumann, 
  • Bogdan Georgescu, 
  • Philipp Seegerer, 
  • Ali Kamen, 
  • Jan Haas, 
  • Karen S. Frese
PLOS
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Abstract

Background

Despite modern pharmacotherapy and advanced implantable cardiac devices, overall prognosis and quality of life of HF patients remain poor. This is in part due to insufficient patient stratification and lack of individualized therapy planning, resulting in less effective treatments and a significant number of non-responders.

Methods and Results

State-of-the-art clinical phenotyping was acquired, including magnetic resonance imaging (MRI) and biomarker assessment. An individualized, multi-scale model of heart function covering cardiac anatomy, electrophysiology, biomechanics and hemodynamics was estimated using a robust framework. The model was computed on n=46 HF patients, showing for the first time that advanced multi-scale models can be fitted consistently on large cohorts. Novel multi-scale parameters derived from the model of all cases were analyzed and compared against clinical parameters, cardiac imaging, lab tests and survival scores to evaluate the explicative power of the model and its potential for better patient stratification. Model validation was pursued by comparing clinical parameters that were not used in the fitting process against model parameters.

Conclusion

This paper illustrates how advanced multi-scale models can complement cardiovascular imaging and how they could be applied in patient care. Based on obtained results, it becomes conceivable that, after thorough validation, such heart failure models could be applied for patient management and therapy planning in the future, as we illustrate in one patient of our cohort who received CRT-D implantation.

Introduction

Systolic HF is a leading cause of hospitalization in developed countries. Its prevalence is estimated to increase by 25% till 2030 [1], with an associated health care expenditure increase of 120% in the same period. HF can be the result of a variety of underlying conditions, including ischemic, genetic and inflammatory cardiomyopathy, hypertension, metabolic diseases or toxic injury [2, 3]. Currently, guideline-based therapies of HF rely mainly on the stage of the disease depending on patients’ symptoms, cardiac performance as assessed by imaging modalities, and few objective biomarkers, but rather neglect individual factors regarding disease etiology and prognosis. Although survival of systolic HF patients has improved over the past decades, morbidity and mortality rates are still unacceptably high. To improve survival, new clinical scores, molecular biomarkers and image-based technologies are required for more precise classification of disease stages and calculation of the individual risk [4].

The past decades have seen a tremendous research effort in the computational modeling of cardiac function [522]. While they were first developed for biology and disease understanding [5, 6, 8, 13, 23], these models are now maturing towards clinical application [5, 7, 1012, 14, 22, 2429]. This included the identification of the mathematical laws underlying biological mechanisms such as cardiac electrophysiology, biomechanics, or hemodynamics, all of which have been derived or verified using experimental data. Later, multi-scale mathematical frameworks have been developed to simulate the cardiac function at the whole-organ scale [6, 7, 9, 14, 15, 24, 30]. One challenge for a clinical use remained the issue of personalization from patients’ clinical images and data, which is now one of the main research interests of the scientific community (see for instance [7, 11, 14, 15, 22, 24, 31]). Hence, a large-scale evaluation is still missing due to the complexity of the personalization algorithms (from anatomy to function) and the required computational power of the models.

In this study, we developed a multi-scale model of HF and explored if it can provide new insights on HF patients in a sufficiently large population. In particular, computationally efficient models coupled with robust parameter estimation methods are employed to estimate an individualized model on 46 HF cases. We show for the first time that estimated model parameters from imaging are very consistent with cardiac imaging, lab tests and prognosis scores. Because the employed multi-scale computational model is predictive, we also illustrate in one case its potential in personalized planning of cardiac resynchronization therapy.

Methods

Clinical Workflow and Patient Recruitment

The present study has been approved by the ethics committee, medical faculty of Heidelberg and participants have given written informed consent. In this case-only study, 46 patients were included with diagnosis of non-ischemic systolic HF and underwent diagnostic coronary angiography, echocardiography, cMRI, comprehensive clinical phenotyping and biomarker measurements for the evaluation of a newly HF onset. The majority of patients also received invasive hemodynamic assessment (left circulation in 43 (93%) cases, right circulation in 37 (80%) cases). To capture all stages of systolic heart failure, we also included symptomatic patients with only slightly decreased systolic performance in the initial assessment of cardiac function by echocardiography or ventricular angiography (LV-EF <55%). All patients showed signs or symptoms of HF (e.g. breathlessness, reduced walking capacity, ankle swelling or pulmonary crackles) [3]. Patients with relevant CAD, valvular heart disease, acute myocarditis or a history of cardiotoxic chemotherapy were excluded.

Patient-Specific Computational Model of Human Non-ischemic Systolic Heart Failure

For each patient of the cohort (n = 46), a multi-scale, multi-physics model of cardiac function was estimated based on the pseudonymized imaging data, 12-lead ECG and invasive pressure catheterization [31]. Heart anatomy [32], electrophysiology [22, 31], hemodynamics and biomechanics [31, 33] were modeled (Fig 1). Each of these components is personalized to fit the observed physiology of the patient [31]. An overview of the approach is described in this section. The reader is referred to the cited references for more details due to lack of space.

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Fig 1. Overview of the modeling pipeline, from clinical data (input) to multi-scale, multi-physics cardiac models (output).

The framework components are described in detail in methods.

http://dx.doi.org/10.1371/journal.pone.0134869.g001

Anatomy.

First a detailed model of the bi-ventricular myocardium is generated. The myocardium is segmented under expert guidance from short-axis cine cMRI. The model includes the left and right endocardia, LV outflow tract, RV inflow and outflow tracts, and LV epicardium. Each of these components is estimated consistently and simultaneously using a machine-learning approach [32] and verified by an expert. In brief, the algorithm is trained from a large database of annotated cine cMRI to automatically detect the heart position, rotation and scale in the image. Each step is learned using the Marginal Space Learning framework and Probabilistic Boosting Trees [32]. A boundary detector is also learned from the database to recognize myocardium contours in the images. On unseen data, the algorithm first uses the location detectors to find the heart at the end-diastole time frame, and then fits a mean heart shape model whose contours are finally deformed according to the boundary detectors to match the myocardium boundaries. Once the model is detected, it is tracked over time using a symmetric image registration algorithm [34]. An expert then carefully verifies the tracked contours and edits them interactively if needed. Blood pool volume is finally computed at each time instant from the anatomical model.

Next, the surfaces of each component at end diastole are fused to form a unified, volumetric model of the bi-ventricular myocardium. As the RV epicardium is hardly visible in the cMRI, a standard thickness of 3mm is applied. The surface of the volumetric model is labeled as LV (left endocardium), RV (right endocardium), LV septum and RV septum based on the original segmentation [14, 33]. Finally, a model of fiber architecture is generated following a rule-based approach [13]. In this study, LV elevation angles vary linearly from -60° to the epicardium to 0° to the mid-wall to 60° to the endocardium, RV elevation angles vary from -80° to 80°.

Electrophysiology.

Patient cardiac electrophysiology (EP) is computed using a reaction-diffusion equation, so-called mono-domain equation, which models the dynamics of the trans-membrane potential and its diffusion throughout the myocardial tissue. In this study, the Mitchell and Schaeffer (M-S) model of the trans-membrane potential is employed [35]. Contrary to more complex ionic models, which consider the ionic interactions through a large number of transmembrane channels [36], the M-S model captures the bulk inflow and outflow ionic exchanges as described in [35]. Despite its simplified formulation, M-S model has shown good behavior in pathological situations, in particular alternans, arrhythmias and wave re-entries [15, 35, 37]. The M-S model is controlled by four parameters, which have a direct impact on the dynamics of the action potential and the restitution curve. In particular, the duration of the action potential is directly controlled by the parameter τc, which is related to the QT duration in the ECG. The other parameters (τopen, τin and τout), which control the diastolic interval and the restitution curve, are kept to their default values in this study [35]. The computed potential is then diffused throughout the myocardial tissue according to the electrical conductivity, tissue anisotropy defined by the cardiac fibers and cardiac activation pathways [22, 37]. The electrical signal starts at the LV and RV septum (His bundle). A thin, 1mm-thick sub-endocardial layer is defined to mimic the Purkinje system, with two different electrical conductivities for the left and right ventricle Purkinje systems (cLV and cRV respectively). The rest of the myocardium is modeled with a slower electrical conductivity cMyo [22]. To cope with tissue anisotropy, the electrical conductivity is assumed to be nine times higher along the fibers (equivalent to a fiber speed three times faster than cross-fiber). The model is solved on the patient heart anatomy by using a novel framework based on the Lattice-Boltzmann method (LBM-EP) [37], which allows near real-time computations. Finally, torso potentials are calculated using the boundary element methods (BEM) as described in [22], from which 12-lead ECG signals are calculated and displayed to the user. To cope with the lack of full-torso images, a patient-specific torso model was obtained as follows. A torso atlas was first registered to the cMRI scout images acquired in axial, sagittal and coronal views. The heart of the torso atlas was rigidly aligned with the heart of the patient. The torso surface was then deformed using an affine transformation to match the patient torso boundaries visible in the scouting images [22]. ECG leads were then placed at their clinical locations on the individualized torso model. In [22], the properties of the coupled heart-torso EP model were extensively investigated and validated against numerical experiments, while computational efficiency and scalability was explored in [38].

The personalization of the EP model is performed in three steps, as described in details in [39]. First, myocardium conductivity (cMyo) is automatically estimated using inverse modeling. To this end, the NEWUOA algorithm [40], a gradient-free optimization method, is used such that computed QRS duration (cQRSd) matches the mQRSd measured in the ECG signal. Next, LV and RV subendocardial conductivity, cLA and cRV, are estimated to capture the measured electrical axis (EA). Finally, the value of the parameter τc is directly inferred from the QT interval. These three steps are iterated until convergence is reached (generally after two or three iterations). This fitting procedure is done only once per patient: at the end of it, the current state of patient cardiac electrophysiology is captured.

Biomechanics.

The cardiac motion resulting from the electrophysiology computed as previously described is calculated according to a multi-scale biomechanical model of the cardiac tissue [31, 33]. More precisely, a two-element Hill model is employed. The passive properties of the myocardium are modeled as isotropic linear elastic tissue. A co-rotational implementation is employed to correctly capture the large deformations and rotations during systole [41]. Tissue elasticity is parameterized by the Young’s modulus E and estimated from the images as described below. Incompressibility is ensured by setting the Poisson ratio υ to 0.48 for all cases in this study. A phenomenological model of the active force generated during systole is coupled to the passive model [14, 42]. The force is timed according to the electrophysiology while its maximal amplitude is controlled by the maximum active force parameter σ. The force increases and decreases according to an exponential law with two different decay parameters, kATP and kRS, related to ATP binding and myosin head release rates [42]. The heart is fixed in space using a contact-based pericardium force, defined as the epicardial bag at end-diastole [43], and a basis stiffness constraint, modeled as springs attached around each of the four cardiac valves to mimic the ventricular attachment to the artery and atria. Both parameters E and σ can be set regionally. In particular, LV E and σ are estimated automatically for each patient by minimizing the sum of the squared differences between computed and measured ejection fraction (EF), stroke volume (SV), end-diastolic volume (EDV), end-systolic volume (ESV), end-diastolic pressure (EDP) and end-systolic pressure (ESP). As for the EP component, the minimization is performed using NEWUOA optimizer, as described in [31, 40], and done only once for each case.

Hemodynamics.

Finally, the biomechanical model is coupled with a lumped model of intra-cardiac hemodynamics to capture the pre-load and post-load conditions of the patients [14, 23, 33]. The four cardiac phases are calculated (filling, isovolumetric contraction, ejection, isovolumetric relaxation). A well-validated 3-element Windkessel model is employed to model the arteries [44], whose parameters (artery compliance C, peripheral resistance Rp, characteristic resistance Rc and remote pressure pr) are estimated from the arterial pressure catheterization measurement and the MRI-based blood flow measurement using an optimization approach [31]. The lumped model of atrial contraction presented in [23] is also used. The ventricular pressure is calculated such that the isovolumetric constraint is ensured through a prediction-correction scheme as described in [33]. The phases are fully controlled by the electrophysiology (which triggers cardiac contraction) and hemodynamics load. In this study, no circulatory system was used contrary to [23], the two ventricles were not hemodynamically connected between each other. Although this could be a limitation to capture adaptation to pulmonary or systemic hypertension for instance, such a simplification showed promising results in heart failure modeling and cardiac resynchronization therapy, as highlighted by recent results reported by other groups [7, 14]. The complete biomechanical model is implemented in SOFA, an open-source simulation framework [45].

On a standard desktop machine (Intel Xeon E5629, 2.40GHz, NVidia GeForce GTX580 card, 4GB RAM), segmenting the chambers takes from 2–3s to 2–3 minutes per frame depending on the level of editing required, building the anatomical model takes 1 minute (including meshing, tagging and fibers, all steps being automatic), the forward EP computation takes 5s, the forward EM computation takes 3 minutes. The personalization procedure, which requires several forward model estimations, takes between 3 to 4 hours per patient. Overall, going from the clinical data of a patient to a complete, personalized model takes approximately 3–5 hours. At each step, the user can verify the result and validate them before moving to the next step.

CRT simulation

In addition to the main contribution of this study, which is the population analysis, we also illustrate in this manuscript how such a multi-scale model could be used for cardiac resynchronization therapy planning and guidance in our cohort. The model estimation procedure described in the previous section has been designed such that the model matches the observed patient physiology. However, the estimated parameters may not be unique due to noise and sparsity in the data, and model assumptions, as quantified in [31, 46] for instance. Another way to evaluate the model is to test its predictive power after a change in the cardiac system. Indeed, even if two sets of parameters would yield the same visible cardiac motion, it is likely that only one would enable precise prediction of system changes, due to therapy for instance. We illustrate the predictive power of our framework in one patient of our cohort, who underwent CRT-D device implantation due to LV-EF<35%, left bundle branch blockage (QRSd = 124 ms) and HF NYHA class III despite optimal medical therapy. An additional 12-lead ECG recording was acquired one day after device implantation and during testing of three different stimulation protocols: biventricular pacing (BiV; LV-RV delay = 20 ms), RV only stimulation and DDT-40 LV triggered. In all three cases we acquired comprehensive echocardiography. We first fitted the model to the baseline ECG (cQRSd = 123 ms (measured = 124 ms) and EA = -17° (measured = -17°), S5A Fig). The estimated electrical conductivities were equal to 320 mm2/s, 1600 mm2/s and 2200 mm2/s for the myocardium, LV endocardium and RV endocardium, respectively. It should be noted that in this experiment the estimation aimed to capture T-wave onset timing only, but not T-wave morphology. We then reproduced the CRT on the virtual heart based on the interventional report and the applied protocols (S5B Fig).

Statistical Analysis

Statistical analyses were carried out with „R”software (version 3.0.2). Histograms were calculated using the “hist” function with standard parameters. Outliers were detected with the Grubbs test available in the “outliers” package. Correlation coefficients were assessed by the “cor” function and corresponding significance values by the “cor.test” procedure. In order to visualize the output, customized scatter plots were generated. Smoothing of scatter plots was carried out by the “smoothScatter” function included in the bioconductor “geneplotter” package. On top and right of each scatter plot, the distribution of both plotted variables was respectively drawn as box plot.

Results

Personalized multi-scale computer models are detailed representations of systolic HF

In this study, we consecutively recruited patients subjected to invasive and imaging-based diagnosis of HF. Table 1 summarizes the clinical characteristics of this study cohort, while Table 2 provides the findings of ECG and cMRI recordings. After data anonymization and curation, we transferred imaging and hemodynamic data to the developed modeling framework.

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Table 1. Clinical characteristics of the patient cohort with non-ischemic systolic HF.

http://dx.doi.org/10.1371/journal.pone.0134869.t001

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Table 2. ECG and cMRI findings of patient cohort with non-ischemic systolic HF.

http://dx.doi.org/10.1371/journal.pone.0134869.t002

Anatomy Model.

Three dimensional models of the bi-ventricular anatomy were generated from cMRI under expert guidance (Fig 2A). A considerable variability of bi-ventricular shapes could be observed across the population, with an average variation of about 5mm around a mean atlas calculated from the population [47] (Fig 2B). After heart tracking and volume computation (Fig 2C), mean left ventricle ejection fraction (LV-EF) of the computed models was 36 +/- 14%. In particular, three patients were identified having LV-EF in the normal range (≥ 55%), 10 mild reduction in LV-EF, 17 moderate LV-EF decrease and 16 had a severe dysfunction. Fig 2D shows the fiber architecture computed on the anatomical model in a typical case [30].

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Fig 2. Automated estimation of the 3D anatomical model.

A) Automatic segmentation of the right and left ventricle. B) Observed variability in cardiac anatomy (shape is color-coded on a template) estimated from the HF cohort. The representation indicates the variability in phenotypes from the cohort. C) After the different steps of the model computation are finished, computed intracardiac volume variations can be estimated. D) Fiber architecture applied to the personalized heart models.

http://dx.doi.org/10.1371/journal.pone.0134869.g002

Electrophysiology Model.

Electrical conductivity for the myocardium (cMyo), left (cLV) and right endocardia (cRV) were estimated based on the anatomical model and the QRS duration (QRSd) and electrical axis (EA) measured from the 12-lead ECG traces [31]. After personalization, computed cQRSd matched the measured mQRSd within 12 +/- 10 ms accuracy (R = 0.82, p<10−7), confirming the ability of the model to capture HF electrophysiology and the efficacy of the ECG personalization algorithm. The EA was in some cases more difficult to estimate (mean error = -23 +/- 55 degrees, R = 0.32, p<0.05), probably due to localized pathologies (e.g. bundle blocks) that was not captured by our global personalization procedure. The distribution of the estimated conductivities across the population is displayed in S1 Fig. Fig 3 shows the electrical activation and the computed ECG traces (first six leads) calculated for the same patient illustrated in Fig 1. For that example, computed QRSd, QTd and EA were equal to 172 ms, 458 ms and -42 degrees respectively, compared to the measured values of 175 ms (ΔQRS = 3ms), 456 ms (ΔQT = 2ms) and -42° (ΔEA = 0°) of the surface 12-lead ECG.

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Fig 3. Patient-specific electrophysiology computation.

Left Panels: Computed ECG traces from the model in the patient exemplarily chosen. Right Panels: Computed trans-membrane potential propagation throughout the cardiac cycle (time in % of cycle length).

http://dx.doi.org/10.1371/journal.pone.0134869.g003

Hemodynamics Model.

Patient-specific artery compliance and resistances were estimated from cMRI-derived volume curves and invasive pressure catheterization [31]. Fig 4A illustrates, again in the same case, the computed arterial pressure curves in the left (systemic) and right (pulmonary) main arteries after personalization. As one can see, the model captured the main trends of the pressure dynamics, in particular systolic and diastolic pressures. Table 3 reports descriptive statistics of the estimated artery compliance (C), peripheral resistance (Rp), characteristic resistance (Rc) and remote pressure (Pr) (histograms reported in S2 Fig). It should be noted that for the very few patients who did not have invasive pressure measurements, generic values were applied (Table A in S1 File).

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Table 3. Statistics of estimated Windkessel parameters throughout the studied population.

http://dx.doi.org/10.1371/journal.pone.0134869.t003

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Fig 4. Patient-specific hemodynamics.

A) Personalized computation of arterial flow after personalization of the Windkessel parameters. B) Measured and computed LV pressure and volume curve in one patient, showing the high concordance between the clinical and modeling data.

http://dx.doi.org/10.1371/journal.pone.0134869.g004

Biomechanical Model.

Finally, we computed cardiac electromechanics for all cases. LV stiffness E and maximum active force σ were estimated (S3 Fig) [31]. The model allowed us also to derive the time-varying ventricular volume and pressure, which we compared with the invasive measurements to further evaluate model goodness of fit (Fig 4B). Qualitatively, the fitting was judged by two independent experts to be excellent in 29 patients (i.e. perfect match of the volume and pressure curves up to the noise level), good in 15 (i.e. the main trends of the volume and pressure curves were captured, but not in all details), and sub-optimal in 2 cases (curves did not match). Quantitatively, S4 Fig shows the correlation between the cMRI-derived and model-derived LV-EF (A) and stroke volume (SV) (B), underlining the precision of the HF model in terms of global cardiac function.

Estimation of novel cardiac functional parameters using a virtual failing heart

One advantage of the multi-scale model is that it provides functional parameters that cannot be directly measured from image analysis or clinical phenotyping, potentially providing novel surrogates of HF and further insights into patient’s condition or disease stage. Table B in S1 File summarizes some of the new parameters derived from the model. To examine the clinical value of those new parameters, we performed correlation analyses (Pearson coefficient) with rich clinical phenotypes. To avoid bias in the study, only the data that was not used in the model fitting procedure were investigated.

As shown in Table 4, a good correlation was found between left ventricular active force and the systolic blood pressure after physical activity. Left ventricular active force negatively correlated with the diagnosis and prognosis biomarker NT-ProBNP. Although these correlations are still modest, they provide a first hint at the potential use in further stratifying patients, especially since they may provide unambiguous disease information.

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Table 4. Correlations between LV active force and LV stiffness and clinical presentations of patients.

http://dx.doi.org/10.1371/journal.pone.0134869.t004

To further explore a potential prognostic value, we performed correlation analyses of the unique parameters with the Seattle HF Score [48]. The Seattle HF Model predicts survival of HF patients by using a complex set of clinical characteristics such as the NYHA class, ischemic etiology, diuretic dose, left ventricular ejection fraction, systolic blood pressure, sodium, hemoglobin, percent lymphocytes, uric acid, and cholesterol. The Seattle score could be completely calculated in 40 patients at the time of their inclusion. After performing Grubb’s testing, one of 40 patients was detected as a statistical outlier and hence was excluded from the analysis. As shown in Fig 5, a highly significant correlation between LV active force σ and the Seattle 5-year score was found (R = 0.77, p = 2.7x10-5). Interestingly, this finding suggests that the maximum stress the myocardium can generate is predictive of HF outcome, the more impaired the myocardium contractility, the poorer the outcome.

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Fig 5. Correlation between Left ventricular active force and estimated outcome of the patients.

Correlation plot showing the left ventricular active force in the patients (x-axis) and their Seattle 5 Year Score (y-axis).

http://dx.doi.org/10.1371/journal.pone.0134869.g005

Computed heart models for therapy planning

As an example of application for personalized therapy, we simulated CRT using our virtual heart in one patient of our cohort. As shown in S5C Fig and Table C in S1 File, the model was able to successfully and highly accurately predict the changes in cardiac electrophysiology for different CRT stimulation protocols. It was able to predict the worsening of cardiac EP for both BiV and RV pacing modes (increased QRSd as a predictor of nonresponse [49, 50]) and also the preservation of EP function with the LV-triggered protocol. The later protocol was chosen by the independent treating electrophysiologist (independently from the model result), the patient showed 7 months after device implantation a significant improvement of clinical symptoms (NYHA III improved to NYHA II) as well as LV-EF (EF improved from 20% to 30%).

Discussion

Thanks to advanced guideline-adherent pharmaco- and device therapy of HF, mortality and hospitalization have been reduced. Yet, HF is still one of the major causes of death and societal burden, requiring novel therapies and personalized diagnostics [51]. In particular, the impact of individual, patient-specific factors is largely neglected in current therapies. The addition of personalization to the treatments recommended in current guidelines is seen as an opportunity to further improve the outcome and quality of care in HF.

Besides the search for novel drug targets and HF biomarkers, the computational modeling community has been striving to provide novel solutions in HF care in the form of generative models of heart physiology [5, 7, 1012, 14, 15, 22, 36]. The simulation of subcellular mechanisms is already possible with high fidelity compared to experimental data [30, 36, 52]. At the organ level, these simulations are far more complex, but have resulted in the development of prototypes of virtual hearts. Recent effort is now focusing on the translation of these models to the clinics [7, 14, 15]. The model presented in this study relies on validated biophysical models and numerical methods [22, 33] and combines this with a fitting framework that allowed for the first time investigation of an adequately sized cohort of clinically well-characterized HF patients [31]. Indeed, the experiments performed in this study highlighted the necessity of having computationally efficient numerical methods and streamlined, fully-integrated personalization procedures to minimize user interaction and enable efficient and reproducible workflows.

As shown in [22], the personalization approach is able to estimate one solution of the inverse problem, with a good fit to the data. We could statistically compare the estimated parameters with clinical phenotyping and imaging, thus verifying the clinical meaningfulness of these parameters. For instance, we could find that the myocardium active force, i.e. the ability of the myocardium to contract, could be an indicator of disease severity, similar to what was reported in [53] using a study on three cases.

As shown in [54], several sets of parameters could yield the same observable physiology and noise in clinical data can considerably decrease model precision. One advantage of the present study is the availability of extended phenotyping, including MRI, echocardiography, pressure catheterization and lab tests. This unique dataset helped decreasing parameter uncertainty [31], which is reflected by the highly reproducible estimation of cardiac performance when compared to measured parameters. Similarly, the sparsity of the clinical observation (12-lead ECG) yields to a significant level of uncertainty in estimated electrical conductivities, as quantified in [22]. Despite this limitation, the model was still able to predict therapy in the illustrative example reported in the results section and in [39]. The topic of parameter uncertainty is an important research area [25, 31, 46, 54], which requires further investigations.

Over the whole cohort of 46 patients, the correlation of the computed parameters to the values obtained through detailed clinical phenotyping reached promising statistical power, rendering it reasonable to derive additional parameters of cardiac function that are not directly assessable from imaging data. Given the available model, we could provide first estimates of new patient-specific parameters such as electrical conductivity, myocardial stiffness or cardiac active force in a HF cohort, which could be used in subsequent studies. While they may show some overlap with existing measures of HF severity, indicated by their correlation e.g. to natriuretic peptides, they also may provide unambiguous information about the state of an individual patient and his prognosis. Nominating these parameters as biomarker candidates, it will be interesting to validate them in independent cohorts and compare them to existing scores and measures, as we did with the Seattle HF score.

More thorough validation of predictive mathematical models of disease processes will be the key for their implementation into clinical practice. One approach is the evaluation of the predictive power of these models in terms of therapy outcome, such as cardiac resynchronization therapy (CRT). Although not the main focus of this study, we illustrate how such a model could be used for CRT planning, suggesting good predictive power in terms of acute QRS duration. From preoperative data, we calculated acute postoperative ECG and successfully compared the result with the clinical observation. Computational modeling for CRT planning has been investigated in the past [7, 12, 14, 26]. Yet, they were based on generic geometries [26], assumed the postoperative electrophysiology [14] or did not predict the resulting ECG while assuming postoperative hemodynamics [9]. Instead, in this manuscript we illustrate how cardiac electrophysiology and ECG could be predicted based on preoperative data only. Future works include a comprehensive evaluation of this aspect on a larger cohort.

Several assumptions were made in the model used in this study, which can be a limitation. First, the ECG computation assumed homogeneous tissue between the heart and the body surface, with one electrical conductivity [22]. While this simplification can have an impact on the shape of the ECG trace, numerical studies have shown that global parameters such as QRS and QT duration are minimally dependent on tissue heterogeneity and therefore justify our approach [55]. After personalization, the model precisely captured the main features of the heart’s function, such as QRS duration and QT intervals. EA was more difficult to capture. A potential reason for this limitation is the fact that cardiac electrophysiology was only globally personalized, thus missing potential localized pathological features like lines of blocks, as confirmed in recent experiments [39]. Another simplification of the model is the linear assumption of the myocardium tissue. Ex-vivo studies showed that cardiac tissue is an orthotropic, hyper-elastic material [56]. Future work includes using more advanced models including orthotropic tissue material and whole-body circulatory models for more accurate estimation of tissue properties and more realistic cardiac motion computation. First results in that direction were reported in [33, 54]. The biomechanical model was also globally fitted to the data. While this approach enabled capturing global parameters like EF and SV, regional impairments were not captured, contrary to [53]. In these cases, the global parameters might be biased to cope with the regional pathological feature.

Supporting Information

S1 Fig. Distribution of estimated electrical conductivity in the cohort.

A) In average the myocardial electrical conductivity cMyo was equal to 413 +/- 232 mm2/s. B and C) Left and right endocardial conductivity were higher as expected owing to the fast Purkinje conduction system.

doi:10.1371/journal.pone.0134869.s001

(TIFF)

S2 Fig. Distribution of estimated Windkessel parameters in the cohort.

Upper panels: Hemodynamics features of the aorta. Lower panels: Hemodynamics features of pulmonary artery. For values see also Table A in S1 File.

doi:10.1371/journal.pone.0134869.s002

(TIF)

S3 Fig. Distributions of the estimated stiffness E and active force σ in the cohort.

Average LV stiffness E is 590 ± 135 kPa and LV maximum active force σ is 295 ± 100 kPa in study population. These parameters can only be simulated and not directly measured from image sequences or clinical data.

doi:10.1371/journal.pone.0134869.s003

(TIF)

S4 Fig. Correlation between measured cardiac values from cMRI and computed ones.

A) x: computed LV-EF, y: measured LV-EF from cMRI. The distribution of both plotted variables is respectively drawn as box plot. B) x: computed LV-SV, y: measured LV-SV from cMRI.

doi:10.1371/journal.pone.0134869.s004

(TIF)

S5 Fig. Computed heart models for prediction of CRT therapy.

A) Computed ECG trace (thick blue line) overlaid on measured ECG trace before CRT implantation. As one can see, the model was able to capture the main features of the ECG trace precisely. It should be noted that it was not in the scope to capture T-wave morphology (see text for details). B) Position of the CRT leads (in green) placed on the model according to lead positions derived from orthogonal chest x-rays. C) Observed and predicted (thick blue line) ECG traces for three tested stimulation protocols. The model was able to qualitatively predict EP CRT response.

doi:10.1371/journal.pone.0134869.s005

(TIF)

S1 File.

Table A in S1 File. Default Windkessel parameter values used when pressure data was not available, see text for details. Table B in S1 File. Parameters estimated using the multi-scale heart model. Table C in S1 File. Observed and predicted ECG parameters for different CRT protocols.

doi:10.1371/journal.pone.0134869.s006

(DOC)

Author Contributions

Conceived and designed the experiments: EK TM FS-H. Performed the experiments: TM DN BG PS AK SB DM EZ. Analyzed the data: EK TM FS-H AA JH KSF MI AK. Contributed reagents/materials/analysis tools: HAK DC BM EW VK. Wrote the paper: EK FS-H HAK BM.

References

  1. 1. Moat NE, Ludman P, de Belder MA, Bridgewater B, Cunningham AD, Young CP, et al. Long-term outcomes after transcatheter aortic valve implantation in high-risk patients with severe aortic stenosis: the U.K. TAVI (United Kingdom Transcatheter Aortic Valve Implantation) Registry. J Am Coll Cardiol. 2011;58(20):2130–8. doi: 10.1016/j.jacc.2011.08.050 pmid:22019110.
  2. 2. Ackerman MJ, Priori SG, Willems S, Berul C, Brugada R, Calkins H, et al. HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies: this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA). Europace: European pacing, arrhythmias, and cardiac electrophysiology: journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology. 2011;13(8):1077–109. doi: 10.1093/europace/eur245 pmid:21810866.
  3. 3. McMurray JJ, Adamopoulos S, Anker SD, Auricchio A, Bohm M, Dickstein K, et al. ESC guidelines for the diagnosis and treatment of acute and chronic heart failure 2012: The Task Force for the Diagnosis and Treatment of Acute and Chronic Heart Failure 2012 of the European Society of Cardiology. Developed in collaboration with the Heart Failure Association (HFA) of the ESC. Eur J Heart Fail. 2012;14(8):803–69. doi: 10.1093/eurjhf/hfs105 pmid:22828712.
  4. 4. Vogel B, Keller A, Frese KS, Leidinger P, Sedaghat-Hamedani F, Kayvanpour E, et al. Multivariate miRNA signatures as biomarkers for non-ischaemic systolic heart failure. European heart journal. 2013;34(36):2812–22. doi: 10.1093/eurheartj/eht256 pmid:23864135.
  5. 5. Trayanova NA. Whole-heart modeling: applications to cardiac electrophysiology and electromechanics. Circulation research. 2011;108(1):113–28. doi: 10.1161/CIRCRESAHA.110.223610 pmid:21212393; PubMed Central PMCID: PMC3031963.
  6. 6. Hunter PJ, Borg TK. Integration from proteins to organs: the Physiome Project. Nature reviews Molecular cell biology. 2003;4(3):237–43. pmid:12612642.
  7. 7. Tobon-Gomez C, Duchateau N, Sebastian R, Marchesseau S, Camara O, Donal E, et al. Understanding the mechanisms amenable to CRT response: from pre-operative multimodal image data to patient-specific computational models. Medical & biological engineering & computing. 2013;51(11):1235–50. doi: 10.1007/s11517-013-1044-7 pmid:23430328.
  8. 8. Land S, Niederer SA, Louch WE, Sejersted OM, Smith NP. Integrating multi-scale data to create a virtual physiological mouse heart. Interface focus. 2013;3(2):20120076. doi: 10.1098/rsfs.2012.0076 pmid:24427525; PubMed Central PMCID: PMC3638477.
  9. 9. Niederer SA, Smith NP. An improved numerical method for strong coupling of excitation and contraction models in the heart. Progress in biophysics and molecular biology. 2008;96(1–3):90–111. doi: 10.1016/j.pbiomolbio.2007.08.001 pmid:17881038.
  10. 10. Campbell SG, McCulloch AD. Multi-scale computational models of familial hypertrophic cardiomyopathy: genotype to phenotype. Journal of the Royal Society, Interface / the Royal Society. 2011;8(64):1550–61. doi: 10.1098/rsif.2011.0184 pmid:21831889; PubMed Central PMCID: PMC3177620.
  11. 11. Marchesseau S, Delingette H, Sermesant M, Ayache N. Fast parameter calibration of a cardiac electromechanical model from medical images based on the unscented transform. Biomechanics and modeling in mechanobiology. 2013;12(4):815–31. doi: 10.1007/s10237-012-0446-z pmid:23064992.
  12. 12. Kerckhoffs RC, Lumens J, Vernooy K, Omens JH, Mulligan LJ, Delhaas T, et al. Cardiac resynchronization: insight from experimental and computational models. Progress in biophysics and molecular biology. 2008;97(2–3):543–61. doi: 10.1016/j.pbiomolbio.2008.02.024 pmid:18417196; PubMed Central PMCID: PMC2676869.
  13. 13. Arts T, Reneman RS, Veenstra PC. A model of the mechanics of the left ventricle. Annals of biomedical engineering. 1979;7(3–4):299–318. pmid:547767.
  14. 14. Sermesant M, Chabiniok R, Chinchapatnam P, Mansi T, Billet F, Moireau P, et al. Patient-specific electromechanical models of the heart for the prediction of pacing acute effects in CRT: a preliminary clinical validation. Medical image analysis. 2012;16(1):201–15. doi: 10.1016/j.media.2011.07.003 pmid:21920797.
  15. 15. Relan J, Chinchapatnam P, Sermesant M, Rhode K, Ginks M, Delingette H, et al. Coupled personalization of cardiac electrophysiology models for prediction of ischaemic ventricular tachycardia. pmid:Interface focus. 2011;1(3):396–407. doi: 10.1098/rsfs.2010.0041 pmid:22670209; PubMed Central PMCID: PMC3262447.
  16. 16. Nordsletten DA, Niederer SA, Nash MP, Hunter PJ, Smith NP. Coupling multi-physics models to cardiac mechanics. Progress in biophysics and molecular biology. 2011;104(1–3):77–88. doi: 10.1016/j.pbiomolbio.2009.11.001 pmid:19917304.
  17. 17. Baillargeon B, Rebelo N, Fox DD, Taylor RL, Kuhl E. The Living Heart Project: A robust and integrative simulator for human heart function. European journal of mechanics A, Solids. 2014;48:38–47. doi: 10.1016/j.euromechsol.2014.04.001 pmid:25267880; PubMed Central PMCID: PMC4175454.
  18. 18. Potse M, Krause D, Kroon W, Murzilli R, Muzzarelli S, Regoli F, et al. Patient-specific modelling of cardiac electrophysiology in heart-failure patients. Europace: European pacing, arrhythmias, and cardiac electrophysiology: journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology. 2014;16 Suppl 4:iv56–iv61. doi: 10.1093/europace/euu257 pmid:25362171; PubMed Central PMCID: PMC4217520.
  19. 19. Huntjens PR, Walmsley J, Ploux S, Bordachar P, Prinzen FW, Delhaas T, et al. Influence of left ventricular lead position relative to scar location on response to cardiac resynchronization therapy: a model study. Europace: European pacing, arrhythmias, and cardiac electrophysiology: journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology. 2014;16 Suppl 4:iv62–iv8. doi: 10.1093/europace/euu231 pmid:25362172.
  20. 20. Ashikaga H, Arevalo H, Vadakkumpadan F, Blake RC 3rd, Bayer JD, Nazarian S, et al. Feasibility of image-based simulation to estimate ablation target in human ventricular arrhythmia. Heart rhythm: the official journal of the Heart Rhythm Society. 2013;10(8):1109–16. doi: 10.1016/j.hrthm.2013.04.015 pmid:23608593; PubMed Central PMCID: PMC3735782.
  21. 21. Ng J, Jacobson JT, Ng JK, Gordon D, Lee DC, Carr JC, et al. Virtual electrophysiological study in a 3-dimensional cardiac magnetic resonance imaging model of porcine myocardial infarction. J Am Coll Cardiol. 2012;60(5):423–30. doi: 10.1016/j.jacc.2012.03.029 pmid:22633654; PubMed Central PMCID: PMC3407287.
  22. 22. Zettinig O, Mansi T, Neumann D, Georgescu B, Rapaka S, Seegerer P, et al. Data-driven estimation of cardiac electrical diffusivity from 12-lead ECG signals. Medical image analysis. 2014;18(8):1361–76. doi: 10.1016/j.media.2014.04.011 pmid:24857832.
  23. 23. Kerckhoffs RC, Neal ML, Gu Q, Bassingthwaighte JB, Omens JH, McCulloch AD. Coupling of a 3D finite element model of cardiac ventricular mechanics to lumped systems models of the systemic and pulmonic circulation. Annals of biomedical engineering. 2007;35(1):1–18. doi: 10.1007/s10439-006-9212-7 pmid:17111210; PubMed Central PMCID: PMC2872168.
  24. 24. Xi J, Lamata P, Niederer S, Land S, Shi W, Zhuang X, et al. The estimation of patient-specific cardiac diastolic functions from clinical measurements. Medical image analysis. 2013;17(2):133–46. doi: 10.1016/j.media.2012.08.001 pmid:23153619.
  25. 25. Wallman M, Smith NP, Rodriguez B. Computational methods to reduce uncertainty in the estimation of cardiac conduction properties from electroanatomical recordings. Medical image analysis. 2014;18(1):228–40. doi: 10.1016/j.media.2013.10.006 pmid:24247034.
  26. 26. Kuijpers NH, Hermeling E, Bovendeerd PH, Delhaas T, Prinzen FW. Modeling cardiac electromechanics and mechanoelectrical coupling in dyssynchronous and failing hearts: insight from adaptive computer models. Journal of cardiovascular translational research. 2012;5(2):159–69. doi: 10.1007/s12265-012-9346-y pmid:22271009; PubMed Central PMCID: PMC3294221.
  27. 27. Niederer SA, Plank G, Chinchapatnam P, Ginks M, Lamata P, Rhode KS, et al. Length-dependent tension in the failing heart and the efficacy of cardiac resynchronization therapy. Cardiovascular research. 2011;89(2):336–43. doi: 10.1093/cvr/cvq318 pmid:20952413.
  28. 28. Sermesant M, Peyrat JM, Chinchapatnam P, Billet F, Mansi T, Rhode K, et al. Toward patient-specific myocardial models of the heart. Heart failure clinics. 2008;4(3):289–301. doi: 10.1016/j.hfc.2008.02.014 pmid:18598981.
  29. 29. Krishnamurthy A, Villongco CT, Chuang J, Frank LR, Nigam V, Belezzuoli E, et al. Patient-Specific Models of Cardiac Biomechanics. Journal of computational physics. 2013;244:4–21. doi: 10.1016/j.jcp.2012.09.015 pmid:23729839; PubMed Central PMCID: PMC3667962.
  30. 30. Nielsen PM, Le Grice IJ, Smaill BH, Hunter PJ. Mathematical model of geometry and fibrous structure of the heart. The American journal of physiology. 1991;260(4 Pt 2):H1365–78. pmid:2012234.
  31. 31. Neumann D, M T, Grbic S, Voigt I, Georgescu B, Kayvanpour E, Amr A, Sedaghat-Hamedani F, Haas J, Katus HA, Meder B, Hornegger J, Kamen A, Comaniciu D. Automatic image-to-model framework for patient-specific electromechanical modeling of the heart. Biomedical Imaging (ISBI), 2014 IEEE 11th International Symposium 2014. p. pp. 935–8.
  32. 32. Zheng Y, Barbu A, Georgescu B, Scheuering M, Comaniciu D. Four-chamber heart modeling and automatic segmentation for 3-D cardiac CT volumes using marginal space learning and steerable features. IEEE transactions on medical imaging. 2008;27(11):1668–81. doi: 10.1109/TMI.2008.2004421 pmid:18955181.
  33. 33. Zettinig O, M T, Georgescu B, Rapaka S, Kamen A, Haas J, Karen S.F, Sedaghat-Hamedani F, Kayvanpour E, Amr A, Hardt S, Mereles D, Steen H, Keller A, Katus HA, Meder B, Navab N, Comaniciu D. From medical images to fast computational models of heart electromechanics: an integrated framework towards clinical use. Functional Imaging and Modeling of the Heart. 2013:pp. 249–58. Springer Berlin Heidelberg.
  34. 34. Guetter Ch H X, Chefd'hotel C, Guehring J. Efficient symmetric and inverse-consistent deformable registration through interleaved optimization in Biomedical Imaging: From Nano to Macro. IEEE International Symposium 2011. p. 590–3.
  35. 35. Mitchell CC S D. A two-current model for the dynamics of cardiac membrane. Bulletin of mathematical biology. 2003:767–93. pmid:12909250
  36. 36. Ten Tusscher KH, Noble D, Noble PJ, Panfilov AV. A model for human ventricular tissue. American journal of physiology Heart and circulatory physiology. 2004;286(4):H1573–89. doi: 10.1152/ajpheart.00794.2003 pmid:14656705.
  37. 37. Rapaka S, Mansi T, Georgescu B, Pop M, Wright GA, Kamen A, et al. LBM-EP: Lattice-Boltzmann method for fast cardiac electrophysiology simulation from 3D images. Medical image computing and computer-assisted intervention: MICCAI International Conference on Medical Image Computing and Computer-Assisted Intervention. 2012;15(Pt 2):33–40. pmid:23286029.
  38. 38. Georgescu B RS, Mansi T, Zettinig O, Kamen A, Comaniciu D. Towards real-time cardiac electrophysiology computations using gp-gpu lattice-boltzmann method. High-Performance Computing, a 2013 MICCAI Workshop2013.
  39. 39. Seegerer P, Mansi T, Jolly M-P, Neumann D, Georgescu B, Kamen A, et al. Estimation of Regional Electrical Properties of the Heart from 12-Lead ECG and Images. Statistical Atlases and Computational Models of the Heart-Imaging and Modelling Challenges: Springer; 2015. p. 204–12.
  40. 40. Powell MJ. The NEWUOA software for unconstrained optimization without derivatives. Large-scale nonlinear optimization: Springer; 2006. p. 255–97.
  41. 41. Comas O T Z, Allard J, Ourselin S, Cotin S, Passenger J. Efficient nonlinear FEM for soft tissue modelling and its GPU implementation within the open source framework SOFA. Biomedical Simulation, Springer Berlin Heidelberg. 2008:pp. 28–39.
  42. 42. Sermesant A D H, Ayache N. An electromechanical model of the heart for image analysis and simulation. IEEE transactions on medical imaging. 2006;25(5):612–25. doi: 10.1109/Tmi.2006.872746. WOS:000237214000009. pmid:16689265
  43. 43. Mansi T. Image-based physiological and statistical models of the heart: Application to tetralogy of fallot. 2010.
  44. 44. Segers P, Rietzschel ER, De Buyzere ML, Stergiopulos N, Westerhof N, Van Bortel LM, et al. Three- and four-element Windkessel models: assessment of their fitting performance in a large cohort of healthy middle-aged individuals. Proceedings of the Institution of Mechanical Engineers Part H, Journal of engineering in medicine. 2008;222(4):417–28. pmid:18595354.
  45. 45. Allard J C S, Faure F, Bensoussan PJ, Poyer F, Duriez Ch, Delingette H, Grisoni L. Sofa-an open source framework for medical simulation. In Medicine Meets Virtual Reality, MMVR 15. 2007.
  46. 46. Konukoglu E, Relan J, Cilingir U, Menze BH, Chinchapatnam P, Jadidi A, et al. Efficient probabilistic model personalization integrating uncertainty on data and parameters: Application to eikonal-diffusion models in cardiac electrophysiology. Progress in biophysics and molecular biology. 2011;107(1):134–46. doi: 10.1016/j.pbiomolbio.2011.07.002 pmid:21763715.
  47. 47. Cootes TF T C, Cooper DH, Graha J. Active Shape Models-Their Training and Application. Comp Vis Image Unders. 1995;61(1):39–59.
  48. 48. Levy WC, Mozaffarian D, Linker DT, Sutradhar SC, Anker SD, Cropp AB, et al. The Seattle Heart Failure Model: prediction of survival in heart failure. Circulation. 2006;113(11):1424–33. pmid:16534009.
  49. 49. Lecoq G, Leclercq C, Leray E, Crocq C, Alonso C, de Place C, et al. Clinical and electrocardiographic predictors of a positive response to cardiac resynchronization therapy in advanced heart failure. European heart journal. 2005;26(11):1094–100. doi: 10.1093/eurheartj/ehi146 pmid:15728648.
  50. 50. Mollema SA, Bleeker GB, van der Wall EE, Schalij MJ, Bax JJ. Usefulness of QRS duration to predict response to cardiac resynchronization therapy in patients with end-stage heart failure. The American journal of cardiology. 2007;100(11):1665–70. doi: 10.1016/j.amjcard.2007.06.071 pmid:18036366.
  51. 51. Dye C, Boerma T., Evans D., Harries A., Lienhardt Ch., McManus J., Pang T., Terry R., Zachariah R. Research for Universal Health Coverage 2013.
  52. 52. Zhou L, Solhjoo S, Millare B, Plank G, Abraham MR, Cortassa S, et al. Effects of regional mitochondrial depolarization on electrical propagation: implications for arrhythmogenesis. Circulation Arrhythmia and electrophysiology. 2014;7(1):143–51. doi: 10.1161/CIRCEP.113.000600 pmid:24382411; PubMed Central PMCID: PMC4001739.
  53. 53. Marchesseau S, Delingette H, Sermesant M, Cabrera-Lozoya R, Tobon-Gomez C, Moireau P, et al. Personalization of a cardiac electromechanical model using reduced order unscented Kalman filtering from regional volumes. Medical image analysis. 2013;17(7):816–29. doi: 10.1016/j.media.2013.04.012 pmid:23707227.
  54. 54. Neumann D, Mansi T, Georgescu B, Kamen A, Kayvanpour E, Amr A, et al. Robust image-based estimation of cardiac tissue parameters and their uncertainty from noisy data. Medical image computing and computer-assisted intervention: MICCAI International Conference on Medical Image Computing and Computer-Assisted Intervention. 2014;17(Pt 2):9–16. pmid:25485357.
  55. 55. Boulakia M C S, Fernández MA, Gerbeau JF, Zemzemi N Mathematical modeling of electrocardiograms: a numerical study. Annals of biomedical engineering. 2010;38(3):1071–97. doi: 10.1007/s10439-009-9873-0. pmid:20033779
  56. 56. Holzapfel GA, Ogden RW. Constitutive modelling of passive myocardium: a structurally based framework for material characterization. Philosophical transactions Series A, Mathematical, physical, and engineering sciences. 2009;367(1902):3445–75. doi: 10.1098/rsta.2009.0091 pmid:19657007.