D U J Keller

Karlsruhe Institute of Technology, Carlsruhe, Baden-Württemberg, Germany

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Publications (44)21.09 Total impact

  • Source
    G Seemann · M Alvarez de Eulate · O Dössel · D U J Keller ·

    Biomedizinische Technik/Biomedical Engineering 09/2013; DOI:10.1515/bmt-2013-4319 · 1.46 Impact Factor
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    ABSTRACT: Atrial fibrillation (AF) is the most common cardiac arrhythmia, and the total number of AF patients is constantly increasing. The mechanisms leading to and sustaining AF are not completely understood yet. Heterogeneities in atrial electrophysiology seem to play an important role in this context. Although some heterogeneities have been used in in-silico human atrial modeling studies, they have not been thoroughly investigated. In this study, the original electrophysiological (EP) models of Courtemanche et al., Nygren et al. and Maleckar et al. were adjusted to reproduce action potentials in 13 atrial regions. The parameter sets were validated against experimental action potential duration data and ECG data from patients with AV block. The use of the heterogeneous EP model led to a more synchronized repolarization sequence in a variety of 3D atrial anatomical models. Combination of the heterogeneous EP model with a model of persistent AF-remodeled electrophysiology led to a drastic change in cell electrophysiology. Simulated Ta-waves were significantly shorter under the remodeling. The heterogeneities in cell electrophysiology explain the previously observed Ta-wave effects. The results mark an important step toward the reliable simulation of the atrial repolarization sequence, give a deeper understanding of the mechanism of atrial repolarization and enable further clinical investigations.
    Medical & Biological Engineering 07/2013; 51(10). DOI:10.1007/s11517-013-1090-1 · 1.73 Impact Factor
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    ABSTRACT: Multiscale cardiac modeling has made great advances over the last decade. Highly detailed atrial models were created and used for the investigation of initiation and perpetuation of atrial fibrillation. The next challenge is the use of personalized atrial models in clinical practice. In this study, a framework of simple and robust tools is presented, which enables the generation and validation of patient-specific anatomical and electrophysiological atrial models. Introduction of rule-based atrial fiber orientation produced a realistic excitation sequence and a better correlation to the measured electrocardiograms. Personalization of the global conduction velocity lead to a precise match of the measured P-wave duration. The use of a virtual cohort of nine patient and volunteer models averaged out possible model-specific errors. Intra-atrial excitation conduction was personalized manually from left atrial local activation time maps. Inclusion of LE-MRI data into the simulations revealed possible gaps in ablation lesions. A fast marching level set approach to compute atrial depolarization was extended to incorporate anisotropy and conduction velocity heterogeneities and reproduced the monodomain solution. The presented chain of tools is an important step towards the use of atrial models for the patient-specific AF diagnosis and ablation therapy planing.
    IEEE Transactions on Medical Imaging 01/2013; 32(1):73-84. DOI:10.1109/TMI.2012.2201948 · 3.39 Impact Factor
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    ABSTRACT: Congenital Long-QT Syndrome (LQTS) is a genetic disorder affecting the repolarization of the heart. The most prevalent subtypes of LQTS are LQT1-3. In this work, we aim to evaluate the differences in the T-waves of simulated LQT1-3 in order to identify markers in the ECG that might help to classify patients solely based on ECG measurements. For LQT1, mutation S277L was used to characterize IKs and mutation S818L in IKr for LQT2. Voltage clamp data were used to parametrize the ion channel equations of the ten Tusscher and Panfilov model of human ventricular electrophysiology. LQT3 was integrated using an existing mutant INa model. The monodomain model was used in a transmural and apico-basal heterogeneous model of the ventricles to calculate ventricular excitation propagation. The forward calculation on a torso model was performed to determine body surface ECGs. Compared to the physiological case with a QT-time of 375 ms, this interval was prolonged in all LQTS (LQT1 423 ms; LQT2 394 ms; LQT3 405 ms). The T-wave amplitude was changed (Einthoven lead II: LQT1 108%; LQT2 91%; LQT3 103%). Also, the width of the T-wave was enlarged (full width at half maximum: LQT1 111%; LQT2 125%; LQT3 109%). At the current state of modeling and data analysis, the three LQTS have not been distinguishable solely by ECG data.
    Computing in Cardiology Conference (CinC), 2013; 01/2013
  • David U. J. Keller · Daniel L. Weiß · Olaf Dössel · Gunnar Seemann ·

  • David U J Keller · Daniel L Weiss · Olaf Dossel · Gunnar Seemann ·
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    ABSTRACT: Despite the commonly accepted notion that action potential duration (APD) is distributed heterogeneously throughout the ventricles and that the associated dispersion of repolarization is mainly responsible for the shape of the T-wave, its concordance and exact morphology are still not completely understood. This paper evaluated the T-waves for different previously measured heterogeneous ion channel distributions. To this end, cardiac activation and repolarization was simulated on a high resolution and anisotropic biventricular model of a volunteer. From the same volunteer, multichannel ECG data were obtained. Resulting transmembrane voltage distributions for the previously measured heterogeneous ion channel expressions were used to calculate the ECG and the simulated T-wave was compared to the measured ECG for quantitative evaluation. Both exclusively transmural (TM) and exclusively apico-basal (AB) setups produced concordant T-waves, whereas interventricular (IV) heterogeneities led to notched T-wave morphologies. The best match with the measured T-wave was achieved for a purely AB setup with shorter apical APD and a mix of AB and TM heterogeneity with M-cells in midmyocardial position and shorter apical APD. Finally, we probed two configurations in which the APD was negatively correlated with the activation time. In one case, this meant that the repolarization directly followed the sequence of activation. Still, the associated T-waves were concordant albeit of low amplitude.
    IEEE transactions on bio-medical engineering 09/2011; 59(2):311-22. DOI:10.1109/TBME.2011.2168397 · 2.35 Impact Factor
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    ABSTRACT: Ventricular wall deformation is widely assumed to have an impact on the morphology of the T-wave that can be measured on the body surface. This study aims at quantifying these effects based on an in silico approach. To this end, we used a hybrid, static-dynamic approach: action potential propagation and repolarization were simulated on an electrophysiologically detailed but static 3-D heart model while the forward calculation accounted for ventricular deformation and the associated movement of the electrical sources (thus, it was dynamic). The displacement vectors that describe the ventricular motion were extracted from cinematographic and tagged MRI data using an elastic registration procedure. To probe to what extent the T-wave changes depend on the synchrony/asynchrony of mechanical relaxation and electrical repolarization, we created three electrophysiological configurations, each with a unique QT time: a setup with physiological QT time, a setup with pathologically short QT time (SQT), and pathologically long QT time (LQT), respectively. For all three electrophysiological configurations, a reduction of the T-wave amplitude was observed when the dynamic model was used for the forward calculations. The largest amplitude changes and the lowest correlation coefficients between the static and dynamic model were observed for the SQT setup, followed by the physiological QT and LQT setups.
    IEEE transactions on bio-medical engineering 07/2011; 58(7):2109-19. DOI:10.1109/TBME.2011.2147785 · 2.35 Impact Factor
  • T. Fritz · O. Jarrousse · D. U. J. Keller · G. Seemann · O. Dössel ·
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    ABSTRACT: The impact of transmural infarctions of the left ventricle on the cardiac mechanical dynamics is evaluated for all 17 AHA segments in a computer model. The simulation framework consists of two parts: an electrophysiological model and an elastomechanical model of the ventricles. The electrophysiological model is used to simulate the electrophysiological processes on cellular level, excitation propagation and the tension development. It is linked to the elastomechanical model, which is based on nonlinear finite element analysis for continuum mechanics. Altogether, 18 simulations of the contraction of the ventricles were performed, 17 with an infarction in the respective AHA segment and one simulation for the control case. For each simulation, the mechanical dynamics as well as the wall thickening of the infarct region were analyzed and compared to the corresponding region of the control case. The simulation revealed details of the impact of the myocardial infarction on wall thickening as well as on the velocity of the infarct region for most of the AHA segments. KeywordsMyocardial Infarction–Heart Modeling–Finite Element Analysis
    05/2011: pages 241-249;
  • T. Fritz · O. Jarrousse · David U. J. Keller · Gunnar Seemann · Olaf Dössel ·

    Functional Imaging and Modeling of the Heart - 6th International Conference, FIMH 2011, New York City, NY, USA, May 25-27, 2011. Proceedings; 01/2011
  • M W Krueger · V Schmidt · F M Weber · D U J Keller · G Seemann · O Dössel ·
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    ABSTRACT: Atrial fibre architecture has complex patterns of bundles and layers and is known to impact on atrial electrophysiology, especially in fast-conducting bundles like Crista Terminalis, Bachmann?s bundle and pectinate muscles. Based on a priori knowledge of atrial fibre structure, we incorporated rule-based fibre orientation in seven volumetric models of human atria using a semi-automatic approach. We were able to introduce multiple layers of myofibres and regional heterogeneities of ion channels in the models. We evaluated the influence of complete atrial fibre architecture on multiple modelling scales. First, we simulated atrial excitation in the isotropic and anisotropic models using the model of Courtemanche et al. in combination with the monodomain approach. Second, we computed body surface potentials from the simulated transmembrane voltages and compared these to measured ECGs from the respective patients. Temporal behaviour of the atrial excitation sequences was significantly altered in the anisotropic models compared to the sequences in the isotropic models. Complete atrial activation was achieved approximately 20% faster in the anisotropic models mostly due to fast conducting myofibre bundles. Electrophysiological heterogeneities influenced right atrial transmembrane voltage distribution over time due to a less negative action potential plateau in Crista Terminalis cells. P-wave duration was significantly shorted by the introduction of atrial anisotropy and the error to measured P-wave duration was reduced. Furthermore, a pattern change in body surface potential distribution over time was observed. The anisotropic patterns showed a better match to the measurements. Thus, the modelling error by using generalised fibre architecture for patient-specific models was smaller than by using isotropic models. The results highlight the necessity to incorporate atrial anisotropy in personalised models to produce more realistic simulations. The semi-automatic approach allows the use of these models for future clinical applications.
    Cardiac Physiome Conference 2011; 01/2011
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    ABSTRACT: Atrial myofiber orientation is complex and has multiple discrete layers and bundles. A novel robust semi-automatic method to incorporate atrial anisotropy and heterogeneities into patient-specific models is introduced. The user needs to provide 22 distinct seed-points from which a network of auxiliary lines is constructed. These are used to define fiber orientation and myocardial bundles. The method was successfully applied to twelve patient-specific volumetric voxel models derived from CT, MRI and photographic data. Initial electrophysiological simulations show a significant influence of anisotropy and heterogeneity on the excitation pattern, P-wave duration (19.9% shortening) and repolarisation behavior. Fiber modeling results show overall good correspondence with anatomical data. Minor modeling errors are observed if more than four pulmonary veins exist in the model. The method is an important step towards the creation of realistic patient-specific atria models for clinical practice.
    Functional Imaging and Modeling of the Heart - 6th International Conference, FIMH 2011, New York City, NY, USA, May 25-27, 2011. Proceedings; 01/2011
  • Source
    D.U.J. Keller · A. Bohn · O. Dössel · G. Seemann ·
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    ABSTRACT: Patients suffering from the congenital Long-QT syndrome have been reported to react highly sensitive to the presence of β-adrenergic agents that are produced by the sympathetic nervous system. In this work we used an anisotropic and electrophysiologically heterogeneous insilico model to reproduce wedge experiments in which the Long-QT syndrome was induced pharmacologically. The integration of an intracellular signaling cascade allowed the prediction of the effects of adrenergic agents on the different subtypes of the Long-QT syndrome. For LQT1 the in-silico model predicted a QT prolongation in the transmural pseudo ECG without an increase in transmural dispersion of repolarization. For LQT2 and LQT3 the QT prolongation was accompanied by an increased transmural dispersion of repolarization. β-adrenergic tonus shortened the QT interval and increased transmural dispersion of repolarization. These findings were consistent with the experimental reports.
    Computing in Cardiology, 2010; 10/2010
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    ABSTRACT: In this paper, we present an efficient method to estimate changes in forward-calculated body surface potential maps (BSPMs) caused by variations in tissue conductivities. For blood, skeletal muscle, lungs, and fat, the influence of conductivity variations was analyzed using the principal component analysis (PCA). For each single tissue, we obtained the first PCA eigenvector from seven sample simulations with conductivities between ±75% of the default value. We showed that this eigenvector was sufficient to estimate the signal over the whole conductivity range of ±75%. By aligning the origins of the different PCA coordinate systems and superimposing the single tissue effects, it was possible to estimate the BSPM for combined conductivity variations in all four tissues. Furthermore, the method can be used to easily calculate confidence intervals for the signal, i.e., the minimal and maximal possible amplitudes for given conductivity uncertainties. In addition to that, it was possible to determine the most probable conductivity values for a given BSPM signal. This was achieved by probing hundreds of different conductivity combinations with a numerical optimization scheme. In conclusion, our method allows to efficiently predict forward-calculated BSPMs over a wide range of conductivity values from few sample simulations.
    IEEE transactions on bio-medical engineering 10/2010; 58(2):265-73. DOI:10.1109/TBME.2010.2090151 · 2.35 Impact Factor
  • David U J Keller · Frank M Weber · Gunnar Seemann · Olaf Dössel ·
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    ABSTRACT: This paper examined the effects that different tissue conductivities had on forward-calculated ECGs. To this end, we ranked the influence of tissues by performing repetitive forward calculations while varying the respective tissue conductivity. The torso model included all major anatomical structures like blood, lungs, fat, anisotropic skeletal muscle, intestine, liver, kidneys, bone, cartilage, and spleen. Cardiac electrical sources were derived from realistic atrial and ventricular simulations. The conductivity rankings were based on one of two methods: First, we considered fixed percental conductivity changes to probe the sensitivity of the ECG regarding conductivity alterations. Second, we set conductivities to the reported minimum and maximum values to evaluate the effects of the existing conductivity uncertainties. The amplitudes of both atrial and ventricular ECGs were most sensitive for blood, skeletal muscle conductivity and anisotropy as well as for heart, fat, and lungs. If signal morphology was considered, fat was more important whereas skeletal muscle was less important. When comparing atria and ventricles, the lungs had a larger effect on the atria yet the heart conductivity had a stronger impact on the ventricles. The effects of conductivity uncertainties were significant. Future studies dealing with electrocardiographic simulations should consider these effects.
    IEEE transactions on bio-medical engineering 07/2010; 57(7):1568-76. DOI:10.1109/TBME.2010.2046485 · 2.35 Impact Factor
  • Source
    S. Bauer · D. Keller · F. M. Weber · P. Tri Dung · G. Seemann · O. Dössel ·
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    ABSTRACT: Potential distributions on the body surface resulting from a given electrical activity of the heart can be simulated by forward calculations. However, variations in tissue conductivities impact decisively on the results.We used Principal Component Analysis (PCA) to identify the effect of an organ’s conductivity on the body surface potentials for both atrial and ventricular signals. Signal changes were described by a mean signal and one pre-dominant variation pattern calculated using the first PCA eigenvector. Knowing this eigenvector the body surface potentials corresponding to any conductivity value could be constructed. The original and reconstructed signals showed a good match based on the analysis of the root mean squared error. Using an interpolation technique, surface potentials were reconstructed for conductivity values that were not part of the initial sample. This allowed for efficiently predicting the impact of tissue conductivities on the body surface potentials for a wide range of conductivity values from few sample simulations.
    01/2010: pages 641-644;
  • D U J Keller · O Dössel · G Seemann ·
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    ABSTRACT: The shape of a simulated excitation wavefront depends on the underlying spatial resolution. The aim of this work is twofold: On the one hand we investigated the dependency of the wavefront on spatial resolution by simulating the excitation spread in three virtual patches of ventricular tissue that have different resolutions. On the other hand we simulate a realistic excitation sequence in an anisotropic and electrophysiologically heterogeneous biventricular model. Our patch experiments with different spatial resolutions demonstrated that resolutions below 0.2 mm led to a deformation of the excitation wavefront to non-elliptical shapes. The biventricular model with 0.2 mm grid size shows realistic excitation spread and conduction velocities. Similar biventricular models in conjunction with a computational representation of the thorax will be used in future to predict the effects of changes on the ion-channel level on the ECG.
    Proceedings BMT 2010, 44. DGBMT Jahrestagung, 3-Länder-Tagung D-A-CH, Rostock; 01/2010
  • M W Krueger · V Schmidt · D U J Keller · T Fritz · G Seemann · O Dössel ·
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    ABSTRACT: Motivation: Anatomical models of the heart can be used to conduct multi-physics simulations. These simulations can aid basic and clinical research and are being translated into clinical practice nowadays.Problem statement: The human myocardium has very complex fiber structure, which has a strong impact on cardiac physiology. To understand and evaluate 3D fiber orientation in volumetric cardiac models, it is often necessary to project these onto printed pictures.Approach: Images of myocardial fibers using color-coded cylinders, color-coded streamlines and anaglyph methods are compared. Results: Streamlines provide a good distinction of myocardial bundles. Cylinders show the most accurate results. Color-coded representations reveal abrupt changes in fiber direction. Anaglyph visualizations give an illusion of depth in 2D prints and can display overlaying bundles. Conclusions: Streamlines are superior in imaging global fiber orientation, whereas cylinders give better results for local structures. Color-coding increases information where fiber structure is very complex, e.g. in the atria. Anaglyph images cause a loss in color information but help the viewer to understand the 3D object. Overall, it is necessary to choose the appropriate method of picturing fibers for specific tasks.
    KIT PhD Symposium 2010; 01/2010
  • MW Krueger · K Rhode · FM Weber · D U J Keller · D Caulfield · G Seemann · B R Knowles · R Razavi · O Dössel ·
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    ABSTRACT: Current models of the human atria represent geometries of single individuals or base on statistical data. We present a work-flow for the creation of patient-specific atrial models. Furthermore we show a framework to compare simulated P- waves and body surface potential maps (BSPMs) of individual patients with measurements. Models of the atrial and thorax anatomy were segmented from MRI data. Volumetric atrial models were semi-automatically enhanced with electrophys- iologically (EP) relevant structures. Simulations were performed on an anisotropic voxel-based mesh and were forward calculated to obtain simulated BSPMs. BSPMs were acquired using a 64 electrode ECG system. Comparison of simulated and measured P-waves in Einthoven leads showed a general agreement of both, although no personalization of the atrial electrophysiology model was performed. P-wave duration was longer in the simulations, highlighting the need for elec- trophysiological model personalization. Simulated and measured BSPMs revealed similar patterns. The presented method enables realistic simulations of atrial activation on patient-specific volumetric atrial models with EP relevant myocardial structures resulting in computed ECGs (P-wave) and BSPMs with show physiological morphologies
    Biomedizinische Technik / Biomedical Engineering; 01/2010
  • D U J Keller · A Bohn · O Dössel · G Seemann ·
    [Show abstract] [Hide abstract]
    ABSTRACT: Patients suffering from the congenital Long-QT syndrome have been reported to react highly sensitive to the presence of beta-adrenergic agents that are produced by the sympathetic nervous system. In this work we used an anisotropic and electrophysiologically heterogeneous in- silico model to reproduce wedge experiments in which the Long-QT syndrome was induced pharmacologically. The integration of an intracellular signaling cascade allowed the prediction of the effects of adrenergic agents on the different subtypes of the Long-QT syndrome. For LQT1 the in-silico model predicted a QT prolongation in the transmural pseudo ECG without an increase in transmural dispersion of repolarization. For LQT2 and LQT3 the QT prolongation was accompanied by an increased transmural dispersion of repolarization. beta-adrenergic tonus shortened the QT interval and increased transmural dispersion of repolarization. These findings were consistent with the experimental reports.
    Proceedings Computing in Cardiology; 01/2010
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    ABSTRACT: Simulations of the electrophysiological behavior of the heart improve the comprehension of the mechanisms of the cardiovascular system. Furthermore, the mathematical modeling will support diagnosis and therapy of patients suffering from heart diseases. In this paper, the chain of modeling of the electrical function in the heart is described. The components are explained briefly, namely modeling of cardiac geometry, reconstructing the cardiac electrophysiology and excitation propagation. Additionally, the mathematical methods allowing to implement and solve these models are outlined. The three recently more investigated cases atrial fibrillation, ischemia and long-QT syndrome are described and show how cardiac modeling can support cardiologists in answering their open questions.
    it - Information Technology 01/2010; 52(5):242-249. DOI:10.1524/itit.2010.0598

Publication Stats

224 Citations
21.09 Total Impact Points


  • 2007-2013
    • Karlsruhe Institute of Technology
      • Institute of Biomedical Engineering (IBT)
      Carlsruhe, Baden-Württemberg, Germany
  • 2009
    • Institute of Electrical and Electronics Engineers
      Washington, Washington, D.C., United States