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Absence of Rapid Propagation through the Purkinje Network as a Potential Cause of Line Block in the Human Heart with Left Bundle Branch Block

Background: Cardiac resynchronization therapy is an effective device therapy for heart failure patients with conduction block. However, a problem with this invasive technique is the nearly 30% of non-responders. A number of studies have reported a functional line of block of cardiac excitation propa...

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Autores principales: Okada, Jun-ichi, Washio, Takumi, Nakagawa, Machiko, Watanabe, Masahiro, Kadooka, Yoshimasa, Kariya, Taro, Yamashita, Hiroshi, Yamada, Yoko, Momomura, Shin-ichi, Nagai, Ryozo, Hisada, Toshiaki, Sugiura, Seiryo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5808183/
https://www.ncbi.nlm.nih.gov/pubmed/29467667
http://dx.doi.org/10.3389/fphys.2018.00056
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author Okada, Jun-ichi
Washio, Takumi
Nakagawa, Machiko
Watanabe, Masahiro
Kadooka, Yoshimasa
Kariya, Taro
Yamashita, Hiroshi
Yamada, Yoko
Momomura, Shin-ichi
Nagai, Ryozo
Hisada, Toshiaki
Sugiura, Seiryo
author_facet Okada, Jun-ichi
Washio, Takumi
Nakagawa, Machiko
Watanabe, Masahiro
Kadooka, Yoshimasa
Kariya, Taro
Yamashita, Hiroshi
Yamada, Yoko
Momomura, Shin-ichi
Nagai, Ryozo
Hisada, Toshiaki
Sugiura, Seiryo
author_sort Okada, Jun-ichi
collection PubMed
description Background: Cardiac resynchronization therapy is an effective device therapy for heart failure patients with conduction block. However, a problem with this invasive technique is the nearly 30% of non-responders. A number of studies have reported a functional line of block of cardiac excitation propagation in responders. However, this can only be detected using non-contact endocardial mapping. Further, although the line of block is considered a sign of responders to therapy, the mechanism remains unclear. Methods: Herein, we created two patient-specific heart models with conduction block and simulated the propagation of excitation based on a cellmodel of electrophysiology. In one model with a relatively narrow QRS width (176 ms), we modeled the Purkinje network using a thin endocardial layer with rapid conduction. To reproduce a wider QRS complex (200 ms) in the second model, we eliminated the Purkinje network, and we simulated the endocardial mapping by solving the inverse problem according to the actual mapping system. Results: We successfully observed the line of block using non-contact mapping in the model without the rapid propagation of excitation through the Purkinje network, although the excitation in the wall propagated smoothly. This model of slow conduction also reproduced the characteristic properties of the line of block, including dense isochronal lines and fractionated local electrocardiograms. Further, simulation of ventricular pacing from the lateral wall shifted the location of the line of block. By contrast, in the model with the Purkinje network, propagation of excitation in the endocardial map faithfully followed the actual propagation in the wall, without showing the line of block. Finally, switching the mode of propagation between the two models completely reversed these findings. Conclusions: Our simulation data suggest that the absence of rapid propagation of excitation through the Purkinje network is the major cause of the functional line of block recorded by non-contact endocardial mapping. The line of block can be used to identify responders as these patients loose rapid propagation through the Purkinje network.
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spelling pubmed-58081832018-02-21 Absence of Rapid Propagation through the Purkinje Network as a Potential Cause of Line Block in the Human Heart with Left Bundle Branch Block Okada, Jun-ichi Washio, Takumi Nakagawa, Machiko Watanabe, Masahiro Kadooka, Yoshimasa Kariya, Taro Yamashita, Hiroshi Yamada, Yoko Momomura, Shin-ichi Nagai, Ryozo Hisada, Toshiaki Sugiura, Seiryo Front Physiol Physiology Background: Cardiac resynchronization therapy is an effective device therapy for heart failure patients with conduction block. However, a problem with this invasive technique is the nearly 30% of non-responders. A number of studies have reported a functional line of block of cardiac excitation propagation in responders. However, this can only be detected using non-contact endocardial mapping. Further, although the line of block is considered a sign of responders to therapy, the mechanism remains unclear. Methods: Herein, we created two patient-specific heart models with conduction block and simulated the propagation of excitation based on a cellmodel of electrophysiology. In one model with a relatively narrow QRS width (176 ms), we modeled the Purkinje network using a thin endocardial layer with rapid conduction. To reproduce a wider QRS complex (200 ms) in the second model, we eliminated the Purkinje network, and we simulated the endocardial mapping by solving the inverse problem according to the actual mapping system. Results: We successfully observed the line of block using non-contact mapping in the model without the rapid propagation of excitation through the Purkinje network, although the excitation in the wall propagated smoothly. This model of slow conduction also reproduced the characteristic properties of the line of block, including dense isochronal lines and fractionated local electrocardiograms. Further, simulation of ventricular pacing from the lateral wall shifted the location of the line of block. By contrast, in the model with the Purkinje network, propagation of excitation in the endocardial map faithfully followed the actual propagation in the wall, without showing the line of block. Finally, switching the mode of propagation between the two models completely reversed these findings. Conclusions: Our simulation data suggest that the absence of rapid propagation of excitation through the Purkinje network is the major cause of the functional line of block recorded by non-contact endocardial mapping. The line of block can be used to identify responders as these patients loose rapid propagation through the Purkinje network. Frontiers Media S.A. 2018-02-06 /pmc/articles/PMC5808183/ /pubmed/29467667 http://dx.doi.org/10.3389/fphys.2018.00056 Text en Copyright © 2018 Okada, Washio, Nakagawa, Watanabe, Kadooka, Kariya, Yamashita, Yamada, Momomura, Nagai, Hisada and Sugiura. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Okada, Jun-ichi
Washio, Takumi
Nakagawa, Machiko
Watanabe, Masahiro
Kadooka, Yoshimasa
Kariya, Taro
Yamashita, Hiroshi
Yamada, Yoko
Momomura, Shin-ichi
Nagai, Ryozo
Hisada, Toshiaki
Sugiura, Seiryo
Absence of Rapid Propagation through the Purkinje Network as a Potential Cause of Line Block in the Human Heart with Left Bundle Branch Block
title Absence of Rapid Propagation through the Purkinje Network as a Potential Cause of Line Block in the Human Heart with Left Bundle Branch Block
title_full Absence of Rapid Propagation through the Purkinje Network as a Potential Cause of Line Block in the Human Heart with Left Bundle Branch Block
title_fullStr Absence of Rapid Propagation through the Purkinje Network as a Potential Cause of Line Block in the Human Heart with Left Bundle Branch Block
title_full_unstemmed Absence of Rapid Propagation through the Purkinje Network as a Potential Cause of Line Block in the Human Heart with Left Bundle Branch Block
title_short Absence of Rapid Propagation through the Purkinje Network as a Potential Cause of Line Block in the Human Heart with Left Bundle Branch Block
title_sort absence of rapid propagation through the purkinje network as a potential cause of line block in the human heart with left bundle branch block
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5808183/
https://www.ncbi.nlm.nih.gov/pubmed/29467667
http://dx.doi.org/10.3389/fphys.2018.00056
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