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Prospectively Quantifying the Propensity for Atrial Fibrillation: A Mechanistic Formulation
The goal of this study was to determine quantitative relationships between electrophysiologic parameters and the propensity of cardiac tissue to undergo atrial fibrillation. We used a computational model to simulate episodes of fibrillation, which we then characterized in terms of both their duratio...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4358999/ https://www.ncbi.nlm.nih.gov/pubmed/25768978 http://dx.doi.org/10.1371/journal.pone.0118746 |
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author | Carrick, Richard T. Bates, Oliver R. J. Benson, Bryce E. Habel, Nicole Bates, Jason H. T. Spector, Peter S. |
author_facet | Carrick, Richard T. Bates, Oliver R. J. Benson, Bryce E. Habel, Nicole Bates, Jason H. T. Spector, Peter S. |
author_sort | Carrick, Richard T. |
collection | PubMed |
description | The goal of this study was to determine quantitative relationships between electrophysiologic parameters and the propensity of cardiac tissue to undergo atrial fibrillation. We used a computational model to simulate episodes of fibrillation, which we then characterized in terms of both their duration and the population dynamics of the electrical waves which drove them. Monte Carlo sampling revealed that episode durations followed an exponential decay distribution and wave population sizes followed a normal distribution. Half-lives of reentrant episodes increased exponentially with either increasing tissue area to boundary length ratio (A/BL) or decreasing action potential duration (APD), resistance (R) or capacitance (C). We found that the qualitative form of fibrillatory activity (e.g., multi-wavelet reentry (MWR) vs. rotors) was dependent on the ratio of resistance and capacitance to APD; MWR was reliably produced below a ratio of 0.18. We found that a composite of these electrophysiologic parameters, which we term the fibrillogenicity index (Fb = A/(BL*APD*R*C)), reliably predicted the duration of MWR episodes (r(2) = 0.93). Given that some of the quantities comprising Fb are amenable to manipulation (via either pharmacologic treatment or catheter ablation), these findings provide a theoretical basis for the development of titrated therapies of atrial fibrillation. |
format | Online Article Text |
id | pubmed-4358999 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-43589992015-03-23 Prospectively Quantifying the Propensity for Atrial Fibrillation: A Mechanistic Formulation Carrick, Richard T. Bates, Oliver R. J. Benson, Bryce E. Habel, Nicole Bates, Jason H. T. Spector, Peter S. PLoS One Research Article The goal of this study was to determine quantitative relationships between electrophysiologic parameters and the propensity of cardiac tissue to undergo atrial fibrillation. We used a computational model to simulate episodes of fibrillation, which we then characterized in terms of both their duration and the population dynamics of the electrical waves which drove them. Monte Carlo sampling revealed that episode durations followed an exponential decay distribution and wave population sizes followed a normal distribution. Half-lives of reentrant episodes increased exponentially with either increasing tissue area to boundary length ratio (A/BL) or decreasing action potential duration (APD), resistance (R) or capacitance (C). We found that the qualitative form of fibrillatory activity (e.g., multi-wavelet reentry (MWR) vs. rotors) was dependent on the ratio of resistance and capacitance to APD; MWR was reliably produced below a ratio of 0.18. We found that a composite of these electrophysiologic parameters, which we term the fibrillogenicity index (Fb = A/(BL*APD*R*C)), reliably predicted the duration of MWR episodes (r(2) = 0.93). Given that some of the quantities comprising Fb are amenable to manipulation (via either pharmacologic treatment or catheter ablation), these findings provide a theoretical basis for the development of titrated therapies of atrial fibrillation. Public Library of Science 2015-03-13 /pmc/articles/PMC4358999/ /pubmed/25768978 http://dx.doi.org/10.1371/journal.pone.0118746 Text en © 2015 Carrick et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Carrick, Richard T. Bates, Oliver R. J. Benson, Bryce E. Habel, Nicole Bates, Jason H. T. Spector, Peter S. Prospectively Quantifying the Propensity for Atrial Fibrillation: A Mechanistic Formulation |
title | Prospectively Quantifying the Propensity for Atrial Fibrillation: A Mechanistic Formulation |
title_full | Prospectively Quantifying the Propensity for Atrial Fibrillation: A Mechanistic Formulation |
title_fullStr | Prospectively Quantifying the Propensity for Atrial Fibrillation: A Mechanistic Formulation |
title_full_unstemmed | Prospectively Quantifying the Propensity for Atrial Fibrillation: A Mechanistic Formulation |
title_short | Prospectively Quantifying the Propensity for Atrial Fibrillation: A Mechanistic Formulation |
title_sort | prospectively quantifying the propensity for atrial fibrillation: a mechanistic formulation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4358999/ https://www.ncbi.nlm.nih.gov/pubmed/25768978 http://dx.doi.org/10.1371/journal.pone.0118746 |
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