Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Carrick, Richard T., Bates, Oliver R. J., Benson, Bryce E., Habel, Nicole, Bates, Jason H. T., Spector, Peter S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
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
_version_ 1782361326619721728
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
work_keys_str_mv AT carrickrichardt prospectivelyquantifyingthepropensityforatrialfibrillationamechanisticformulation
AT batesoliverrj prospectivelyquantifyingthepropensityforatrialfibrillationamechanisticformulation
AT bensonbrycee prospectivelyquantifyingthepropensityforatrialfibrillationamechanisticformulation
AT habelnicole prospectivelyquantifyingthepropensityforatrialfibrillationamechanisticformulation
AT batesjasonht prospectivelyquantifyingthepropensityforatrialfibrillationamechanisticformulation
AT spectorpeters prospectivelyquantifyingthepropensityforatrialfibrillationamechanisticformulation