Evidence map›Paper›PMID 32607500›Full record

ArticlePhysical review research

Understanding the transition from paroxysmal to persistent atrial fibrillation.

Alberto Ciacci, Max Falkenberg, Kishan A Manani, Tim S Evans, Nicholas S Peters, Kim Christensen

Open access · goldAbstract read
In one paragraph

Article in Physical review research. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact, top 100% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 0 citations in OpenAlex.

  1. Gut microbiota and atrial cardiomyopathy.Frontiers in cardiovascular medicine · 2025
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Alberto Ciacci *Blackett Laboratory, Imperial College London, London SW7 2BW, United Kingdom.ORCID https://orcid.org/0000-0002-1514-2162
Max Falkenberg *Blackett Laboratory, Imperial College London, London SW7 2BW, United Kingdom.ORCID https://orcid.org/0000-0002-2986-2494
Kishan A MananiBlackett Laboratory, Imperial College London, London SW7 2BW, United Kingdom.
Tim S EvansBlackett Laboratory, Imperial College London, London SW7 2BW, United Kingdom.ORCID https://orcid.org/0000-0003-3501-6486
Nicholas S PetersElectroCardioMaths Programme, Imperial Centre for Cardiac Engineering, Imperial College London, London W12 0NN, United Kingdom.ORCID https://orcid.org/0000-0002-3581-8078
Kim ChristensenBlackett Laboratory, Imperial College London, London SW7 2BW, United Kingdom.ORCID https://orcid.org/0000-0002-7648-7332
Imperial College London · GB

Funding

British Heart Foundation RE/18/4/34215British Heart Foundation RG/16/3/32175
6 · The paper itself

Abstract

Atrial fibrillation (AF) is the most common cardiac arrhytmia, characterized by the chaotic motion of electrical wavefronts in the atria. In clinical practice, AF is classified under two primary categories: paroxysmal AF, short intermittent episodes separated by periods of normal electrical activity; and persistent AF, longer uninterrupted episodes of chaotic electrical activity. However, the precise reasons why AF in a given patient is paroxysmal or persistent is poorly understood. Recently, we have introduced the percolation-based Christensen-Manani-Peters (CMP) model of AF which naturally exhibits both paroxysmal and persistent AF, but precisely how these differences emerge in the model is unclear. In this paper, we dissect the CMP model to identify the cause of these different AF classifications. Starting from a mean-field model where we describe AF as a simple birth-death process, we add layers of complexity to the model and show that persistent AF arises from reentrant circuits which exhibit an asymmetry in their probability of activation relative to deactivation. As a result, different simulations generated at identical model parameters can exhibit fibrillatory episodes spanning several orders of magnitude from a few seconds to months. These findings demonstrate that diverse, complex fibrillatory dynamics can emerge from very simple dynamics in models of AF.

Identifiers

PMID32607500
PMCPMC7326608
OpenAlexW2964760860

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.