Evidence map›Paper›PMID 31899215›Full record

ArticleProgress in biophysics and molecular biology2020

Temporal irregularity quantification and mapping of optical action potentials using wave morphology similarity.

Christopher O'Shea, James Winter, Andrew P Holmes, Daniel M Johnson, Joao N Correia, Paulus Kirchhof, Larissa Fabritz, Kashif Rajpoot, Davor Pavlovic

Open access · hybridAbstract read
In one paragraph

Article in Progress in biophysics and molecular biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 23% 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

5 citing papers in PubMed, 5 citations in OpenAlex.

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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

9 authors at 3 institutions in 1 country.

Christopher O'SheaInstitute of Cardiovascular Sciences, University of Birmingham, UK; EPSRC Centre for Doctoral Training in Physical Sciences for Health, School of Chemistry, University of Birmingham, UK; School of Computer Science, University of Birmingham, Birmingham, B15 2TT, UK.
James WinterInstitute of Cardiovascular Sciences, University of Birmingham, UK.
Andrew P HolmesInstitute of Cardiovascular Sciences, University of Birmingham, UK; Institute of Clinical Sciences, University of Birmingham, UK.
Daniel M JohnsonInstitute of Cardiovascular Sciences, University of Birmingham, UK.
Joao N CorreiaInstitute of Microbiology and Infection, School of Biosciences, University of Birmingham, UK.
Paulus KirchhofInstitute of Cardiovascular Sciences, University of Birmingham, UK; Department of Cardiology, UHB NHS Foundation Trust, Birmingham, UK; Cardiology Specialty, SWBH NHS Trust, Birmingham, UK.
Larissa FabritzInstitute of Cardiovascular Sciences, University of Birmingham, UK; Department of Cardiology, UHB NHS Foundation Trust, Birmingham, UK.
Kashif RajpootSchool of Computer Science, University of Birmingham, Birmingham, B15 2TT, UK. Electronic address: k.m.rajpoot@bham.ac.uk.
Davor PavlovicInstitute of Cardiovascular Sciences, University of Birmingham, UK. Electronic address: d.pavlovic@bham.ac.uk.
University of Birmingham · GBUniversity Hospitals Bristol and Weston NHS Foundation TrustEngineering and Physical Sciences Research Council · GB

Funding

British Heart Foundation AA/18/2/34218British Heart Foundation FS/13/43/30324British Heart Foundation FS/16/35/31952British Heart Foundation FS/19/12/34204British Heart Foundation FS/19/16/34169British Heart Foundation PG/17/30/32961British Heart Foundation PG/17/55/33087British Heart Foundation RG/17/15/33106Wellcome Trust 109604/Z/15/Z
6 · The paper itself

Abstract

backgroundCardiac optical mapping enables direct and high spatio-temporal resolution recording of action potential (AP) morphology. Temporal alterations in AP morphology are both predictive and consequent of arrhythmia. Here we sought to test if methods that quantify regularity of recorded waveforms could be applied to detect and quantify periods of temporal instability in optical mapping datasets in a semi-automated, user-unbiased manner. METHODS AND

resultsWe developed, tested and applied algorithms to quantify optical wave similarity (OWS) to study morphological temporal similarity of optically recorded APs. Unlike other measures (e.g. alternans ratio, beat-to-beat variability, arrhythmia scoring), the quantification of OWS is achieved without a restrictive definition of specific signal points/features and is instead derived by analysing the complete morphology from the entire AP waveform. Using model datasets, we validated the ability of OWS to measure changes in AP morphology, and tested OWS mapping in guinea pig hearts and mouse atria. OWS successfully detected and measured alterations in temporal regularity in response to several proarrhythmic stimuli, including alterations in pacing frequency, premature contractions, alternans and ventricular fibrillation.

conclusionOWS mapping provides an effective measure of temporal regularity that can be applied to optical datasets to detect and quantify temporal alterations in action potential morphology. This methodology provides a new metric for arrhythmia inducibility and scoring in optical mapping datasets.

Indexed as

Action PotentialsAlgorithmsAnimalsArrhythmias, CardiacGuinea PigsHeartHeart AtriaMiceNormal DistributionOptics and PhotonicsTime FactorsVentricular FibrillationOptical action potentialOptical mappingRegularity indexTemporal stabilityWave similarity

Identifiers

PMID31899215
PMCPMC7607254
OpenAlexW2998546254

What OpenQuestion holds

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LicenceCC BY
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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.