Evidence map›Paper›PMID 26701222›Full record

ArticleProgress in biophysics and molecular biology2016

Variability in cardiac electrophysiology: Using experimentally-calibrated populations of models to move beyond the single virtual physiological human paradigm.

Anna Muszkiewicz, Oliver J Britton, Philip Gemmell, Elisa Passini, Carlos Sánchez, Xin Zhou, Annamaria Carusi, T Alexander Quinn, Kevin Burrage, Alfonso Bueno-Orovio and 1 more

Abstract read
In one paragraph

Article in Progress in biophysics and molecular biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 106 papers.

0numbers the graph read from it
0cells of the map it votes in
106citing papers in PubMed
–field-weighted citation impact
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

106 citing papers in PubMed.

  1. A Computational Model of Oxidative Stress in a Human Ventricular Myocyte.bioRxiv : the preprint server for biology · 2026
    Article
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  8. Population Modeling Approach for Human Cardiac Arrhythmia Risk Prediction.Circulation. Arrhythmia and electrophysiology · 2026
    Article
  9. Article
  10. Review
  11. Article
  12. Large-scale synthetic data enable digital twins of human excitable cells.bioRxiv : the preprint server for biology · 2025
    Article
  13. Article
  14. Article
  15. Early Atrial Remodeling Drives Arrhythmia in Fabry Disease.Circulation. Arrhythmia and electrophysiology · 2025
    Article
  16. Article
  17. Frontiers in pharmacology · 2025
    Article
  18. Article
  19. Review
  20. Cell-to-cell heterogeneity in ion channel conductance impacts substrate vulnerability to arrhythmia.American journal of physiology. Heart and circulatory physiology · 2024
    Article

46 more citing papers are in PubMed but not listed here.

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

11 authors.

Anna MuszkiewiczDepartment of Computer Science, University of Oxford, Parks Road, Oxford OX1 3QD, United Kingdom.
Oliver J BrittonDepartment of Computer Science, University of Oxford, Parks Road, Oxford OX1 3QD, United Kingdom.
Philip GemmellClyde Biosciences Ltd, West Medical Building, University of Glasgow, Glasgow G12 8QQ, United Kingdom.
Elisa PassiniDepartment of Computer Science, University of Oxford, Parks Road, Oxford OX1 3QD, United Kingdom.
Carlos SánchezCenter for Computational Medicine in Cardiology (CCMC), Institute of Computational Science, Università della Svizzera italiana, Lugano, Switzerland.
Xin ZhouDepartment of Computer Science, University of Oxford, Parks Road, Oxford OX1 3QD, United Kingdom.
Annamaria CarusiMedical Humanities, University of Sheffield, United Kingdom.
T Alexander QuinnDepartment of Physiology and Biophysics, Dalhousie University, Halifax, Nova Scotia, Canada.
Kevin BurrageDepartment of Computer Science, University of Oxford, Parks Road, Oxford OX1 3QD, United Kingdom; Mathematical Sciences, Queensland University of Technology, Queensland 4072, Australia; ACEMS, ARC Centre of Excellence for Mathematical and Statistical Frontiers, Queensland University of Technology, Queensland 4072, Australia.
Alfonso Bueno-OrovioDepartment of Computer Science, University of Oxford, Parks Road, Oxford OX1 3QD, United Kingdom.
Blanca RodriguezDepartment of Computer Science, University of Oxford, Parks Road, Oxford OX1 3QD, United Kingdom. Electronic address: blanca.rodriguez@cs.ox.ac.uk.

Funding

British Heart Foundation PG/09/066/27898Wellcome Trust 100246Wellcome Trust 100246/Z/12/Z
6 · The paper itself

Abstract

Physiological variability manifests itself via differences in physiological function between individuals of the same species, and has crucial implications in disease progression and treatment. Despite its importance, physiological variability has traditionally been ignored in experimental and computational investigations due to averaging over samples from multiple individuals. Recently, modelling frameworks have been devised for studying mechanisms underlying physiological variability in cardiac electrophysiology and pro-arrhythmic risk under a variety of conditions and for several animal species as well as human. One such methodology exploits populations of cardiac cell models constrained with experimental data, or experimentally-calibrated populations of models. In this review, we outline the considerations behind constructing an experimentally-calibrated population of models and review the studies that have employed this approach to investigate variability in cardiac electrophysiology in physiological and pathological conditions, as well as under drug action. We also describe the methodology and compare it with alternative approaches for studying variability in cardiac electrophysiology, including cell-specific modelling approaches, sensitivity-analysis based methods, and populations-of-models frameworks that do not consider the experimental calibration step. We conclude with an outlook for the future, predicting the potential of new methodologies for patient-specific modelling extending beyond the single virtual physiological human paradigm.

Indexed as

Electrophysiological PhenomenaModels, CardiovascularCalibrationHeartHumansUser-Computer InterfaceAction potentialArrhythmiasCardiac electrophysiologyIn silico high-throughput screeningPhysiological variabilityPopulations of models

Identifiers

PMID26701222
PMCPMC4821179

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.