Evidence map›Paper›PMID 31570308›Full record

ArticleMorphologie : bulletin de l'Association des anatomistes2019

Improving the clinical understanding of hypertrophic cardiomyopathy by combining patient data, machine learning and computer simulations: A case study.

A Lyon, A Mincholé, A Bueno-Orovio, B Rodriguez

Abstract read
In one paragraph

Article in Morphologie : bulletin de l'Association des anatomistes, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Review
  2. Computational modelling of biological systems now and then: revisiting tools and visions from the beginning of the century.Philosophical transactions. Series A, Mathematical, physical, and engineering sciences · 2025
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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

4 authors.

A LyonDepartment of Computer Science, University of Oxford, Oxford, United Kingdom; Cardiovascular Research Institute Maastricht (CARIM), Maastricht University, Maastricht, Netherlands.
A MincholéDepartment of Computer Science, University of Oxford, Oxford, United Kingdom.
A Bueno-OrovioDepartment of Computer Science, University of Oxford, Oxford, United Kingdom.
B RodriguezDepartment of Computer Science, University of Oxford, Oxford, United Kingdom. Electronic address: blanca.rodriguez@cs.ox.ac.uk.

Funding

British Heart Foundation FS/17/22/32644National Centre for the Replacement, Refinement and Reduction of Animals in Research NC/P001076/1Wellcome Trust
6 · The paper itself

Abstract

Most patients with hypertrophic cardiomyopathy (HCM), the most common genetic cardiac disease, remain asymptomatic, but others may suffer from sudden cardiac death. A better identification of those patients at risk, together with a better understanding of the mechanisms leading to arrhythmia, are crucial to target high-risk patients and provide them with appropriate treatment. However, this currently remains a challenge. In this paper, we present a successful example of implementing computational techniques for clinically-relevant applications. By combining electrocardiogram and imaging data, machine learning and high performance computing simulations, we identified four phenotypes in HCM, with differences in arrhythmic risk, and provided two distinct possible mechanisms that may explain the heterogeneity of HCM manifestation. This led to a better HCM patient stratification and understanding of the underlying disease mechanisms, providing a step further towards tailored HCM patient management and treatment.

Indexed as

Machine LearningModels, CardiovascularAsymptomatic DiseasesCardiomyopathy, HypertrophicClinical Decision-MakingComputer SimulationDeath, Sudden, CardiacElectrocardiographyHeart VentriclesHumansMagnetic Resonance ImagingPatient SelectionRisk AssessmentRisk FactorsCardiac magnetic resonance imagingComputational clusteringComputer modelinge-cardiologyElectrocardiographyHypertrophic cardiomyopathyPersonalized simulationsPhenotypingVPH

Identifiers

PMID31570308
PMCPMC6913520

What OpenQuestion holds

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Registered trials

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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.