ArticleComputing in cardiology2025
Efficient Generation of Populations of Cardiac Models.
Article in Computing in cardiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
Abstract
To model variability of cardiac action potentials (APs), a population of models (PoM) consisting of different sets of a model's parameter values can be created and calibrated to match observed variability in properties such as AP duration (APD). However, producing appropriate parameter sets for the PoM can be difficult and time-consuming. We adapted a particle swarm optimization (PSO) optimization technique to generate a population of models efficiently. Our population PSO (PPSO) algorithm discourages convergence to a local minimum, and instead guides the search to explore low-error areas of parameter space, yielding many parameter sets that can reproduce the variability of biomarkers seen in real tissue data. Using canine ventricular microelectrode recordings and a synthetic dataset, we extracted sets of APD- and voltage-based biomarkers, allowing ±10% and ±30% variations of the base biomarker values to represent variability. We created 5000- and 2500-member PoMs fitting the parameters of the Fenton-Karma (FK) and ten Tusscher-Noble-Noble-Panfilov (TNNP) models to the biomarker ranges using PPSO. Compared to a random approach, our novel PPSO method produced PoMs matching biomarkers with similar coverage of parameter space for both the FK and TNNP cases, but with greater computational efficiency, accepting up to 10 times more candidate parameter sets.
Identifiers
What OpenQuestion holds
Registered trials
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.