ArticleEuropace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology2026
Sex-specific virtual population for the prediction and assessment of arrhythmia risk.
Article in Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology, 2026. 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
7 authors.
Funding
Abstract
aimsWomen are at higher risk of serious ventricular arrhythmias, including torsades de pointes, when repolarization reserve is reduced, but sex-stratified mechanisms and quantitative risk assessment remain challenging. We aimed to develop scalable, tissue-scale, sex-aware ventricular virtual populations to quantify and explain sex differences in inherited and acquired proarrhythmic susceptibility. METHODS AND
resultsWe constructed male and female virtual cohorts using a one-dimensional ventricular cable model with pseudo-electrocardiogram (pseudo-ECG), integrating sex-specific ionic conductance backgrounds and acute sex-hormone modulation. Virtual populations were filtered under multi-condition stress tests and calibrated to clinical corrected QT interval (QTc) distributions. We generated long QT syndrome types 1-3 (LQT1-3) cohorts, simulated sympathetic stress, and performed virtual drug trials for 109 compounds using multichannel block profiles at 1× effective free therapeutic plasma concentration. Proarrhythmic risk was defined by tissue-scale instability events (premature ventricular complexes, T-wave alternans, or repolarization failure). Drivers were analysed using regression and channel-sensitivity analysis, and clinical 24 h concentration-ECG data after dosing were used for external validation. The female cohorts exhibited higher simulated event risk across long QT syndrome subtypes and across multichannel drug block profiles, including drugs with <10 ms mean QTc prolongation. Female-to-male risk ratios tracked clinical risk categories. Simulated QTc time-courses and concentration-QTc trends agreed with 24 h clinical ECG data for key reference drugs.
conclusionSex-aware tissue-scale virtual populations enable in silico trials that quantify proarrhythmic risk beyond mean ΔQTc, provide mechanistic drivers, and support sex-informed cardiac safety evaluation and monitoring strategies.
Indexed as
Identifiers
What Socratic 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 Socratic graph.