Prospective in silico trials identify combined SK and K 2 P channel block as an effective strategy for atrial fibrillation cardioversion
Year: 2024
Type: article
Abstract: Virtual evaluation of medical therapy through human‐based modelling and simulation can accelerate and augment clinical investigations. Treatment of the most common cardiac arrhythmia, atrial fibrillation (AF), requires novel approaches. This study prospectively evaluates and mechanistically explains three novel pharmacological therapies for AF through in silico trials, including single and combined SK and K 2 P channel block. AF and pharmacological action were assessed in a large cohort of 1000 virtual patients, through 2962 multiscale simulations. Extensive calibration and validation with experimental and clinical data support their credibility. Sustained AF was observed in 654 virtual patients. In this cohort, cardioversion efficacy increased to 82% (535 of 654) through combined SK+K 2 P channel block, from 33% (213 of 654) and 43% (278 of 654) for single SK and K 2 P blocks, respectively. Drug‐induced prolongation of tissue refractoriness, dependent on the virtual patient's ionic current profile, explained cardioversion efficacy (atrial refractory period increase: 133.0 ± 48.4 ms for combined vs . 45.2 ± 43.0 and 71.0 ± 55.3 ms for single SK and K 2 P block, respectively). Virtual patients cardioverted by SK channel block presented lower K 2 P densities, while lower SK densities favoured the success of K 2 P channel inhibition. Both ionic currents had a crucial role on atrial repolarization, and thus a synergism resulted from the multichannel block. All three strategies, including the multichannel block, preserved atrial electrophysiological function (i.e. conduction velocity and calcium transient dynamics) and thus its contractile properties (safety). In silico trials identify key factors determining treatment success and the combined SK+K 2 P channel block as a promising strategy for AF management. image Key points This is a large‐scale in silico trial study involving 2962 multiscale simulations. A population of 1000 virtual patients underwent three treatments for atrial fibrillation. Single and combined SK+K 2 P channel block were assessed prospectively. The multi‐ion channel inhibition resulted in 82% cardioversion efficacy. In silico trials have broad implications for precision medicine.
Source: The Journal of Physiology
DOI: 10.1113/jp287124
Institution: University of Oxford
Language: English
Subfield: Cardiology and Cardiovascular Medicine
Field: Medicine
Domain: Health Sciences
Open Access status: hybrid
Estimated APC paid: $5,140
Awards: G1260843, G4230537573, A Centre of Excellence in Computational Biomedicine, A Centre of Excellence in Computational Biomedicine, Human in silico clinical trials in post myocardial infarction: mechanistic investigations into phenotypic electromechanical variability and response to treatment, G5589147751, G7940887209
OpenAlex ID: W4404493434
