Prospective in silico trials identify combined SK and K2P channel block as an effective strategy for atrial fibrillation cardioversion

Journal article

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 K₂P 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+K₂P channel block, from 33% (213 of 654) and 43% (278 of 654) for single SK and K2P 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 K₂P block, respectively). Virtual patients cardioverted by SK channel block presented lower K₂P densities, while lower SK densities favoured the success of K₂P 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+K₂P channel block as a promising strategy for AF management.

Authors: Dasí, A; Arantes Berg, L; Martinez-Navarro, H; Bueno Orovio, A; Rodriguez, B

• Publication status: Published
• Peer review status: Peer reviewed
• Publisher: Wiley
• Journal: The Journal of Physiology
• Place of publication: England
• Publication date: 2024-11-18
• Acceptance date: 2024-10-23
• DOI: 10.1113/jp287124
• EISSN: 1469-7793
• ISSN: 0022-3751
• Pmid: 39557619
• Language: English
• Keywords: K2P channels; virtual patients; in silico trials; pharmacological therapy; atrial fibrillation; SK channels