Desmin p.R406W mutation is associated with arrhythmias through structural and electrophysiological remodeling

Geryk, M.; Stervinou, T.; Bouaud, M.; Cimarosti, B.; Montnach, J.; Tessier, A.; Jouve, C.; Lindenbaum, P.; Kyndt, F.; Boissard, A.; Henry, C.; Hocini, M.; Batonnet-Pichon, S.; Lauzier, B.; Lamirault, G.; Guillonneau, F.; Hulot, J.-S.; Baro, I.; Gaborit, N.; Le Marec, H.; Haissaguerre, M.; Probst, V.; Schott, J.-J.; Gourraud, J.-B.; Charpentier, F.

doi:10.64898/2026.08.05.742729

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bioRxiv · 10.64898/2026.08.05.742729

Desmin p.R406W mutation is associated with arrhythmias through structural and electrophysiological remodeling

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Abstract

Background and AimsMutations in the desmin (DES) gene cause a variety of cardiomyopathies associated with arrhythmias, yet the electrophysiological consequences of these variants remain largely uncharacterized. The aim of this study was to investigate the pathogenic mechanisms of the de novo DES p.R406W variant, which was identified in a 9-year-old patient who suffered from severe ventricular arrhythmias and sudden cardiac death without overt structural heart disease. MethodsHuman induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) carrying the DES p.R406W variant (including the patients line) were compared to isogenic controls. Action potentials (AP) of hiPSC-CMs were recorded using patch-clamp. Furthermore, 3D engineered heart tissues (EHTs) were generated from hiPSC-CMs and their APs were recorded with sharp microelectrodes. Analytical techniques also included transmission electron microscopy (TEM) and integrated transcriptomic and proteomic profiling. Finally, a heterozygous knock-in (KI) mouse model carrying the Des p.R405W ortholog was evaluated through surface ECG, echocardiography and ex vivo cardiac optical mapping. ResultsThe DES p.R406W mutation prolonged AP duration in IM-R406W hiPSC-CMs and EHTs vs Control ones. Multi-omics analysis of EHTs revealed a dysregulation of genes and proteins involved in contractile function, cell adhesion, and electrical activity. TEM imaging revealed changes in Z-disc architecture in mutant tissues. Twenty-week-old Des p.R405W KI mice exhibited ventricular conduction slowing (prolonged QRS) and a high susceptibility to ventricular tachyarrhythmias, likely due to reentrant mechanisms. Mild hypertrophy was also observed, but only in females. ConclusionThe DES p.R406W variant is highly pathogenic, causing electrical and structural remodeling of the myocardium. This study highlights the effectiveness of hiPSC-CMs and EHTs in recapitulating the clinical phenotype of desminopathy, providing a platform for investigating the mechanisms of early-onset cardiac arrhythmias and SCD.

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Geryk, M., Stervinou, T., Bouaud, M., Cimarosti, B., Montnach, J., Tessier, A., Jouve, C., Lindenbaum, P., Kyndt, F., Boissard, A., Henry, C., Hocini, M., Batonnet-Pichon, S., Lauzier, B., Lamirault, G., Guillonneau, F., Hulot, J.-S., Baro, I., Gaborit, N., Le Marec, H., Haissaguerre, M., Probst, V., Schott, J.-J., Gourraud, J.-B., Charpentier, F.. 2026-08-11. Desmin p.R406W mutation is associated with arrhythmias through structural and electrophysiological remodeling. https://doi.org/10.64898/2026.08.05.742729

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