Why the study?
Cardiovascular diseases remain the leading cause of mortality worldwide, requiring integrative approaches linking fundamental ion channel and Ca2+ biology to translational therapeutic applications.
Design
White paper and symposium consensus synthesis
Informs clinical arrhythmia management; extends research by integrating ion channel and Ca2+ signaling mechanisms across scales.
Cardiovascular diseases remain the leading cause of mortality worldwide, driven by complex, multiscale mechanisms that span molecular, cellular and organ-level dysfunction. Effective therapeutic strategies therefore require integrative approaches that link fundamental biology to translational applications. The 8th UC Davis CardioVascular Symposium gathered experts in ion channel biophysics, Ca²⁺ signalling, arrhythmia mechanisms and cardiovascular physiology to discuss recent advances and define emerging priorities. This white paper synthesizes the key themes and consensus points that emerged, highlighting progress in two core domains: (1) advances in cardiovascular electrophysiology and arrhythmia mechanisms, and (2) spatiotemporal dynamics of Ca²⁺ signalling in cardiac and vascular function and remodelling. We also identify conceptual and technical challenges that must be addressed to accelerate therapeutic discovery and emphasize cross-cutting opportunities where experimental and computational approaches can converge. By integrating ion channel biology and Ca²⁺ signalling mechanisms across scales, this work outlines new directions for advancing cardiovascular research and treatment.
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Marchianò et al. (2026) studied this question.
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