AUTHOR=Chen Xiu , Barajas-Martínez Hector , Xia Hao , Zhang Zhonghe , Chen Ganxiao , Yang Bo , Jiang Hong , Antzelevitch Charles , Hu Dan 

TITLE=Clinical and Functional Genetic Characterization of the Role of Cardiac Calcium Channel Variants in the Early Repolarization Syndrome

JOURNAL=Frontiers in Cardiovascular Medicine

VOLUME=8

YEAR=2021

URL=https://www.frontiersin.org/journals/cardiovascular-medicine/articles/10.3389/fcvm.2021.680819

DOI=10.3389/fcvm.2021.680819

ISSN=2297-055X

ABSTRACT=<p><bold>Background:</bold> Early repolarization syndrome (ERS) is an inherited sudden cardiac death (SCD) syndrome. The present study investigates the role of genetic variants in cardiac calcium-channel genes in the pathogenesis of ERS and probes the underlying mechanisms.</p><p><bold>Methods:</bold> Polymerase chain reaction–based next-generation sequencing was carried out using a targeted gene approach. Unrelated ERS probands carrying calcium-channel variants were evaluated clinically and compared with matched healthy controls. Wild-type (WT) and mutant <italic>CACNA1C</italic> genes were coexpressed with <italic>CACNB2b</italic> and <italic>CACNA2D1</italic> in HEK293 cells and studied using whole-cell patch-clamp techniques and confocal fluorescence microscope.</p><p><bold>Results:</bold> Among 104 ERS probands, 16 carried pathogenic variants in calcium-channel genes (32.2 ± 14.6 years old, 87.5% male). The symptoms at diagnosis included syncope (56.3%), ventricular tachycardia/fibrillation (62.5%), and SCD (56.3%). Three cases (18.8%) had a family history of SCD or syncope. Eight patients (50.0%) had a single calcium gene rare variant. The other half carried rare variants in other ERS-susceptible genes. Compared with controls, the heart rate was slower (72.7 ± 8.9 vs. 65.6 ± 16.1 beats/min, <sup>*</sup><italic>p</italic> &lt; 0.05), QTc interval was shorter (408.2 ± 21.4 vs. 386.8 ± 16.9 ms, <sup>**</sup><italic>p</italic> &lt; 0.01), and Tp-e/QT was longer (0.22 ± 0.05 vs. 0.28 ± 0.04, <sup>***</sup><italic>p</italic> &lt; 0.001) in single calcium mutation carriers. Electrophysiological analysis of one mutation, <italic>CACNA1C</italic>-P817S (c.2449C&gt;T), revealed that the density of whole-cell calcium current (<italic>I</italic><sub>Ca</sub>) was reduced by ~84.61% compared to WT (−3.17 ± 2.53 vs. −20.59 ± 3.60 pA/pF, <italic>n</italic> = 11 and 15, respectively, <sup>**</sup><italic>p</italic> &lt; 0.01). Heterozygous expression of mutant channels was associated with a 51.35% reduction of <italic>I</italic><sub>Ca</sub>. Steady-state inactivation was shifted to more negative potentials and significantly accelerated as well. Confocal microscopy revealed trafficking impairment of <italic>CACNA1C</italic>-P817S (peripheral/central intensity: 0.94 ± 0.10 in WT vs. 0.33 ± 0.12 in P817S, <italic>n</italic> = 10 and 9, respectively, <sup>**</sup><italic>p</italic> &lt; 0.01).</p><p><bold>Conclusions:</bold> ERS associated with loss-of-function (LOF) genetic defects in genes encoding the cardiac calcium channel represents a unique clinical entity characterized by decreased heart rate and QTc, as well as increased transmural dispersion of repolarization. In the case of <italic>CACNA1C</italic>-P817S, impaired trafficking of the channel to the membrane contributes to the LOF.</p>