An East Asian Common Variant Vinculin P.Asp841His Was Associated With Sudden Unexplained Nocturnal Death Syndrome in the Chinese Han Population

Abstract

Background We have identified the cardiomyopathy‐susceptibility gene vinculin ( VCL ) mutation M94I may account for a sudden unexplained nocturnal death syndrome ( SUNDS ) case. We addressed whether VCL common variant D841H is associated with SUNDS . Methods and Results In 8 of 120 SUNDS cases, we detected an East Asian common VCL variant p.Asp841His (D841H). Comparing the H841 allele frequency of the general population in the local database (15 of 1818) with SUNDS victims (10 of 240) gives an odds ratio for SUNDS of 5.226 (95% CI , 2.321, 11.769). The VCL ‐D841H variant was engineered and either coexpressed with cardiac sodium channel ( SCN 5A) in HEK 293 cells or overexpressed in human induced pluripotent stem‐cell–derived cardiomyocytes to examine its effects on sodium channel function using the whole‐cell patch‐clamp method. In HEK 293 cells, under physiological pH conditions ( pH 7.4), D841H caused a 29% decrease in peak I N a amplitude compared to wild type ( WT ), whereas under acidotic conditions ( pH 7.0), D841H decreased further to 43% along with significant negative shift in inactivation compared to WT at pH 7.4. In induced pluripotent stem‐cell‐derived cardiomyocytes, similar effects of D841H on I N a were observed. VCL colocalized with SCN 5A at the intercalated disk in human cardiomyocytes. VCL was also confirmed to directly interact with SCN 5A, and VCL ‐D841H did not disrupt the association of VCL and SCN5A. Conclusions A VCL common variant was genetically and biophysically associated with Chinese SUNDS . The aggravation of loss of function of SCN5A caused by VCL ‐D841H under acidosis supports that nocturnal sleep respiratory disorders with acidosis may play a key role in the pathogenesis of SUNDS .