The univariable analysis of MVA events during follow-up in the group of 107 patients with no history of SCA or sVT shows the possible influence of such risk factors such as severely reduced LVEF, dilated left atrium, elevated NT-proBNP, the presence of LBBB, AA or nsVT but no impact of sex, family history of SCD or elevated hs-cTnT (Table 4). This evidence concerns the gene TNNT2 and autosomal dominant cerebellar ataxia.