Sudden cardiac death in families with premature cardiovascular disease. Issue 3 (17th August 2019)

• Record Type: Journal Article
• Authors: Bruikman, Caroline; de Ronde, Maurice W J; Amin, Ahmed; Levy, Sonja; Lof, Pien; de Ruijter, Ursula; Hovingh, Kees; Tan, Hanno L; Pinto-Sietsma, Sara-Joan
• Is Part Of: Heart. Volume 106:Issue 3(2020)
• Page Start: 228
• Page End: 232
• Publication Date: 2019-08-17
• Subjects: atherosclerosis -- brugada syndrome -- ajmaline -- death -- sudden -- cardiac; Heart -- Diseases -- Treatment -- Periodicals; Cardiology -- Periodicals; 616.12
• DOI: 10.1136/heartjnl-2019-314861
• Languages: English
• ISSNs: 1355-6037

Abstract

Abstract : Objective: Sudden cardiac death (SCD) in families with premature atherosclerosis (PAS) is generally attributed to lethal arrhythmias during myocardial infarction. Yet, such arrhythmias may also arise from non-ischaemic inherited susceptibility. We aimed to test the hypothesis that Brugada syndrome is prevalent among families with PAS in which SCD occurred. Methods: We investigated all patients who underwent Ajmaline testing to screen them for Brugada syndrome because of unexplained familial SCD in the Amsterdam University Medical Centers between 2004 and 2017. We divided the cohort into two groups based on a positive family history for PAS. All individuals with a positive Ajmaline test were screened for SCN5A-mutation. Results: In families with SCD and PAS, the prevalence of positive Ajmaline test was similar to families with SCD alone (22% vs 19%). The number of SCD cases in families with SCD and PAS was higher (2.34 vs 1.63, p<0.001) and SCD occurred at older age in families with SCD and PAS (42 years vs 36 years, p<0.001), while the prevalence of SCN5A mutations was lower (3% vs 18%, p<0.05). Conclusions: Brugada syndrome has a similar prevalence in families with SCD and PAS as in families with SCD alone, although SCD in families with SCD and PAS occurs in more family members and at older age, while SCN5A mutations in these families are rare. This suggests that the SCD occurring in families with PAS could be related to an underlying genetic predisposition of arrhythmias, with a different genetic origin. It could be considered to screen families with SCD and PAS for Brugada syndrome.