Key result
SCN5A loss-of-function mutations account for up to ~30% of diagnosed Brugada syndrome cases.
Why the study?
Despite significant progress in understanding Brugada syndrome over the last two decades, a number of uncertainties and challenges remain.
This review provides an updated overview of Brugada syndrome, emphasizing that while ICD remains the mainstay of therapy, epicardial ablation and quinidine are emerging as important options for high-risk patients.
Informs genetic evaluation in Brugada syndrome; leaves open whether SCN5A status guides emerging therapies beyond ICD.
In 1992, the Brugada brothers published a patient series of aborted sudden death, who were successfully resuscitated from ventricular fibrillation (VF). These patients had a characteristic coved ST-segment elevation in the right precordial leads on their 12-lead electrocardiogram with no apparent structural heart abnormality. This disease was referred to as "right bundle branch block, persistent ST-segment elevation, and sudden death syndrome." The term Brugada syndrome (BrS) was first coined for this new arrhythmogenic entity in 1996. BrS is more prevalent in Southeast Asian ethnic groups and was considered a familial disease due to the presence of syncope and/or sudden deaths in several members of the same family, however, the genetic alteration was only noted in 1998. The genetic characterization of BrS has proven to be challenging. The most common and well-established BrS genotype involves loss-of-function mutations in the SCN5A gene, but only represents between 15% and 30% of the diagnosed patients. Patients with BrS can present with a range of symptoms which can include syncope, seizures, and nocturnal agonal breathing due to polymorphic ventricular tachycardia or VF. If these arrhythmias are sustained, sudden cardiac death may result. Despite the significant progress on the understanding of BrS over the last two decades, there remain a number of uncertainties and challenges; we present an update review on the subject.
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Hayat et al. (2020) conducted a review in Brugada syndrome. Brugada syndrome is an arrhythmogenic entity characterized by coved ST-segment elevation, with loss-of-function mutations in the SCN5A gene representing 15% to 30% of diagnosed patients.
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