The Brugada syndrome (BrS) is characterized by coved-type ST-segment elevation in the right precordial leads on the electrocardiogram (ECG) and increased risk of sudden cardiac death (SCD). While it is an inheritable disease, determining the true prevalence is a challenge, since patients may report no known family history of the syndrome, present with a normal spontaneous ECG pattern at the time of examination, and test negative for all known BrS-causative genes. In fact, SCD is often the first indication that a person is affected by the syndrome. Men are more likely to be symptomatic than women. Abnormal, low-voltage, fractionated electrograms have been found in the epicardium of the right ventricular outflow tract (RVOT). Ablation of this area abolishes the abnormal electrograms and helps to prevent arrhythmic recurrences. BrS patients are more likely to experience ventricular tachycardia/fibrillation (VT/VF) during fever or during an increase in vagal tone. Isoproterenol helps to reverse the ECG BrS phenotype. In this review, we discuss roles of calcium in various conditions that are relevant to BrS, such as changes in temperature, heart rate, and vagal tone, and the effects of gender and isoproterenol on calcium handling. Studies are warranted to further investigate these mechanisms in models of BrS.
Calcium in Brugada syndrome: Questions for future research / M.M. Monasky, C. Pappone, M. Piccoli, A. Ghiroldi, E. Micaglio, L. Anastasia. - In: FRONTIERS IN PHYSIOLOGY. - ISSN 1664-042X. - 9:AUG(2018), pp. 1088.1-1088.14.
|Titolo:||Calcium in Brugada syndrome: Questions for future research|
|Parole Chiave:||Brugada syndrome; sudden cardiac death; channelopathies; ion channel; fever; genetic testing|
|Settore Scientifico Disciplinare:||Settore BIO/10 - Biochimica|
|Data di pubblicazione:||2018|
|Digital Object Identifier (DOI):||http://dx.doi.org/10.3389/fphys.2018.01088|
|Appare nelle tipologie:||01 - Articolo su periodico|