Auditory stimuli as a trigger for arrhythmic events differentiate HERG- related (LQTS2) patients from KVLQT1-related patients (LQTS1)

AbstractObjectiveThis study was performed to identify a possible relationship between genotype and phenotype in the congenital familial long QT syndrome (cLQTS).BackgroundThe cLQTS, which occurs as an autosomal dominant or recessive trait, is characterized by QT-interval prolongation on the electrocardiogram and torsade de pointes arrhythmias, which may give rise to recurrent syncope or sudden cardiac death. Precipitators for cardiac events are exercise or emotion and occasionally acoustic stimuli.MethodsThe trigger for cardiac events (syncope, documented cardiac arrhythmias, sudden cardiac death) was analyzed in 11 families with a familial LQTS and a determined genotype.ResultsThe families were subdivided in KVLQT1-related families (LQTS1, n = 5) and HERG (human ether-a-gogo-related gene)-related families (LQTS2, n = 6) based on single-strand conformation polymorphism analysis and sequencing. Whereas exercise-related cardiac events dominate the clinical picture of LQTS1patients, auditory stimuli as a trigger for arrhythmic events were only seen in LQTS2patients.ConclusionsArrhythmic events triggered by auditory stimuli may differentiate LQTS2from LQTS1patients