The Elusive Link Between LQT3 and Brugada Syndrome
Author(s) -
Silvia G. Priori,
Carlo Napolitano,
Peter J. Schwartz,
Raffaella Bloise,
Lia Crotti,
E Ronchetti
Publication year - 2000
Publication title -
circulation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.795
H-Index - 607
eISSN - 1524-4539
pISSN - 0009-7322
DOI - 10.1161/01.cir.102.9.945
Subject(s) - flecainide , medicine , brugada syndrome , qt interval , long qt syndrome , cardiology , atrial fibrillation
Defects of the SCN5A gene encoding the cardiac sodium channel are associated with both the LQT3 subtype of long-QT syndrome and Brugada syndrome (BS). The typical manifestations of long-QT syndrome (QT interval prolongation) and BS (ST segment elevation in leads V1 through V3) may coexist in the same patients, which raises questions about the actual differences between LQT3 and BS. Intravenous flecainide is the standard provocative test used to unmask BS in individuals with concealed forms of the disease, and oral flecainide has been proposed as a treatment option for LQT3 patients because it may shorten their QT interval.
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