SciELO - Scientific Electronic Library Online

vol.59 número1Acciones de endotelina 1 y angiotensina II en embarazos complicados con preeclampsiaCompuestos disruptores endocrinos y su participación en la programación del eje reproductivo índice de autoresíndice de materiabúsqueda de artículos
Home Pagelista alfabética de revistas  

Revista de investigación clínica

versión impresa ISSN 0034-8376


MEDEIROS-DOMINGO, Argelia et al. New perspectives in long QT syndrome. Rev. invest. clín. [online]. 2007, vol.59, n.1, pp.57-72. ISSN 0034-8376.

Long QT Syndrome (LQTS) is a cardiac channelopathy characterized by prolonged ventricular repolarization and increased risk to sudden death secondary to ventricular dysrrhythmias. Was the first cardiac channelopathy described and is probably the best understood. After a decade of the sentinel identification of ion channel mutation in LQTS, genotype-phenotype correlations have been developed along with important improvement in risk stratification and genetic guided-treatment. Genetic screening has shown that LQTS is more frequent than expected and interestingly, ethnic specific polymorphism conferring increased susceptibility to drug induced QT prolongation and torsades de pointes have been identified. A better understanding of ventricular arrhythmias as an adverse effect of ion channel binding drugs, allow the development of more safety formulas and better control of this public health problem. Progress in understanding the molecular basis of LQTS has been remarkable; eight different genes have been identified, however still 25% of patients remain genotype-negative. This article is an overview of the main LQTS knowledge developed during the last years.

Palabras llave : Sudden death; Long QT Syndrome; Cardiac channelopathies; Arrhythmias.

        · resumen en Español     · texto en Español     · Español ( pdf )


Creative Commons License Todo el contenido de esta revista, excepto dónde está identificado, está bajo una Licencia Creative Commons