Molecular basis of arrhythmias. Review uri icon

Overview

abstract

  • The characterization of single gene disorders has provided important insights into the molecular pathogenesis of cardiac arrhythmias. Primary electrical diseases including long-QT syndrome, short-QT syndrome, Brugada syndrome, and catecholaminergic polymorphic ventricular tachycardia have been associated with mutations in a variety of ion channel subunit genes that promote arrhythmogenesis. Pathological remodeling of ionic currents and network properties of the heart critical for normal electrical propagation plays a critical role in the initiation and maintenance of acquired arrhythmias. This review focuses on the molecular and cellular basis of electrical activity in the heart under normal and pathophysiological conditions to provide insights into the fundamental mechanisms of inherited and acquired cardiac arrhythmias. Improved understanding of the basic biology of cardiac arrhythmias holds the promise of identifying new molecular targets for the treatment of cardiac arrhythmias.

publication date

  • October 18, 2005

Research

keywords

  • Arrhythmias, Cardiac
  • Heart
  • Mutation

Identity

Scopus Document Identifier

  • 27144517158

Digital Object Identifier (DOI)

  • 10.1161/CIRCULATIONAHA.104.494476

PubMed ID

  • 16230503

Additional Document Info

volume

  • 112

issue

  • 16