Summary
March 2008, Vol. 9, No. 4, Pages 537-549 , DOI 10.1517/14656566.9.4.537

Cardiac sodium channels and inherited electrophysiologic disorders: a pharmacogenetic overview

Jeroen PP Smits1 MD PhD, Marieke T Blom2 MA, Arthur AM Wilde1 MD PhD & Hanno L Tan1,2 MD PhD
1University of Amsterdam, Academic Medical Center, Department of Cardiology, Meibergdreef 9, 1105 AZ Amsterdam, The Netherlands
2University of Amsterdam, Academic Medical Center, Heart Failure Research Center, Meibergdreef 9, 1105 AZ Amsterdam, The Netherlands +31 20 5663264; +31 20 6975458;
Author for correspondence



Sodium (Na) channels are essential for cardiac electrical activity. Cardiac Na channel dysfunction, inherited or acquired, can induce life-threatening conduction and arrhythmia disorders. Inherited Na channel dysfunction may put affected patients at a greater risk for these complications when channel-modifying drugs are prescribed. This study addressed pharmacogenetic effects in three well-described Na channel-related diseases: long QT syndrome type 3, Brugada syndrome and inherited cardiac conduction disease. A review of the currently available literature on cardiac Na channel-modulating drugs was undertaken. An overview is given of the known risks of development of the previously mentioned complications of commonly prescribed drugs in patients affected with Na channel-related diseases and the underlying mechanisms.

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Authors:
Jeroen PP Smits
Marieke T Blom
Arthur AM Wilde
Hanno L Tan
Keywords:
Brugada syndrome
cardiac arrhythmia syndromes
conduction disease
inherited
long QT syndrome type 3
pharmacogenomics
sodium channel