Channelpedia

PubMed 20564468


Referenced in Channelpedia wiki pages of: none

Automatically associated channels: Nav1.5



Title: A homozygous SCN5A mutation in a severe, recessive type of cardiac conduction disease.

Authors: Axel Neu, Michele Eiselt, Matthias Paul, Kathrin Sauter, Birgit Stallmeyer, Dirk Isbrandt, Eric Schulze-Bahr

Journal, date & volume: Hum. Mutat., 2010 Aug , 31, E1609-21

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/20564468


Abstract
Cardiac sodium channels are key players in the generation and propagation of action potentials in the human heart. Heterozygous mutations in the SCN5A gene have been found to be associated with long QT syndrome, Brugada syndrome, and sinus node dysfunction (SND). Recently, overlapping arrhythmia phenotypes have been reported as well. Here we describe a novel recessive SCN5A mutation in a family originating from the German minority in White Russia. Four affected children with a history of early cardiac arrhythmia encompassing SND, conduction disease, and severe ventricular arrhythmias, are homozygous carriers of a novel SCN5A missense mutation (p.I230T) in the channel protein. Interestingly, the heterozygous mutation carriers had neither significant ECG abnormalities nor a history of cardiac events. Heterologous expression of SCN5A(I230T) channels revealed normal protein transport but altered biophysical sodium channel properties. Voltage range of both activation and inactivation were shifted in a way that resulted in decreased sodium current and loss of channel function. In conclusion, we describe a rare clinical condition with a novel SCN5A mutation causing a new type of complex cardiac arrhythmia. Unlike most previously reported sodium channelopathies, this overlap syndrome displays recessive inheritance characteristics and does not seem to follow simple Mendelian rules.