Clinical, Genetic, and Biophysical Characterization of SCN5A Mutations Associated With Atrioventricular Conduction Block

DW Wang, PC Viswanathan, JR Balser, AL George Jr… - Circulation, 2002 - Am Heart Assoc
DW Wang, PC Viswanathan, JR Balser, AL George Jr, DW Benson
Circulation, 2002Am Heart Assoc
Background—Three distinct cardiac arrhythmia disorders, the long-QT syndrome, Brugada
syndrome, and conduction system disease, have been associated with heterozygous
mutations in the cardiac voltage-gated sodium channel α-subunit gene (SCN5A). We
present clinical, genetic, and biophysical features of 2 new SCN5A mutations that result in
atrioventricular (AV) conduction block. Methods and Results—SCN5A was used as a
candidate gene in 2 children with AV block. Molecular genetic studies revealed G to A …
Background Three distinct cardiac arrhythmia disorders, the long-QT syndrome, Brugada syndrome, and conduction system disease, have been associated with heterozygous mutations in the cardiac voltage-gated sodium channel α-subunit gene (SCN5A). We present clinical, genetic, and biophysical features of 2 new SCN5A mutations that result in atrioventricular (AV) conduction block.
Methods and Results SCN5A was used as a candidate gene in 2 children with AV block. Molecular genetic studies revealed G to A transition mutations that resulted in the substitution of serine for glycine (G298S) in the domain I S5-S6 loop and asparagine for aspartic acid (D1595N) within the S3 segment of domain IV. The functional consequences of G298S and D1595N were assessed by whole-cell patch clamp recording of recombinant mutant channels coexpressed with the β1 subunit in a cultured cell line (tsA201). Both mutations impair fast inactivation but do not exhibit sustained non-inactivating currents. The mutations also reduce sodium current density and enhance slower inactivation components. Action potential simulations predict that this combination of biophysical abnormalities will significantly slow myocardial conduction velocity.
Conclusions A distinct pattern of biophysical abnormalities not previously observed for any other SCN5A mutant have been recognized in association with AV block. These data provide insight into the distinct clinical phenotypes resulting from mutation of a single ion channel.
Am Heart Assoc