A Mutation in CALM1 Encoding Calmodulin in Familial Idiopathic Ventricular Fibrillation in Childhood and Adolescence

作者：Marsman Roos F; Barc Julien; Beekman Leander; Alders Marielle; Dooijes Dennis; van den Wijngaard Arthur; Ratbi Ilham; Sefiani Abdelaziz; Bhuiyan Zahurul A; Wilde Arthur A M; Bezzina Connie R^*

来源：Journal of the American College of Cardiology, 2014, 63(3): 259-266.

DOI：10.1016/j.jacc.2013.0.7.091

• calmodulin
• exome sequencing
• genetics
• idiopathic ventricular fibrillation
• ventricular arrhythmia.

Objectives This study aimed to identify the genetic defect in a family with idiopathic ventricular fibrillation (IVF) manifesting in childhood and adolescence.
Background Although sudden cardiac death in the young is rare, it frequently presents as the first clinical manifestation of an underlying inherited arrhythmia syndrome. Gene discovery for IVF is important as it enables the identification of individuals at risk, because except for arrhythmia, IVF does not manifest with identifiable clinical abnormalities.
Methods Exome sequencing was carried out on 2 family members who were both successfully resuscitated from a cardiac arrest. We characterized a family presenting with a history of ventricular fibrillation (VF) and sudden death without electrocardiographic or echocardiographic abnormalities at rest. Two siblings died suddenly at the ages of 9 and 10 years, and another 2 were resuscitated from out-of-hospital cardiac arrest with documented VF at ages 10 and 16 years, respectively. Exome sequencing identified a missense mutation affecting a highly conserved residue (p.F9OL) in the CALM1 gene encoding calmodulin. This mutation was also carried by 1 of the siblings who died suddenly, from whom DNA was available. The mutation was present in the mother and in another sibling, both asymptomatic but displaying a marginally prolonged QT interval during exercise.
Conclusions We identified a mutation in CALM1 underlying IVF manifesting in childhood and adolescence. The causality of the mutation is supported by previous studies demonstrating that F90 mediates the direct interaction of CaM with target peptides. Our approach highlights the utility of exome sequencing in uncovering the genetic defect even in families with a small number of affected individuals.

• 出版日期2014-1-28