Key result
Novel heterozygous PRKAG2 mutation is linked to familial hypertrophic left ventricular non-compaction cardiomyopathy.
Why the study?
Isolated ventricular noncompaction is a serious cardiomyopathy associated with ventricular dysfunction, thromboembolic events, and rhythm problems, but rhythm abnormalities in children with IVNC are not well characterized.
Observational (n=15)
No
Supports PRKAG2 testing in select hypertrophic LVNC families; leaves open validation in larger, diverse cohorts.
BACKGROUND: Isolated ventricular noncompaction (IVNC) is a serious cardiomyopathy with a generally poor prognosis. It is characterized by the presence of prominent ventricular myocardial trabeculations and deep intertrabecular recesses, in the absence of other structural heart defects. This cardiomyopathy is usually associated with ventricular dysfunction, thromboembolic events, and rhythm problems. METHODS AND RESULTS: This article describes 11 children who have rhythm abnormalities associated with IVNC. On admission, eight children had complaints including palpitation, syncope, heart failure, and bradycardia. Ventricular arrhythmias were diagnosed in four children, sinus node and atrioventricular conductance disturbances in six children, and Wolff-Parkinson-White syndrome and associated tachycardia in one child. Three children with ventricular arrhythmias received an automatic implantable cardioverter defibrillator (ICD). Three patients died of cardiac problems during the follow-up period. CONCLUSION: Since many of rhythm abnormalities, including life-threatening ventricular arrhythmias, may be seen in patients with IVNC, children with IVNC should be screened for arrhythmias. An ICD may be the best treatment for some of these patients.
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Çeliker et al. (2005) conducted an observational in Left ventricular non-compaction cardiomyopathy (LVNC) (n=15). PRKAG2 mutation c.905G>A (p.R302Q) vs. Family members without the mutation was evaluated on Association of PRKAG2 mutation with LVNC phenotype. A missense heterozygous mutation of PRKAG2 [c.905G>A (p.R302Q)] was identified as the potentially pathogenic cause of hypertrophic left ventricular non-compaction cardiomyopathy in a Chinese family.
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