期刊
HEART RHYTHM
卷 13, 期 1, 页码 165-174出版社
ELSEVIER SCIENCE INC
DOI: 10.1016/j.hrthm.2015.07.027
关键词
Carnitine deficiency; Short QT syndrome; Electrophysiological remodeling; Sudden death; Ventricular arrhythmias
资金
- Groupe de Reflexion sur la Recherche Cardiovasculaire (GRRC)
BACKGROUND Short QT syndrome is associated with an increased risk of cardiac arrhythmias and unexpected sudden death. Until now, only mutations in genes encoding the cardiac potassium and calcium channels have been implicated in early T-wave repolarization. OBJECTIVE The purpose of this study was to confirm a relationship between a short QT syndrome and carnitine deficiency. METHODS We report 3 patients affected by primary systemic carnitine deficiency and an associated short QT syndrome. Ventricular fibrillation during early adulthood was the initial symptom in 1 case. To confirm the relationship between carnitine, short QT syndrome, and arrhythmias, we used a mouse model of carnitine deficiency induced by long-term subcutaneous perfusion of MET88. RESULTS MET88-treated mice developed cardiac hypertrophy associated with a remodeling of the mitochondrial network. The continuous monitoring of electrocardiograms confirmed a shortening of the QT interval, which was negatively correlated with the plasma carnitine concentration. As in humans, such alterations coincided with the genesis of ventricular premature beats and ventricular tachycardia and fibrillation. CONCLUSION Altogether, these results suggest that long-chain fatty acid metabolism influence the morphology and the electrical function of the heart.
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