Key result
SNPs known to modulate ECG traits in the general population do not markedly affect ECG traits during acute myocardial infarction nor the risk of ventricular fibrillation.
Why the study?
Do SNPs that modulate ECG traits in the general population affect ECG traits and ventricular fibrillation risk during acute STEMI?
Case-Control (n=969)
Do SNPs that modulate ECG traits in the general population affect ECG traits and ventricular fibrillation risk during acute STEMI?
SNPs that modulate ECG traits in the general population have effects during acute STEMI that are too small to explain ECG differences or determine the risk of ventricular fibrillation.
General-population ECG SNPs lack utility for VF risk assessment in acute STEMI; leaves open discovery of ischemia-specific genetic modifiers.
BACKGROUND: Ventricular fibrillation (VF) in the setting of acute ST elevation myocardial infarction (STEMI) is a leading cause of mortality. Although the risk of VF has a genetic component, the underlying genetic factors are largely unknown. Since heart rate and ECG intervals of conduction and repolarization during acute STEMI differ between patients who do and patients who do not develop VF, we investigated whether SNPs known to modulate these ECG indices in the general population also impact on the respective ECG indices during STEMI and on the risk of VF. METHODS AND RESULTS: The study population consisted of participants of the Arrhythmia Genetics in the NEtherlandS (AGNES) study, which enrols patients with a first STEMI that develop VF (cases) and patients that do not develop VF (controls). SNPs known to impact on RR interval, PR interval, QRS duration or QTc interval in the general population were tested for effects on the respective STEMI ECG indices (stage 1). Only those showing a (suggestive) significant association were tested for association with VF (stage 2). On average, VF cases had a shorter RR and a longer QTc interval compared to non-VF controls. Eight SNPs showed a trend for association with the respective STEMI ECG indices. Of these, three were also suggestively associated with VF. CONCLUSIONS: RR interval and ECG indices of conduction and repolarization during acute STEMI differ between patients who develop VF and patients who do not. Although the effects of the SNPs on ECG indices during an acute STEMI seem to be similar in magnitude and direction as those found in the general population, the effects, at least in isolation, are too small to explain the differences in ECGs between cases and controls and to determine risk of VF.
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Pazoki et al. (2013) conducted a case-control in Acute ST elevation myocardial infarction (STEMI) with or without ventricular fibrillation (n=969). SNPs known to modulate ECG traits (RR, PR, QRS, QTc) vs. Non-carriers or alternative alleles was evaluated on Association of ECG-modulating SNPs with STEMI ECG indices and risk of ventricular fibrillation. SNPs known to modulate ECG traits in the general population do not markedly affect ECG traits during acute myocardial infarction nor the risk of ventricular fibrillation.
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