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Published on: December 11, 2017
Atorvastatin therapy increases heart rate variability, decreases QT variability, and shortens QTc interval duration
Bojan Vrtovec1, Renata Okrajsek, Alenka Golicnik
1Division of Cardiology, Ljubljana University Medical Center, Ljubljana, Slovenia.
Insights
Atorvastatin improved heart rate variability (HRV) and QT variability (QTV) in heart failure patients. This statin therapy may reduce arrhythmia risk by decreasing QTc interval.
Area of Science:
- Cardiology
- Pharmacology
- Biomedical Engineering
Background:
- Statins are known to reduce ventricular arrhythmias in atherosclerotic heart disease.
- The antiarrhythmic effects of statins in heart failure patients are not well-defined.
Purpose of the Study:
- To investigate the effects of atorvastatin on heart rate variability (HRV), QT variability (QTV), and QTc interval in patients with advanced heart failure.
- To assess the potential of atorvastatin to mitigate arrhythmia risk in this population.
Main Methods:
- A randomized controlled trial involving 80 heart failure patients.
- 40 patients received atorvastatin; 40 served as controls.
- High-resolution electrocardiogram analysis was used to measure HRV, QTV, and QTc interval at baseline and after 3 months.
Main Results:
- At 3 months, the atorvastatin group showed significantly increased HRV (SDNN and rMSSD) compared to controls.
- The atorvastatin group exhibited significantly decreased QTV (SDNN and rMSSD) and a shorter QTc interval.
- No significant differences in baseline HRV, QTV, or QTc interval were observed between the groups.
Conclusions:
- Atorvastatin administration led to significant improvements in HRV and QTV in heart failure patients.
- The observed decrease in QTc interval suggests a potential reduction in arrhythmia risk.
- Atorvastatin may serve as a therapeutic option to reduce arrhythmia incidence in advanced heart failure.
Background:
Although statins decrease the incidence of ventricular arrhythmias in patients with atherosclerotic heart disease, their potential antiarrhythmic effects in heart failure remain undefined.
Methods And Results:
Of 80 heart failure patients enrolled, 40 were randomized to receive atorvastatin (statin group); the remaining 40 served as controls. At baseline and after 3 months, we measured heart rate variability (HRV), QT variability (QTV), and QTc interval using interactive high-resolution electrocardiogram analysis. The 2 groups did not differ in baseline HRV standard deviation of normal-to-normal intervals (SDNN) (RR): 24.6 +/- 2.8 ms in statin group versus 24.8 +/- 3.1 ms in controls, P = .72; square root of the mean of squared differences between successive intervals (rMSSD) (RR): 21.2 +/- 2.7 ms versus 21.7 +/- 2.9 ms, P = .43), QTV SDNN (QT): 6.4 +/- 1.5 ms versus 6.4+/-1.7, P = .96; rMSSD QT): 9.0 +/- 2.4 ms versus 8.7 +/- 2.9 ms, P = .65, and QTc interval 450 +/- 30 ms versus 446 +/- 27 ms, P = .59. At 3 months, the statin group displayed higher HRV SDNN RR): 27.2 +/- 4.9 ms versus 24.4 +/- 2.8 ms in controls, P = .003; rMSSD RR: 24.7 +/- 4.2 ms versus 21.3 +/- 5.6 ms, P = .004, lower QTV SDNN (QT): 5.1 +/- 1.9 ms versus 6.5 +/- 2.1, P = .004; rMSSD (QT): 6.6 +/- 2.8 ms versus 8.8 +/- 3.1 ms, P = .002, and shorter QTc interval 437 +/- 29 ms versus 450 +/- 25 ms, P = .03 than the control group.
Conclusions:
Atorvastatin increases HRV, decreases QTV, and shortens QTc interval, and may thereby reduce the risk of arrhythmias in patients with advanced heart failure.
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