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Circadian modulation of ventricular tachycardia cycle length variability in ICD patients with dilated cardiomyopathy
A G Manolis1, A Katsivas, E Lazaris
1Hellenic Red Cross Hospital, Athens, Greece.
Insights
Ventricular tachycardia (VT) cycle length variability differs between day and night in dilated cardiomyopathy patients. This study found less VT variability during the day, suggesting circadian rhythm influences arrhythmia characteristics.
Area of Science:
- Cardiology
- Electrophysiology
- Medical Devices
Background:
- Ventricular tachycardia (VT) typically shows stable RR intervals after onset.
- Dilated cardiomyopathy (DCM) is a significant risk factor for VT.
- Third-generation implantable cardioverter-defibrillators (ICDs) are used for VT management.
Purpose of the Study:
- To evaluate ventricular tachycardia cycle length (VTCL) variability in DCM patients.
- To assess circadian modulation of VTCL variability.
- To correlate VTCL variability with time of day (day vs. night).
Main Methods:
- Analysis of 83 VT episodes in 10 DCM patients with implanted ICDs.
- Calculation of VTCL variability using the coefficient of variance of RR intervals (CVRR).
- Comparison of CVRR and mean RR intervals between daytime and nighttime VT episodes.
Main Results:
- No significant difference in mean RR intervals between day (335 +/- 29 ms) and night (350 +/- 22 ms).
- Significantly lower CVRR (VTCL variability) during daytime (2.83 +/- 0.52) compared to nighttime (3.36 +/- 0.48) (P = 0.017).
- 55 VT episodes occurred during the day, 28 during the night.
Conclusions:
- Circadian modulation of VTCL variability is present in DCM patients.
- VTCL variability is reduced during daytime compared to nighttime.
- Sympathovagal balance alterations may explain circadian modulation of VTCL variability in DCM.
Abstract:
VT is usually characterized by stability of the RR intervals after a few cycles from the onset. The aim of this study was to evaluate the VT cycle length (VTCL) variability in patients with dilated cardiomyopathy (DCM), in whom a third-generation ICD was previously implanted. Eighty-three episodes of VT were analyzed in 10 patients (8 male, 2 female, 65 +/- 6 years) with DCM, and NYHA Class II (7 patients) or III (3 patients). As an index of VTCL variability, the coefficient of variance of the last 15 consecutive RR intervals (CVRR) of the detected and stored VT by the device was considered. The mean value of the RR intervals and the mean value of CVRR of the VT episodes recorded during day versus night time were compared. Fifty-five VT episodes were recorded during the day and 28 episodes during the night time. The mean RR intervals of VT episodes during day time was 335 +/- 29 ms and during the night time was 350 +/- 22 ms (P = NS). The mean CVRR of VT episodes during day time and night time were 2.83 +/- 0.52 and 3.36 +/- 0.48, respectively (P = 0.017). In conclusion, a circadian modulation of VTCL variability exists in patients with DCM. The VTCL variability is less during day time compared to night time. A possible explanation is a circadian alteration of sympathovagal balance modifying the electrophysiological properties of the arrhythmogenic substrate.
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