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Assessment of atrial conduction time in patients with coronary artery ectasia
Cihan Sengul1, Cihan Cevik, Olcay Ozveren
1Division of Cardiology, Camlica Alman Hospital, Istanbul, Turkey.
Insights
Patients with coronary artery ectasia (CAE) exhibit prolonged P-wave dispersion and interatrial conduction delay. These findings suggest potential atrial conduction abnormalities in individuals with CAE.
Area of Science:
- Cardiology
- Electrophysiology
- Diagnostic Imaging
Background:
- Coronary artery ectasia (CAE) is linked to sympathetic overactivity, inflammation, and oxidative stress.
- These factors are also associated with arrhythmias like atrial fibrillation.
- Atrial conduction abnormalities in CAE patients remain understudied, particularly regarding electromechanical delay.
Purpose of the Study:
- To investigate atrial electromechanical delay in patients with coronary artery ectasia (CAE).
- To compare atrial conduction parameters in CAE patients versus those with nonobstructive coronary artery disease (NO-CAD) and healthy controls.
Main Methods:
- Compared electrocardiographic P-wave measurements and echocardiographic atrial electromechanical coupling (AEC) parameters.
- Assessed interatrial conduction delay in 90 patients: 30 with CAE, 30 with NO-CAD, and 30 controls.
- Utilized tissue Doppler echocardiography to evaluate atrial electromechanical delay.
Main Results:
- Patients with CAE showed significantly increased P-wave dispersion and interatrial conduction delay compared to NO-CAD and control groups.
- Higher mitral, septal, and tricuspid AEC were observed in the CAE group.
- Interatrial conduction delay and P-wave dispersion correlated positively with the number of ectatic segments.
Conclusions:
- P-wave dispersion and interatrial conduction delay are prolonged in patients with CAE.
- These findings highlight potential atrial conduction abnormalities in CAE.
- The number of ectatic segments independently predicts interatrial conduction delay.
Background:
Coronary artery ectasia (CAE) is associated with increased sympathetic activity, plasma levels of inflammatory markers, and oxidative stress. These factors can also cause arrhythmias such as atrial fibrillation. Atrial conduction abnormalities in patients with CAE have not been investigated in terms of atrial electromechanical delay obtained by tissue Doppler echocardiography.
Methods:
Ninety patients with pure CAE (n = 30), nonobstructive coronary artery disease (NO-CAD) (n = 30), and angiographically normal coronary arteries "controls" (n = 30) were compared in terms of electrocardiographic P-wave measurements, echocardiographic atrial electromechanical coupling (AEC) parameters, and interatrial conduction delay.
Results:
The mean left atrium diameter in the CAE group was similar to the NO-CAD group but significantly greater than the control group (3.62 ± 0.28 vs 3.46 ± 0.32 vs 3.41 ± 0.31 cm, P = 0.021). P maximum and P-wave dispersion were significantly increased in the CAE group compared to the NOCAD group and the control group (108.6 ± 6.6 vs 97.9 ± 6.6 vs 93.5 ± 6.2, P = 0.0001; 34.4 ± 7.6 vs 23.2 ± 7.8 vs 19.4 ± 7.7 ms, P < 0.0001). Mitral AEC, septal AEC, and tricuspid AEC were significantly higher in the CAE group than the NO-CAD group and the control group (68 ± 4.5 vs 57 ± 4.5 vs 53 ± 4.6 ms, P < 0.0001; 50.7 ± 7 vs 42.7 ± 7 vs 41.7 ± 7.2 ms, P = 0.0001; 47 ± 6.7 vs 39.1 ± 6.7 vs 38.1 ± 6.6 ms, P < 0.0001). Interatrial conduction delay was significantly increased in the CAE group compared to the NO-CAD group and the control group (21 ± 5.5 vs 17.8 ± 5.6 vs 15 ± 5.6 ms, P < 0.0001).The correlation analysis demonstrated that the interatrial conduction delay and P-wave dispersion (Pd) were positively correlated with number of ectatic segments (ESN) (r = 0.41, P = 0.024 vs r = 0.49, P = 0.006). Stepwise multiple linear regression analysis revealed that the ESN was the only independent determinants of interatrial conduction delay (P = 0.024).
Conclusion:
Pd and interatrial conduction delay are prolonged in patients with CAE compared to NO-CAD patients and the healthy controls.
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