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Heart rate variability in patients with stable coronary artery disease and aspirin resistance
Tahir Durmaz1, Telat Keles, Ozcan Ozdemir
1Ataturk Education and Research Hospital, Ankara, Turkey.
Insights
Aspirin resistance in stable coronary artery disease patients is linked to reduced heart rate variability (HRV) and increased sympathetic activity. This association may elevate the risk of recurrent myocardial ischemia and cardiovascular death.
Area of Science:
- Cardiology
- Clinical Medicine
- Physiology
Background:
- Aspirin resistance, defined by impaired thromboxane synthesis inhibition, is a known risk factor for adverse cardiovascular events.
- Heart rate variability (HRV) analysis is a valuable tool for risk stratification in patients with cardiac conditions.
- The relationship between aspirin resistance and HRV in stable coronary artery disease (CAD) requires further elucidation.
Purpose of the Study:
- To investigate the association between heart rate variability (HRV) parameters and aspirin resistance in patients with stable coronary artery disease (CAD).
Main Methods:
- Sixty-nine patients with stable CAD were assessed for aspirin response.
- Heart rate variability (HRV) was analyzed using various time-domain and frequency-domain parameters.
- Platelet aggregation and clinical parameters were also evaluated.
Main Results:
- Aspirin resistance was identified in 26% of patients.
- Aspirin non-responders exhibited significantly lower HRV (e.g., HF, SDNN) and higher sympathetic activity (e.g., LF/HF ratio) compared to responders.
- Left ventricular ejection fraction and aspirin resistance were identified as key predictors of reduced SDNN and elevated LF/HF ratio.
Conclusions:
- Aspirin resistance in stable CAD patients is associated with diminished heart rate variability and heightened sympathetic nervous system activity.
- These HRV alterations in aspirin-resistant patients may contribute to an increased risk of myocardial ischemia and cardiovascular mortality.
Abstract:
Aspirin resistance as defined by failure to effectively inhibit thromboxane synthesis is associated with a higher risk of recurrent myocardial ischemia and cardiovascular death. Heart rate variability (HRV) analysis has been extensively used to identify patients at risk for increased cardiac mortality. The aim of this study was to evaluate the association between HRV and aspirin resistance in patients with stable coronary artery disease (CAD). Sixty-nine (69) consecutive patients with stable CAD were included in this study. Of the 69 patients, 18 (26%) were aspirin nonresponders. When the aspirin responders were compared with the nonresponders, there was no significant difference between the groups with respect to most clinical parameters, major cardiovascular risk factors, medical treatments, and aspirin dosages. However, the patients with aspirin resistance had a higher previous myocardial infarction history and lower left ventricular ejection fraction. Moreover, mean platelet volume, CT/EPI, CT/ADP values, LF and LF/HF ratio were higher while HF, SDNN, SDANN, and RMSSD were lower in the nonresponder group than the responders. Regarding HRV parameters, CT/ADP time was negatively correlated with SDNN (r = -0.5, P = 0.02) and HF (r = -0.4, P = 0.03), and positively correlated with LF (r = 0.6, P = 0.01) and LF/HF (r = 0.7, P = 0.001). Similarly, CT/EPI time was negatively correlated with SDNN (r = -0.4, P = 0.03), and positively correlated with LF (r = 0.5, P = 0.02) and the LF/HF ratio (r = 0.5, P = 0.02). Regression analysis revealed that the only parameters affecting SDNN and LF/HF ratio were left ventricle ejection fraction and aspirin resistance. The heart rate variability decreased and sympathetic activity increased in the patients with aspirin resistance and stable CAD. This may contribute to a higher risk of recurrent myocardial ischemia and cardiovascular death in patients with aspirin resistance.
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