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Cardiac deceleration capacity and acceleration capacity have diagnostic value in patients with vasovagal syncope
Jijing Wang1, Jinyi Xu1, Yanyan Qiu1
1Department of Cardiopulmonary Function, Zhengzhou University People's Hospital (Henan Provincial People's Hospital), Zhengzhou, Henan, China.
Insights
Deceleration capacity (DC) and acceleration capacity (AC) indicate autonomic regulation. This study found higher DC and lower AC in vasovagal syncope (VVS) patients, suggesting their diagnostic value for VVS.
Area of Science:
- Cardiology
- Autonomic Nervous System Function
Background:
- Deceleration capacity (DC) and acceleration capacity (AC) are key metrics for assessing autonomic regulation.
- Vasovagal syncope (VVS) is a common condition affecting autonomic control.
- Understanding autonomic dysfunction in VVS is crucial for diagnosis and management.
Purpose of the Study:
- To evaluate autonomic nervous system function in patients diagnosed with VVS.
- To determine the diagnostic utility of DC and AC in identifying VVS.
Main Methods:
- Recruited 94 VVS patients and 76 healthy controls.
- Collected 24-hour ECG, echocardiogram, and biochemical data.
- Compared DC, AC, and heart rate variability (HRV) between groups.
Main Results:
- VVS patients showed significantly higher DC (9.3±2.1 ms vs. 7.4±1.4 ms) and lower AC (-9.3±2.1 ms vs. -7.3±1.3 ms) compared to controls.
- Both DC and AC were independently associated with syncope (OR=1.746, P<.001 for DC; OR=0.553, P<.001 for AC).
- ROC analysis indicated AUCs of 0.755 for DC and 0.765 for AC in predicting syncope.
Conclusions:
- Patients with VVS exhibit distinct alterations in autonomic function, characterized by increased DC and decreased AC.
- DC and AC serve as independent predictors of syncope.
- Specific thresholds (DC >9.0 ms, AC < -9.0 ms) may aid in monitoring cardiac autonomic dysfunction in VVS.
Background:
Deceleration capacity (DC) and acceleration capacity (AC) are used to characterize autonomic regulation. The purpose of this study was to evaluate the autonomic nervous function in patients with vasovagal syncope (VVS) and to evaluate the diagnostic value of DC and AC for VVS.
Methods:
A total of 94 consecutive patients with VVS [51.0 (38.0-60.0) years; 48 males] and 76 healthy subjects [53.0 (44.3-62.8) years; 46 males] were recruited as controls. The study compared DC, AC, and heart rate variability (HRV) in 24-h ECG, echocardiogram, and biochemical examinations between the two groups.
Results:
DC was significantly higher (9.3 ± 2.1 vs. 7.4 ± 1.4 ms, p < .001) and AC was lower (-9.3 ± 2.1 vs. -7.3 ± 1.3 ms, p < .001) in the syncope group compared to the control group. HRV indicators were higher in the syncope group. In multivariable analyses, DC [odds ratio = 1.746 (95% CI, 1.389-2.195); p < .001], AC [odds ratio = 0.553 (95% CI, 0.435-0.702); p < .001] were independently associated with syncope. Mean HR was associated with syncope only in patients <60 years of age. Receiver operating characteristics (ROC) curves showed areas under curve (AUC) of DC/AC for predicting syncope are 0.755/0.765 with sensitivity of 56.4%/60.6% and specificity of 93.4%/88.2%.
Conclusion:
Patients with VVS exhibit higher DC and lower AC. Both DC and AC are independently correlated with syncope. A DC value >9.0 ms and an AC value -9.0 ms could potentially be valuable indicators for monitoring cardiac autonomic nervous dysfunction.
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