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Measuring Cardiac Autonomic Nervous System (ANS) Activity in Children
Published on: April 29, 2013
Evaluation of cardiac autonomic functions in patients with systemic lupus erythematosus
H Yorgun1, U Canpolat, K Aytemir
1Polatlı Duatepe State Hospital, Ankara, Turkey.
Insights
Systemic lupus erythematosus (SLE) patients show impaired cardiac autonomic functions, including heart rate recovery and heart rate variability, even without overt symptoms. These findings highlight potential risks and the need for further investigation into autonomic dysfunction in SLE.
Area of Science:
- Cardiology
- Rheumatology
- Autonomic Nervous System Research
Background:
- Cardiovascular disease is a leading cause of mortality in Systemic Lupus Erythematosus (SLE).
- Cardiac autonomic dysfunction may precede or accompany overt cardiac involvement in SLE patients.
Purpose of the Study:
- To investigate cardiac autonomic functions in patients with SLE.
- To assess heart rate recovery (HRR), heart rate variability (HRV), heart rate turbulence (HRT), and QT dispersion in SLE patients compared to healthy controls.
Main Methods:
- Enrolled 36 SLE patients and 32 healthy controls for 24-h Holter monitoring.
- Calculated HRR indices, analyzed HRV (including SDNN, SDANN, RMSSD, PNN50, LF, HF), HRT, and QT dispersion.
- Compared autonomic function parameters between SLE patients and the control group.
Main Results:
- SLE patients exhibited significantly impaired HRR, reduced HRV (lower SDNN, SDANN, RMSSD, PNN50, HF; higher LF/HF ratio), and altered HRT.
- Increased QT dispersion was observed in SLE patients compared to controls.
- These autonomic function abnormalities were present despite the absence of overt cardiac symptoms in SLE patients.
Conclusions:
- Cardiac autonomic functions are significantly impaired in SLE patients, irrespective of clinical cardiac involvement.
- Impaired autonomic function may represent an early marker of cardiovascular risk in SLE.
- Further research is warranted to understand the prognostic significance and clinical implications of these findings in SLE management.
Background:
Cardiovascular involvement is one of the leading causes of death among patients with systemic lupus erythematosus (SLE). In this study, we aimed to investigate cardiac autonomic functions in SLE patients.
Methods:
We enrolled 36 patients (25 female; mean age 34.2 ± 10.2 years) with SLE and 32 healthy subjects (23 female; mean age 35.0 ± 10.3 years). All participants underwent 24-h Holter recording. Heart rate recovery (HRR) indices were calculated by subtracting first, second, and third-minute heart rates from maximal heart rate. All patients underwent heart rate variability (HRV), heart rate turbulence (HRT) and QT dispersion analysis. The mean SLE duration was 8.4 ± 4.0 years.
Results:
According to the baseline demographic characteristics, both groups were similar with regard to age, gender, body mass index and left ventricular ejection fraction. Mean HRR1 (32.6 ± 10.9 vs. 42.5 ± 6.5, p = 0.038), HRR2 (51.0 ± 16.9 vs. 61.0 ± 10.8, p = 0.01) and HRR3 (52.8 ± 17.5 vs. 65.8 ± 9.8, p < 0.001) values were significantly higher in control group. When HRV was considered, SDNN, SDANN, RMSSD, PNN50 and high frequency (HF) component were significantly decreased in patients with SLE compared with healthy controls, but low frequency (LF) component and LF/HF were significantly higher in SLE patients. In addition, HRT onset and HRT slope values were significantly less negative in SLE patients. QT dispersion was significantly greater in SLE patients than healthy subjects (81.3 ± 15.8 vs. 53.2 ± 13.1, p < 0.001).
Conclusion:
Our study results suggest that cardiac autonomic functions are impaired in SLE patients despite the absence of overt cardiac involvement and symptoms. Further studies are needed to elucidate the prognostic significance and clinical implications of impaired autonomic functions in patients with SLE.
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