Key result
Women with systemic sclerosis exhibited significantly lower heart rate variability, including reduced 24-hour SDNN (136.1 vs 156.6 ms) compared to healthy controls, indicating autonomic imbalance.
Why the study?
Systemic sclerosis leads to cardiovascular involvement and autonomic disorders with sympathetic predominance that can increase cardiovascular mortality, prompting evaluation of HRT and HRV parameters as predictors of increased cardiovascular risk.
Are heart rate turbulence and heart rate variability parameters altered in patients with systemic sclerosis compared to healthy controls?
Case-Control (n=61)
Are heart rate turbulence and heart rate variability parameters altered in patients with systemic sclerosis compared to healthy controls?
Absolute Event Rate: 136.1% vs 156.6%
p-value: p=0.024
Patients with systemic sclerosis exhibit disturbances in heart rate variability and heart rate turbulence, indicating autonomic imbalance and potentially increased cardiovascular risk.
Introduction: Systemic sclerosis (SSc) is a connective tissue disease manifested by progressive fibrosis of many internal organs including the cardiovascular system and development of autonomic disorders with sympathetic predominance. These abnormalities can increase cardiovascular mortality. Aim: To evaluate heart rate turbulence (HRT) and variability (HRV) parameters (indicator of autonomic imbalance) obtained from 24-hour ECG Holter monitoring, as predictors of the increased cardiovascular risk in patients with scleroderma. Material and methods: Thirty-two scleroderma patients and 30 healthy people were included. After clinical examination, ECG, routine laboratory tests and echocardiography, participants performed 24-hour Holter-ECG at home. For HRT assessment, turbulence onset (To) and turbulence slope (Ts) parameters were used. Both time and frequency domain analysis of HRV was used. The HRV circadian rhythm was also evaluated. Results: Time domain: SDNN, SDNN-ix, SDANN and frequency domain: LF, VLF, ULF, NHF, NLF, parameters were lower, while p50NN was higher in SSc as compared to the control group. There was also a loss of the circadian rhythm for r-MSSD and p50NN present in the control group. Abnormal HRT parameters To and/or Ts occurred in the SSc group only. The median value of To = -1.24% and Ts = 11.13 ms/RR did not differ significantly as compared to the control group. Conclusions: The study confirmed the presence of HRV disturbances, including HRV circadian rhythm, as it may seem at an early stage of SSc. The HRT disorders may be characterized by the increasing changes with advancing disease. This indicates the presence of autonomic imbalance and an increased cardiovascular risk.
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Poliwczak et al. (2019) conducted a case-control in Systemic sclerosis (n=61). Systemic sclerosis vs. Healthy controls was evaluated on 24-hour SDNN (Standard deviation of NN intervals) (p=0.024). Women with systemic sclerosis exhibited significantly lower heart rate variability, including reduced 24-hour SDNN (136.1 vs 156.6 ms) compared to healthy controls, indicating autonomic imbalance.
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