The autonomic nervous system (ANS) plays a crucial role in cardiovascular regulation by modulating heart rate in response to endogenous and environmental stimuli. Heart rate variability (HRV) analysis has been widely used as a non-invasive tool to assess autonomic function and the balance between sympathetic and parasympathetic activity. Although the physiological interpretation of some HRV parameters remains debated-particularly the low-frequency (LF) spectral component as an index of sympathetic activation-HRV remains an important method for evaluating autonomic cardiovascular control. Reduced HRV has been associated with adverse outcomes in several pathological conditions and physiologically declines with aging, mainly due to progressive neuronal loss at central and spinal levels. Among conditions characterized by autonomic dysfunction, cardiovascular autonomic neuropathy (CAN) represents a common complication of diabetes mellitus (DM) and metabolic syndrome. CAN, defined as impairment of autonomic control of the cardiovascular system, develops early in the disease course and is associated with increased mortality and a higher risk of cardiovascular and renal complications. Sodium-glucose cotransporter 2 inhibitors (SGLT2i), initially developed as glucose-lowering agents, have demonstrated significant cardiovascular and renal protective effects beyond glycemic control. Growing evidence suggests that these drugs exert sympathoinhibitory effects that may be beneficial not only in diabetic patients but also in conditions characterized by sympathetic overactivity. Preclinical and clinical studies have shown that SGLT2i influence autonomic regulation, including sympathetic control of renal function, with reported improvements in 24-hour blood pressure regulation and HRV parameters. Large randomized trials have further confirmed the cardioprotective effects of SGLT2i therapy. Studies such as EMBODY, EMPEROR-Reduced, and EMPEROR-Preserved have demonstrated improvements in HRV indices and significant reductions in cardiovascular death and hospitalization for heart failure, irrespective of diabetic status. Despite these findings, the mechanisms underlying these benefits remain incompletely understood. While reduced sympathetic activity has been proposed as a key mechanism, emerging evidence suggests that SGLT2i may also enhance vagal modulation. Therefore, the present study aims to investigate, in a larger population, the effects of SGLT2i therapy on sympathovagal balance using both spectral HRV parameters and additional indices, including the parasympathetic nervous system index (PNSi), sympathetic nervous system index (SNSi), and the Baevsky Stress Index.
Study Type
OBSERVATIONAL
Enrollment
150
Monitoring of the sympathetic/vagal balance through multiparametric analysis of heart rate variability (HRV) using 24 hours ECG HOLTER
Assessment of the sympathetic/vagal balance at baseline
All outcomes (primary and secondary) will be evaluated at rest, during daily activity and NREM sleep, with short-term (2- and 5-minute) Heart Rate Variability (HRV) analysis from 24-hour Holter recordings, with Kubios Scientific, a gold-standard HRV software tool for research, providing automatic calculation of multiple parameters in the time domain (TD), frequency domain (FD), with non-linear (NL) methods, and automatic time-varying computation of the parasympathetic (PNSi), sympathetic (SNSi), and Baevsky stress (BSTRi) indices, for faster and more comprehensive assessment of cardiac autonomic modulation (the PNS index ranges between -1 and 1 for 68% of the adult population at rest, and similarly scaled SNS index values outside the -1 to 1 range indicate higher or lower than average sympathetic activity) \[1\]. Tables reporting the laboratory's average age-related normal values for all parameters measured in daily activity and NREM sleep are available \[2\]. (Ref. moved to Citations)
Time frame: 24 hours
Changes the sympathetic/vagal balance during pharmacological treatment with SGLT2 inhibitors
Outcome 2 will be assessed with Kubios, measuring the same HRV parameters and indices from the 24-hour follow-up Holter recordings. Changes of the sympathetic/vagal balance will be individually evaluated in each condition (rest, daily activity, and NREM sleep) and compared with the baseline values. No score on a scale will be used.
Time frame: 24 months
Evaluation of diabetic cardiovascular autonomic neuropathy
As for the primary outcome measures, outcome 3 will be assessed with Kubios, measuring the same HRV parameters and indices from the 24-hour baseline and follow-up Holter recordings. The sympathetic/vagal balance will be individually evaluated in each condition (rest, daily activity, and NREM sleep) and compared with the baseline values at each control to identify which HRV parameters/indices can be more sensitive markers for early identification of the onset (or worsening) of diabetic cardiovascular autonomic neuropathy.
Time frame: 24 months
Correlation between improvement of heart failure or cardiorenal disease
Assessment of the possible correlation between improvement of heart failure or cardiorenal disease
Time frame: 24 months
Detection of improvement or normalization of cardiac autonomic balance
Outcome 5 will be assessed with Kubios, measuring the same HRV parameters and indices from the 24-hour baseline and follow-up Holter recordings. The comprehensive assessment of cardiac autonomic modulation will be individually performed in each condition (rest, daily activity, and NREM sleep) by comparing the sensitivity of TD, FD, and NL methods, with that provided by the automatic time-varying computation of the PNSi, SNSi, and BSTRi indices. Any change of the cardiac autonomic modulation toward a prevalence of the parasympathetic tone (either for an increase of vagal modulation, or a decrease of sympathetic modulation, or both), will be considered a positive outcome on cardiac autonomic function \[3-5\].
Time frame: 24 months
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