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Published on: March 3, 2023
Comparison of Heart Rate Variability in People With Diabetes-Related Neuropathic Foot to Their Counterparts Without a
Murong Wu1, Shuang Lin1, Yan Liu2
1Diabetic Foot Care Center, Department of Endocrinology and Metabolism, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Insights
Diabetic foot ulceration (DFU) is linked to worse cardiac autonomic function in Type 2 diabetes mellitus (T2DM) patients. Even without peripheral artery disease, DFU patients show significantly impaired heart rate variability (HRV), indicating higher cardiovascular risk.
Area of Science:
- Cardiology
- Diabetology
- Autonomic Neuroscience
Background:
- Diabetic foot ulceration (DFU) is associated with increased cardiovascular mortality in Type 2 diabetes mellitus (T2DM).
- The underlying mechanisms, particularly concerning cardiac autonomic function, remain unclear.
- This study investigates cardiac autonomic function differences between T2DM patients with and without DFU.
Purpose of the Study:
- To compare cardiac autonomic function between T2DM patients with neuropathic DFU and those without DFU.
- To assess heart rate variability (HRV) indices as indicators of cardiac autonomic modulation.
- To identify associations between DFU and impaired cardiac autonomic function.
Main Methods:
- 362 T2DM participants (181 with DFU, 181 without DFU), matched for propensity scores and free of peripheral artery disease (PAD), were analyzed.
- 24-hour ECG Holter monitoring was performed to collect heart rate variability (HRV) data.
- Key HRV indices including SDNN, rMSSD, SDANN, PNN50, LF, HF, and LF/HF ratio were measured.
Main Results:
- Individuals with DFU exhibited significantly lower levels of all assessed HRV indices (SDNN, rMSSD, SDANN, PNN50, LF, HF, LF/HF ratio) compared to those without DFU (p < 0.05).
- Severe impairment of cardiac autonomic modulation (SDNN < 50 ms) was 2.5 times more prevalent in the DFU group (21.6% vs. 8.8%, p < 0.001).
- DFU was independently and negatively associated with all measured HRV parameters (p < 0.05).
Conclusions:
- Diabetic foot ulceration significantly impairs cardiac autonomic function in T2DM patients, even in the absence of PAD.
- Reduced heart rate variability in DFU patients suggests a heightened cardiovascular risk.
- These findings highlight the importance of assessing cardiac autonomic function in T2DM patients with DFU.
Abstract:
Background: The reasons that individuals with diabetic foot ulceration (DFU) have higher cardiovascular mortality than those with Type 2 diabetes mellitus (T2DM) but without DFU remain controversial. We aimed to compare the differences in cardiac autonomic function between individuals with neuropathic DFU and their counterparts without DFU. Methods: Three hundred and sixty-two participants with T2DM (181 with DFU and 181 without DFU) who were free of peripheral artery disease (PAD) were included in the final analysis after propensity score matching (PSM). All individuals underwent a 24-h ECG Holter and used the following indices of heart rate variability (HRV) to assess cardiac autonomic function: the standard deviation of the normal sinus interval (SDNN), the root mean square of successive RR interval differences (rMSSD), the standard deviation of the 5-min average RR intervals (SDANN), the percentage of normal adjacent RR interval difference > 50 ms (PNN50), the low-frequency power (LF), the high-frequency power (HF), and the LF/HF ratio. Results: Individuals with DFU had lower SDNN, LF/HF, PNN50, rMSSD, HF, SDANN, and LF than their counterparts without DFU (all p < 0.05). Individuals with DFU had a 2.5-fold increase in severe impairment of cardiac autonomic modulation (i.e., SDNN < 50 ms) compared to those without DFU (21.6% vs. 8.8%, p < 0.001). DFU was independently and negatively associated with all the abovementioned HRV measures (all p < 0.05). Conclusion: Among people with neuropathic diabetic foot only, cardiac autonomic function was still more severely impaired in individuals with DFU than in their counterparts without DFU. Trial Registration: CHiCTR2300076628.
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