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Published on: June 5, 2019
Clinical Evidence of Wearable-Derived Heart Rate Variability for Detecting Systemic Inflammation: A Systematic Review
Rukmono Siswishanto1, Detty Siti Nurdiati1, Irwan Endrayanto Aluicius2
1Department of Obstetrics and Gynecology, Faculty of Medicine, Public Health and Nursing, Universitas Gadjah Mada, Yogyakarta 55281, Indonesia.
Wearable heart rate variability (HRV) shows a consistent inverse link with C-reactive protein (CRP), suggesting it can non-invasively reflect systemic inflammation. However, more research is needed to confirm its clinical usefulness as a biomarker.
Area of Science:
- Biomedical Engineering
- Physiological Monitoring
- Digital Health
Background:
- Wearable devices offer continuous autonomic nervous system (ANS) assessment via heart rate variability (HRV).
- Systemic inflammation impacts ANS balance, making HRV a potential non-invasive biomarker.
- The accuracy of wearable HRV for detecting inflammation needs clarification.
Purpose of the Study:
- To systematically review the clinical relevance of wearable-derived HRV indices against established inflammatory biomarkers.
- To assess the consistency and accuracy of wearable HRV in reflecting inflammatory states.
Main Methods:
- Systematic literature search across major databases (PubMed, Scopus, Web of Science, Cochrane Library) up to April 2025.
- Synthesis Without Meta-analysis (SWiM) framework employed due to methodological heterogeneity.
- Vote counting, effect-direction plots, and sign tests used for data synthesis.
Main Results:
- Eleven studies (2419 participants) were included.
- SDNN (standard deviation of NN intervals) showed a significant inverse association with CRP (p=0.031).
- ECG-based wearables demonstrated more consistent HRV-inflammation associations than photoplethysmography (PPG) devices.
Conclusions:
- Wearable-derived HRV, especially SDNN from ECG devices, correlates inversely with CRP, indicating potential as a systemic inflammation biomarker.
- Heterogeneity and lack of diagnostic accuracy data limit current clinical utility.
- Further validation in standardized studies is required for clinical application.
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