Frontiers in physiology · 2025
A novel kinetic model estimating the urea concentration in plasma during non-invasive sweat-based monitoring in hemodialysis.
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Yin Xiaoyu, Adelaars Sophie, Peri Elisabetta, Pelssers Eduard, Den Toonder Jaap, Bouwman Arthur, Van de Kerkhof Daan, Mischi Massimo
Аннотация
INTRODUCTION: The adequacy of hemodialysis (HD) in patients with end-stage renal disease is evaluated frequently by monitoring changes in blood urea concentrations multiple times between treatments. As monitoring of urea concentrations typically requires blood sampling, the development of sweat-sensing technology offers a possible less-invasive alternative to repeated venipuncture. Moreover, this innovative technology could enable personalized treatment in a home-based setting. However, the clinical interpretation of sweat monitoring is hampered by the limited literature on the correlation between urea concentrations in sweat and blood. This study introduces a pioneering approach to estimate blood urea concentrations using sweat urea concentration values as input.
METHODS: To simulate the complex transport mechanisms of urea from blood to sweat, a novel pharmacokinetic transport model is proposed. Such a transport model, together with a double-loop optimization strategy from our previous work, was employed for patient-specific estimation of blood urea concentration. 32 patient samples of paired sweat and blood urea concentrations, collected both before and after HD, were used to validate the model.
RESULTS: This resulted in an excellent Pearson correlation coefficient (0.98, 95%CI: 0.95-0.99) and a clinically irrelevant bias (-0.181 mmol/L before and -0.005 mmol/L after HD).
DISCUSSION: This model enabled the accurate estimation of blood urea concentrations from sweat measurements. By accurately estimating blood urea concentrations from sweat measurements, our model enables non-invasive and more frequent assessments of dialysis adequacy in ESRD patients. This approach could facilitate home-based and patient-friendly dialysis management, enhancing patient comfort while enabling more personalized treatment across diverse clinical settings.
METHODS: To simulate the complex transport mechanisms of urea from blood to sweat, a novel pharmacokinetic transport model is proposed. Such a transport model, together with a double-loop optimization strategy from our previous work, was employed for patient-specific estimation of blood urea concentration. 32 patient samples of paired sweat and blood urea concentrations, collected both before and after HD, were used to validate the model.
RESULTS: This resulted in an excellent Pearson correlation coefficient (0.98, 95%CI: 0.95-0.99) and a clinically irrelevant bias (-0.181 mmol/L before and -0.005 mmol/L after HD).
DISCUSSION: This model enabled the accurate estimation of blood urea concentrations from sweat measurements. By accurately estimating blood urea concentrations from sweat measurements, our model enables non-invasive and more frequent assessments of dialysis adequacy in ESRD patients. This approach could facilitate home-based and patient-friendly dialysis management, enhancing patient comfort while enabling more personalized treatment across diverse clinical settings.