Waniewski Jacek, Debowska Malgorzata, Wojcik-Zaluska Alicja, Zaluska Wojciech, Lindholm Bengt
Nalecz Institute of Biocybernetics and Biomedical Engineering, Polish Academy of Sciences, Warsaw, Poland.
Department of Clinical Physiotherapy, Medical University of Lublin, Lublin, Poland.
Sci Rep. 2025 Mar 17;15(1):9176. doi: 10.1038/s41598-025-93443-1.
In maintenance hemodialysis patients, efficient removal of phosphate during the hemodialysis session is crucial for the control of hyperphosphatemia and other frequent abnormalities of mineral metabolism. A mathematical model that integrates different distribution compartments and forms of phosphate may provide deeper insight and elucidation of observed kinetics of phosphate levels in plasma. Three mathematical models were constructed to describe the kinetics of phosphate during a one-week cycle of three dialysis sessions. The models included the extracellular and intracellular compartments for phosphate ions, plasma and interstitial compartments for phosphate ions bound to protein, and a compartment for fast exchangeable phosphate ions, and differing by the presence or exclusion of the fast or the intracellular compartment. The models included also an intracellular store of phosphate that might be released at an increasing rate during dialysis sessions. The weekly kinetics of total phosphate levels in plasma predicted by the three models were similar and agreed with the clinical data. The inclusion of free phosphate ion and protein bound phosphate separately provided small but significant modifications of the predicted profiles. The time dependent release of phosphate from the intracellular store was critical for the correct description of phosphate kinetics in plasma. The hypothesis that a fast compartment and an intracellular store compartment separately or combined contribute significantly to the kinetics of total phosphate in plasma was shown to be compatible with clinical data.
在维持性血液透析患者中,血液透析期间有效清除磷酸盐对于控制高磷血症和其他常见的矿物质代谢异常至关重要。一个整合了不同分布区室和磷酸盐形式的数学模型可能会为观察到的血浆中磷酸盐水平的动力学提供更深入的见解和阐释。构建了三个数学模型来描述在为期一周的三个透析疗程周期内磷酸盐的动力学。这些模型包括磷酸盐离子的细胞外和细胞内区室、与蛋白质结合的磷酸盐离子的血浆和间质区室,以及一个快速可交换磷酸盐离子区室,并且因快速或细胞内区室的存在或排除而有所不同。这些模型还包括一个磷酸盐的细胞内储存库,其可能在透析疗程期间以递增速率释放。这三个模型预测的血浆中总磷酸盐水平的每周动力学相似且与临床数据相符。分别纳入游离磷酸盐离子和与蛋白质结合的磷酸盐对预测曲线有微小但显著的修正。磷酸盐从细胞内储存库的时间依赖性释放对于正确描述血浆中的磷酸盐动力学至关重要。快速区室和细胞内储存区室单独或联合对血浆中总磷酸盐动力学有显著贡献这一假设被证明与临床数据相符。