Evidence map›Paper›PMID 40097533›Full record

ArticleScientific reports2025

Mathematical models for phosphate kinetics in patients on maintenance hemodialysis.

Jacek Waniewski, Malgorzata Debowska, Alicja Wojcik-Zaluska, Wojciech Zaluska, Bengt Lindholm

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In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Jacek WaniewskiNalecz Institute of Biocybernetics and Biomedical Engineering, Polish Academy of Sciences, Warsaw, Poland.
Malgorzata DebowskaNalecz Institute of Biocybernetics and Biomedical Engineering, Polish Academy of Sciences, Warsaw, Poland. mdebowska@ibib.waw.pl.
Alicja Wojcik-ZaluskaDepartment of Clinical Physiotherapy, Medical University of Lublin, Lublin, Poland.
Wojciech ZaluskaDepartment of Nephrology, Medical University of Lublin, Lublin, Poland.
Bengt LindholmRenal Medicine and Baxter Novum, Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

Models, BiologicalModels, TheoreticalPhosphatesRenal DialysisHumansHyperphosphatemiaKineticsPhosphatesChronic kidney diseaseIntracellular phosphate storesKinetics of hemodialysisMineral metabolism

Identifiers

PMID40097533
PMCPMC11914670

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