ReviewKidney3602025
The Pathologic Actions of Phosphate in CKD.
Review in Kidney360, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
6 citing papers in PubMed.
- Review
- Article
- Review
- Soft tissue accumulations of phosphate are not always associated with serum phosphate or with calcifications in mouse models of hyperphosphatemia.The Journal of physiology · 2025Article
- Soft tissue calcifications in chronic kidney disease-beyond the vasculature.Pflugers Archiv : European journal of physiology · 2025Review
- Sex-specific differences in serum phosphate persist in patients with CKD.Jornal brasileiro de nefrologiaArticle
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
Abstract
CKD is associated with high serum levels of phosphate (also called hyperphosphatemia), which is a main driver of soft tissue calcifications and potentially other pathologic changes that are associated with CKD. However, it remains unclear in what form and through which mechanisms and targets elevated phosphate can damage cells and tissues. Rises in serum phosphate levels are accompanied by changes in the endocrine regulators of phosphate metabolism and result in the formation of calcium-phosphate crystals, and all three events can have pathologic actions on various tissues. Furthermore, tissues can accumulate phosphate from the circulation, and cells can generate free phosphate in their environment independently from circulating phosphate, which both result in local elevations of phosphate that could also contribute to tissue damage. It is important to better understand the various scenarios underlying the pathologic actions of hyperphosphatemia, as some of them suggest that measuring extracellular serum phosphate, which is the gold standard to estimate overall phosphate status of the body, is not sufficient to do so. Understanding the pathologic actions of phosphate on a conceptual level should not only help to design more efficient detection tools for phosphate but also to identify phosphate-induced pathomechanisms which could provide us with novel drug targets to tackle phosphate-driven pathologies in CKD. Here, we discuss the different concepts and scenarios that could underlie the widespread pathologic actions of hyperphosphatemia in CKD.
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What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.