» Articles » PMID: 31505780

Modifying Phosphate Toxicity in Chronic Kidney Disease

Overview
Journal Toxins (Basel)
Publisher MDPI
Specialty Toxicology
Date 2019 Sep 12
PMID 31505780
Citations 8
Authors
Affiliations
Soon will be listed here.
Abstract

Phosphate toxicity is a well-established phenomenon, especially in chronic kidney disease (CKD), where hyperphosphatemia is a frequent occurrence when CKD is advanced. Many therapeutic efforts are targeted at phosphate, and comprise dietary intervention, modifying dialysis schemes, treating uncontrolled hyperparathyroidism and importantly, phosphate binder therapy. Despite all these interventions, hyperphosphatemia persists in many, and its pathological influence is ongoing. In nephrological care, a somewhat neglected aspect of treatment-when attempts fail to lower exposure to a toxin like phosphate-is to explore the possibility of "anti-dotes". Indeed, quite a long list of factors modify, or are mediators of phosphate toxicity. Addressing these, especially when phosphate itself cannot be sufficiently controlled, may provide additional protection. In this narrative overview, several factors are discussed that may qualify as either such a modifier or mediator, that can be influenced by other means than simply lowering phosphate exposure. A wider scope when targeting phosphate-induced comorbidity in CKD, in particular cardiovascular disease, may alleviate the burden of disease that is the consequence of this potentially toxic mineral in CKD.

Citing Articles

Minerals and Human Health: From Deficiency to Toxicity.

Razzaque M, Wimalawansa S Nutrients. 2025; 17(3).

PMID: 39940312 PMC: 11820417. DOI: 10.3390/nu17030454.


Phosphorus: Chronicles of the epistemology of a vital element.

Eknoyan G, Lederer E Clin Nephrol. 2024; 102(3):117-124.

PMID: 38836367 PMC: 11370277. DOI: 10.5414/CN111435.


Redefying the therapeutic strategies against cardiorenal morbidity and mortality: Patient phenotypes.

Bacharaki D, Petrakis I, Stylianou K World J Cardiol. 2023; 15(3):76-83.

PMID: 37033683 PMC: 10074996. DOI: 10.4330/wjc.v15.i3.76.


Phosphate Homeostasis and Disorders of Phosphate Metabolism.

Perumal N, Padidela R Curr Pediatr Rev. 2022; 20(4):412-425.

PMID: 36545737 DOI: 10.2174/1573396319666221221121350.


Circulating -Cresyl Sulfate, Non-Hepatic Alkaline Phosphatase and Risk of Bone Fracture Events in Chronic Kidney Disease-Mineral Bone Disease.

Chang J, Hsieh C, Liou J, Lu K, Zheng C, Wu M Toxins (Basel). 2021; 13(7).

PMID: 34357951 PMC: 8310177. DOI: 10.3390/toxins13070479.


References
1.
Hugtenburg J, Timmers L, Elders P, Vervloet M, van Dijk L . Definitions, variants, and causes of nonadherence with medication: a challenge for tailored interventions. Patient Prefer Adherence. 2013; 7:675-82. PMC: 3711878. DOI: 10.2147/PPA.S29549. View

2.
Cranenburg E, Vermeer C, Koos R, Boumans M, Hackeng T, Bouwman F . The circulating inactive form of matrix Gla Protein (ucMGP) as a biomarker for cardiovascular calcification. J Vasc Res. 2008; 45(5):427-36. DOI: 10.1159/000124863. View

3.
Scialla J, Xie H, Rahman M, Anderson A, Isakova T, Ojo A . Fibroblast growth factor-23 and cardiovascular events in CKD. J Am Soc Nephrol. 2013; 25(2):349-60. PMC: 3904568. DOI: 10.1681/ASN.2013050465. View

4.
Jono S, McKee M, Murry C, Shioi A, Nishizawa Y, Mori K . Phosphate regulation of vascular smooth muscle cell calcification. Circ Res. 2000; 87(7):E10-7. DOI: 10.1161/01.res.87.7.e10. View

5.
Insogna K, Briot K, Imel E, Kamenicky P, Ruppe M, Portale A . A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Trial Evaluating the Efficacy of Burosumab, an Anti-FGF23 Antibody, in Adults With X-Linked Hypophosphatemia: Week 24 Primary Analysis. J Bone Miner Res. 2018; 33(8):1383-1393. DOI: 10.1002/jbmr.3475. View