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The Importance of Phosphate Control in Chronic Kidney Disease
1Department of Blood Purification, Tokyo Women's Medical University, Tokyo 162-8666, Japan.
Insights
Chronic kidney disease-mineral bone disease (CKD-MBD) involves complex mineral imbalances. This review emphasizes phosphorus
Area of Science:
- Nephrology
- Endocrinology
- Mineral Metabolism
Background:
- Chronic kidney disease-mineral bone disease (CKD-MBD) encompasses osteopathy, abnormal serum data, and vascular calcification.
- Emerging factors like αKlotho and fibroblast growth factor 23 (FGF23) are clarifying CKD-MBD pathophysiology.
- Phosphate's role in CKD-MBD complications and outcomes is gaining significant attention over calcium and parathyroid hormone.
Purpose of the Study:
- To review CKD-MBD focusing on phosphorus' role.
- To explore phosphorus' involvement in CKD-MBD pathophysiology and complications.
- To discuss evidence-based therapeutic approaches for phosphorus management in CKD-MBD.
Main Methods:
- Literature review of existing clinical evidence.
- Analysis of the pathophysiology of CKD-MBD with emphasis on FGF23 and αKlotho.
- Synthesis of current understanding of phosphorus metabolism in chronic kidney disease.
Main Results:
- Phosphate metabolism and hyperphosphatemia are central to CKD-MBD.
- FGF23 and αKlotho play pivotal roles in phosphate regulation.
- Phosphate management is crucial for improving outcomes in CKD-MBD.
Conclusions:
- Phosphorus management is critical for addressing CKD-MBD.
- Understanding phosphorus' role is key to effective clinical treatment.
- This review highlights the importance of phosphorus in CKD-MBD pathophysiology and management.
Abstract:
A series of problems including osteopathy, abnormal serum data, and vascular calcification associated with chronic kidney disease (CKD) are now collectively called CKD-mineral bone disease (CKD-MBD). The pathophysiology of CKD-MBD is becoming clear with the emerging of αKlotho, originally identified as a progeria-causing protein, and bone-derived phosphaturic fibroblast growth factor 23 (FGF23) as associated factors. Meanwhile, compared with calcium and parathyroid hormone, which have long been linked with CKD-MBD, phosphate is now attracting more attention because of its association with complications and outcomes. Incidentally, as the pivotal roles of FGF23 and αKlotho in phosphate metabolism have been unveiled, how phosphate metabolism and hyperphosphatemia are involved in CKD-MBD and how they can be clinically treated have become of great interest. Thus, the aim of this review is reconsider CKD-MBD from the viewpoint of phosphorus, its involvement in the pathophysiology, causing complications, therapeutic approach based on the clinical evidence, and clarifying the importance of phosphorus management.
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