Primary Disorders of Phosphate Metabolism

Review
In: Endotext [Internet]. South Dartmouth (MA): MDText.com, Inc.; 2000.
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Excerpt

Phosphorus is critical to many functions in human biology. Deprivation of phosphorus may manifest as disorders of the musculoskeletal system, reflecting its important role in energy metabolism and skeletal mineralization. Phosphorus excess can promote heterotopic mineralization and is associated with mortality, particularly in the setting of chronic kidney disease. Inorganic phosphorus, primarily occurring as phosphate (PO4), is highly regulated by transport systems in intestine and kidney, and is essential for the formation of a mineralized skeleton. Parathyroid hormone (PTH) and Fibroblast Growth Factor 23 (FGF23) are major hormonal regulators of phosphate homeostasis and membrane abundance of PO4 transporters. Tissue distribution of alpha-klotho permits a primary renal specificity for FGF23 actions. Disorders of phosphate metabolism that are encountered in clinical practice are described in this Endotext chapter, with an emphasis on pathophysiologic processes, diagnostic measures, and treatment. The identification of FGF23 as an important mediator of phosphate homeostasis has brought to light the underlying disease processes in many of these conditions, along with the possibility of novel, physiologic-based therapies. For complete coverage of all related areas of Endocrinology, please visit our on-line FREE web-text, WWW.ENDOTEXT.ORG.

Publication types

  • Review