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Phosphate Metabolism: From Physiology to Toxicity
1Department of Pathology, Lake Erie College of Osteopathic Medicine, Erie, PA, USA. mrazzaque@lecom.edu.
Systemic phosphate homeostasis is regulated by organ interactions and hormones like FGF23, vitamin D, and PTH. This book details the complex physiologic and pathologic regulation of phosphate metabolism.
Area of Science:
- Physiology
- Endocrinology
- Nephrology
Background:
- Systemic phosphate homeostasis is a complex process involving multiple organs: intestine, kidney, bone, and parathyroid glands.
- Fibroblast growth factor 23 (FGF23), vitamin D, and parathyroid hormone (PTH) are key endocrine regulators of phosphate balance.
- FGF23, in conjunction with klotho, modulates kidney sodium-phosphate (NaPi) co-transporters, influencing systemic phosphate levels.
Purpose of the Study:
- To provide a comprehensive overview of the physiologic regulation of phosphate homeostasis.
- To elucidate the pathologic dysregulation of phosphate in various health and disease states.
- To serve as a reference for updated information on phosphate metabolism.
Main Methods:
- This work is a curated collection of chapters organized by the editor.
- It synthesizes current knowledge on phosphate metabolism.
- Focuses on the interplay of hormones and organs in phosphate balance.
Main Results:
- The book details the intricate cross-organ communication essential for phosphate homeostasis.
- It explains the molecular mechanisms, including FGF23-klotho signaling, affecting kidney phosphate handling.
- Information on both normal physiological regulation and disease-associated dysregulation is presented.
Conclusions:
- Understanding phosphate homeostasis requires knowledge of endocrine factors and organ crosstalk.
- This volume offers accessible insights into phosphate metabolism for a broad audience.
- It serves as a valuable resource for researchers and clinicians interested in phosphate regulation.
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