Koumakis Eugénie, Cormier Catherine, Roux Christian, Briot Karine
Reference Center for Rare Disorders of Calcium and Phosphate Metabolism, Reference Center for Rare Genetic Bone Disorders, OSCAR Filière, Rheumatology Department, Cochin Hospital, AP-HP Centre-Paris University, 27 Rue du Faubourg Saint-Jacques, 75014, Paris, France.
Calcif Tissue Int. 2021 Jan;108(1):41-73. doi: 10.1007/s00223-020-00664-9. Epub 2020 Apr 13.
Phosphate homeostasis involves several major organs that are the skeleton, the intestine, the kidney, and parathyroid glands. Major regulators of phosphate homeostasis are parathormone, fibroblast growth factor 23, 1,25-dihydroxyvitamin D, which respond to variations of serum phosphate levels and act to increase or decrease intestinal absorption and renal tubular reabsorption, through the modulation of expression of transcellular transporters at the intestinal and/or renal tubular level. Any acquired or genetic dysfunction in these major organs or regulators may induce hypo- or hyperphosphatemia. The causes of hypo- and hyperphosphatemia are numerous. This review develops the main causes of acquired and genetic hypo- and hyperphosphatemia.
磷稳态涉及多个主要器官,即骨骼、肠道、肾脏和甲状旁腺。磷稳态的主要调节因子是甲状旁腺激素、成纤维细胞生长因子23、1,25 - 二羟维生素D,它们对血清磷水平的变化做出反应,并通过调节肠道和/或肾小管水平的跨细胞转运体的表达,来增加或减少肠道吸收和肾小管重吸收。这些主要器官或调节因子中的任何获得性或遗传性功能障碍都可能导致低磷血症或高磷血症。低磷血症和高磷血症的病因众多。本综述阐述了获得性和遗传性低磷血症及高磷血症的主要病因。