Kovesdy Csaba P, Kalantar-Zadeh Kamyar
Division of Nephrology, Salem VA Medical Center, 1970 Roanoke Boulevard, Salem, VA 24153, USA.
Int Urol Nephrol. 2008;40(2):427-40. doi: 10.1007/s11255-008-9346-7.
Disorders in calcium, phosphorus, and parathyroid hormone (PTH) are common in chronic kidney disease (CKD) and may be associated with poor outcomes including a higher rate of CKD progression and increased death risk. Although these abnormalities have been examined extensively in patients with CKD stage 5 who are receiving chronic maintenance dialysis, they have not been studied to the same extent at earlier stages of CKD, in spite of the much larger numbers of patients in the early CKD population. We summarize the available literature on outcomes associated with bone and mineral disorders in patients with CKD not yet receiving maintenance dialysis. We have reviewed novel data linking fibroblast growth factor 23 (FGF-23) to phosphorus and vitamin D homeostasis. More rapid CKD progression is linked to hyperphosphatemia and its associated hyperparathyroidism and vitamin D deficiency. Hence, hyperphosphatemia may play a central role in the diverse disorders characterizing CKD. We provide a brief overview of the available treatment recommendations for bone and mineral disorders, with an emphasis on areas needing further research.
钙、磷及甲状旁腺激素(PTH)紊乱在慢性肾脏病(CKD)中很常见,可能与不良预后相关,包括CKD进展加快和死亡风险增加。尽管这些异常情况在接受慢性维持性透析的CKD 5期患者中已得到广泛研究,但在CKD早期阶段,尽管早期CKD患者数量更多,却未得到同样程度的研究。我们总结了尚未接受维持性透析的CKD患者中与骨和矿物质紊乱相关的现有文献。我们回顾了将成纤维细胞生长因子23(FGF - 23)与磷及维生素D稳态联系起来的新数据。更快的CKD进展与高磷血症及其相关的甲状旁腺功能亢进和维生素D缺乏有关。因此,高磷血症可能在CKD的各种紊乱中起核心作用。我们简要概述了骨和矿物质紊乱的现有治疗建议,重点关注需要进一步研究的领域。