Modifying Phosphate Toxicity in Chronic Kidney Disease

被引:18
作者
Vervloet, Marc [1 ]
机构
[1] Univ Amsterdam, Med Ctr, Dept Nephrol & Amsterdam Cardiovasc Sci, Boelelaan 1117, NL-1081 HV Amsterdam, Netherlands
关键词
chronic kidney disease; CKD-MBD; phosphate; MATRIX GLA-PROTEIN; CORONARY-ARTERY CALCIFICATION; FIBROBLAST GROWTH FACTOR-23; VITAMIN-K SUPPLEMENTATION; CONTAINING CALCIPROTEIN PARTICLES; AORTIC-VALVE CALCIFICATION; SOFT-TISSUE CALCIFICATION; SMOOTH-MUSCLE-CELLS; VASCULAR CALCIFICATION; FETUIN-A;
D O I
10.3390/toxins11090522
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Phosphate toxicity is a well-established phenomenon, especially in chronic kidney disease (CKD), where hyperphosphatemia is a frequent occurrence when CKD is advanced. Many therapeutic efforts are targeted at phosphate, and comprise dietary intervention, modifying dialysis schemes, treating uncontrolled hyperparathyroidism and importantly, phosphate binder therapy. Despite all these interventions, hyperphosphatemia persists in many, and its pathological influence is ongoing. In nephrological care, a somewhat neglected aspect of treatment-when attempts fail to lower exposure to a toxin like phosphate-is to explore the possibility of "anti-dotes". Indeed, quite a long list of factors modify, or are mediators of phosphate toxicity. Addressing these, especially when phosphate itself cannot be sufficiently controlled, may provide additional protection. In this narrative overview, several factors are discussed that may qualify as either such a modifier or mediator, that can be influenced by other means than simply lowering phosphate exposure. A wider scope when targeting phosphate-induced comorbidity in CKD, in particular cardiovascular disease, may alleviate the burden of disease that is the consequence of this potentially toxic mineral in CKD.
引用
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页数:17
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