Phosphate balance during dialysis and after kidney transplantation in patients with chronic kidney disease

被引:2
|
作者
Duque, Eduardo J. [1 ]
Elias, Rosilene M. [1 ,2 ]
Moyses, Rosa M. A. [1 ]
机构
[1] Univ Sao Paulo, Lab Fisiopatol Renal LIM16, Hosp Clin HCFMUSP, Fac Med, Sao Paulo, Brazil
[2] Nove Julho Univ, Postgrad Program Med, Sao Paulo, SP, Brazil
来源
CURRENT OPINION IN NEPHROLOGY AND HYPERTENSION | 2022年 / 31卷 / 04期
关键词
chronic kidney disease-mineral and bone disorder; dialysis; hyperphosphatemia; mineral balance; phosphate; GROWTH-FACTOR; 23; CIRCADIAN-RHYTHM; CALCIUM; PHOSPHORUS; HEMODIALYSIS; TRANSPORT; HYPOPHOSPHATEMIA; RAPAMYCIN; REMOVAL; HYPERPHOSPHATONINISM;
D O I
10.1097/MNH.0000000000000802
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Purpose of review In patients with chronic kidney disease (CKD), hyperphosphatemia is associated with several adverse outcomes, including bone fragility and progression of kidney and cardiovascular disease. However, there is a knowledge gap regarding phosphate balance in CKD. This review explores its current state, depending on the stage of CKD, dialysis modalities, and the influence of kidney transplantation. Recent findings Adequate phosphate control is one of the goals of treatment for CKD-mineral and bone disorder. However, ongoing studies are challenging the benefits of phosphate-lowering treatment. Nevertheless, the current therapy is based on dietary restriction, phosphate binders, and optimal removal by dialysis. In the face of limited adherence, due to the high pill burden, adjuvant options are under investigation. The recent discovery that intestinal absorption of phosphate is mostly paracellular when the intraluminal concentration is adequate might help explain why phosphate is still well absorbed in CKD, despite the lower levels of calcitriol. Future studies could confirm the benefits of phosphate control. Greater understanding of the complex distribution of phosphate among the body compartments will help us define a better therapeutic strategy in patients with CKD.
引用
收藏
页码:326 / 331
页数:6
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