Ketteler Markus
Division of Nephrology, Klinikum Coburg, 96450 Coburg, Germany.
Int J Nephrol. 2011;2011:970245. doi: 10.4061/2011/970245. Epub 2011 May 23.
When compared to the available information for patients on dialysis (CKD stage 5D), data on the epidemiology and appropriate treatment of calcium and phosphate metabolism in the predialysis stages of chronic kidney disease (CKD) are quite limited. Perceptible derangements of calcium and phosphate levels start to become apparent when GFR falls below 30 mL/min in some, but not all, patients. However, hyperphosphatemia may be a significant morbidity and mortality risk predictor in predialysis CKD stages. The RIND study, evaluating progression of coronary artery calcification in incident hemodialysis patients, indirectly demonstrated that vascular calcification processes start to manifest in CKD patients prior to the dialysis stage, which may be closely linked to early and invisible derangements in calcium and phosphate homeostasis. Novel insights into the pathophysiology of calcium and phosphate handling such as the discovery of FGF23 and other phosphatonins suggest that a more complex assessment of phosphate balance is warranted, possibly including measurements of fractional phosphate excretion and phosphatonin levels in order to appropriately evaluate disordered metabolism in earlier stages of kidney disease. As a consequence, early and preventive treatment approaches may have to be developed for patients in CKD stages 3-5 to halt progression of CKD-MBD.
与透析患者(慢性肾脏病5D期)的现有信息相比,慢性肾脏病(CKD)透析前阶段钙磷代谢的流行病学和适当治疗的数据相当有限。在一些(但不是所有)患者中,当肾小球滤过率(GFR)降至30 mL/min以下时,钙磷水平的明显紊乱开始变得明显。然而,高磷血症可能是透析前CKD阶段发病率和死亡率的重要风险预测指标。RIND研究评估了初发血液透析患者冠状动脉钙化的进展,间接表明血管钙化过程在透析阶段之前就开始在CKD患者中显现,这可能与钙磷稳态的早期和隐匿性紊乱密切相关。对钙磷处理病理生理学的新见解,如成纤维细胞生长因子23(FGF23)和其他磷调节素的发现,表明有必要对磷平衡进行更复杂的评估,可能包括测量磷排泄分数和磷调节素水平,以便在肾脏疾病的早期阶段适当地评估代谢紊乱。因此,可能必须为CKD 3 - 5期患者制定早期和预防性治疗方法,以阻止慢性肾脏病-矿物质和骨异常(CKD-MBD)的进展。