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Prescribed dietary phosphate restriction and survival among hemodialysis patients.透析患者的规定饮食磷酸盐限制与生存。
Clin J Am Soc Nephrol. 2011 Mar;6(3):620-9. doi: 10.2215/CJN.04620510. Epub 2010 Dec 9.
2
Low socioeconomic status associates with higher serum phosphate irrespective of race.低社会经济地位与血清磷酸盐升高有关,而与种族无关。
J Am Soc Nephrol. 2010 Nov;21(11):1953-60. doi: 10.1681/ASN.2010020221. Epub 2010 Sep 16.
3
Pilot study of dietary phosphorus restriction and phosphorus binders to target fibroblast growth factor 23 in patients with chronic kidney disease.慢性肾脏病患者饮食磷限制和磷结合剂靶向成纤维细胞生长因子 23 的初步研究。
Nephrol Dial Transplant. 2011 Feb;26(2):584-91. doi: 10.1093/ndt/gfq419. Epub 2010 Jul 14.
4
Forging forward with 10 burning questions on FGF23 in kidney disease.在肾病中探索成纤维细胞生长因子 23(FGF23)的 10 大热点问题。
J Am Soc Nephrol. 2010 Sep;21(9):1427-35. doi: 10.1681/ASN.2009121293. Epub 2010 May 27.
5
Fibroblast growth factor-23 in early chronic kidney disease: additional support in favor of a phosphate-centric paradigm for the pathogenesis of secondary hyperparathyroidism.成纤维细胞生长因子 23 在慢性肾脏病早期:对继发性甲状旁腺功能亢进发病机制的磷中心假说提供更多支持。
Clin J Am Soc Nephrol. 2010 Jul;5(7):1268-76. doi: 10.2215/CJN.08241109. Epub 2010 May 6.
6
Association of dietary phosphorus intake and phosphorus to protein ratio with mortality in hemodialysis patients.饮食磷摄入量和磷与蛋白比值与血液透析患者死亡率的关系。
Clin J Am Soc Nephrol. 2010 Apr;5(4):683-92. doi: 10.2215/CJN.08601209. Epub 2010 Feb 25.
7
Understanding sources of dietary phosphorus in the treatment of patients with chronic kidney disease.了解慢性肾脏病患者治疗中饮食磷的来源。
Clin J Am Soc Nephrol. 2010 Mar;5(3):519-30. doi: 10.2215/CJN.06080809. Epub 2010 Jan 21.
8
KDIGO clinical practice guideline for the diagnosis, evaluation, prevention, and treatment of Chronic Kidney Disease-Mineral and Bone Disorder (CKD-MBD).改善全球肾脏病预后组织(KDIGO)慢性肾脏病-矿物质和骨异常(CKD-MBD)诊断、评估、预防及治疗临床实践指南。
Kidney Int Suppl. 2009 Aug(113):S1-130. doi: 10.1038/ki.2009.188.
9
A randomized double-blind pilot study of serum phosphorus normalization in chronic kidney disease: a new paradigm for clinical outcomes studies in nephrology.一项慢性肾脏病血清磷正常化的随机双盲试点研究:肾脏病临床结局研究的新范式
Hemodial Int. 2009 Jul;13(3):360-2. doi: 10.1111/j.1542-4758.2009.00387.x. Epub 2009 Jul 7.
10
Effect of food additives on hyperphosphatemia among patients with end-stage renal disease: a randomized controlled trial.食品添加剂对终末期肾病患者高磷血症的影响:一项随机对照试验。
JAMA. 2009 Feb 11;301(6):629-35. doi: 10.1001/jama.2009.96.

慢性肾脏病3-5期的磷代谢:饮食与药物控制

Phosphate Metabolism in CKD Stages 3-5: Dietary and Pharmacological Control.

作者信息

Ketteler Markus

机构信息

Division of Nephrology, Klinikum Coburg, 96450 Coburg, Germany.

出版信息

Int J Nephrol. 2011;2011:970245. doi: 10.4061/2011/970245. Epub 2011 May 23.

DOI:10.4061/2011/970245
PMID:21660261
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3108253/
Abstract

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.

摘要

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。