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慢性肾脏病中磷酸盐的血管毒性:超越血管钙化

Vascular toxicity of phosphate in chronic kidney disease: beyond vascular calcification .

作者信息

Gross Priscilla, Six Isabelle, Kamel Said, Massy Ziad A

机构信息

INSERM Unit 1088, Jules Verne University of Picardie.

出版信息

Circ J. 2014;78(10):2339-46. doi: 10.1253/circj.cj-14-0735. Epub 2014 Jul 31.

Abstract

Chronic kidney disease (CKD) is characterized by high cardiovascular morbidity/mortality, which is linked in part to vascular calcification (VC) and endothelial dysfunction (ED). Hyperphosphatemia, a feature of CKD, is a well-known inducer of VC in preclinical models and is associated with poor outcomes in epidemiological studies. However, it remains to be seen whether lowering phosphate levels in CKD patients reduces VC and the morbidity/mortality rate. Furthermore, it is now clear from preclinical and clinical studies that phosphate is involved in ED. The present article reviews the direct and indirect mechanisms (eg, via fibroblast growth factor 23 and/or parathyroid hormone) by which hyperphosphatemia influence the onset of VC and ED in CKD.

摘要

慢性肾脏病(CKD)的特征是心血管疾病的高发病率/死亡率,这部分与血管钙化(VC)和内皮功能障碍(ED)有关。高磷血症是CKD的一个特征,在临床前模型中是众所周知的VC诱导因素,并且在流行病学研究中与不良预后相关。然而,降低CKD患者的磷酸盐水平是否能降低VC和发病率/死亡率仍有待观察。此外,临床前和临床研究现已明确表明磷酸盐与ED有关。本文综述了高磷血症通过直接和间接机制(如通过成纤维细胞生长因子23和/或甲状旁腺激素)影响CKD中VC和ED发生的机制。

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