University Department of Nephrology, Faculty of Medicine, University of Medicine Tirana, Tirana 1001, Albania.
Institute of Anatomy, University of Zurich, 8057 Zurich, Switzerland.
Toxins (Basel). 2020 Feb 25;12(3):140. doi: 10.3390/toxins12030140.
Cardiovascular (CV) disease is highly prevalent in the population with chronic kidney disease (CKD), where the risk of CV death in early stages far exceeds the risk of progression to dialysis. The presence of chronic kidney disease-mineral and bone disorder (CKD-MBD) has shown a strong correlation with CV events and mortality. As a non-atheromatous process, it could be partially explained why standard CV disease-modifying drugs do not provide such an impact on CV mortality in CKD as observed in the general population. We summarize the potential association of CV comorbidities with the older (parathyroid hormone, phosphate) and newer (FGF23, Klotho, sclerostin) CKD-MBD biomarkers.
心血管疾病在患有慢性肾脏病(CKD)的人群中非常普遍,在早期阶段,心血管死亡的风险远远超过进展为透析的风险。慢性肾脏病-矿物质和骨异常(CKD-MBD)的存在与心血管事件和死亡率有很强的相关性。作为一种非动脉粥样硬化过程,这部分可以解释为什么标准的心血管疾病修饰药物对 CKD 患者的心血管死亡率没有像在普通人群中那样产生影响。我们总结了心血管合并症与较老(甲状旁腺激素、磷酸盐)和较新(FGF23、Klotho、骨硬化蛋白)的 CKD-MBD 生物标志物之间的潜在关联。