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FGF-23: the rise of a novel cardiovascular risk marker in CKD

机译:FGF-23:CKD中新型心血管危险标志物的兴起

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摘要

Elevated plasma levels of the phosphaturic hormone fibroblast growth factor 23 (FGF-23) are a hallmark of chronic kidney disease (CKD)-mineral and bone disorder. FGF-23 allows serum phosphate levels within physiological limits to be maintained in progressive CKD until end-stage renal disease is reached. Despite its seemingly beneficial role in phosphate homeostasis, several prospective studies in dialysis patients and in patients with less advanced CKD associated elevated FGF-23 with poor cardiovascular and renal outcome. Moreover, very recent evidence suggests an adverse prognostic impact of elevated FGF-23 even in subjects without manifest CKD. These epidemiological data are supplemented by laboratory findings that reveal a pathophysiological role of FGF-23 in the pathogenesis of myocardial injury. In aggregate, these clinical and experimental data identify FGF-23 as a promising target of novel therapeutic interventions in CKD and beyond, which should be tested in future clinical trials.
机译:血浆磷脂酰激素成纤维细胞生长因子23(FGF-23)升高是慢性肾脏疾病(CKD)-矿物质和骨骼疾病的标志。 FGF-23可在进行性CKD中将血清磷酸盐水平维持在生理范围内,直至达到晚期肾脏疾病。尽管它在磷酸盐体内平衡中具有看似有益的作用,但在透析患者和CKD晚期患者中的一些前瞻性研究与FGF-23升高相关,心血管和肾脏预后不良。而且,最近的证据表明,即使在没有明显CKD的受试者中,FGF-23升高也会对预后产生不利影响。这些流行病学数据得到了实验室发现的补充,这些发现揭示了FGF-23在心肌损伤的发病机理中的病理生理作用。总的来说,这些临床和实验数据表明FGF-23是CKD及以后的新型治疗手段的有希望的靶标,应在以后的临床试验中进行测试。

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