Recent Advances in the Management of Vascular Calcification in Patients with End-Stage Renal Disease.

4区 医学 Q3 Medicine Contributions to nephrology Pub Date : 2019-01-01 Epub Date: 2019-04-16 DOI:10.1159/000496532
Kosaku Nitta, Tetsuya Ogawa, Norio Hanafusa, Ken Tsuchiya
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引用次数: 14

Abstract

Background: Vascular calcification (VC) is common in patients with chronic kidney disease (CKD) including end-stage renal disease (ESRD). The pathogenesis of VC is complex, resulting in increased arterial stiffening, which is associated with cardiovascular mortality. In addition to traditional cardiovascular risk factors, CKD patients also have a number of non-traditional cardiovascular risk factors that may play an important role in the pathogenesis of VC.

Summary: Management of CKD-mineral bone disorder using conventional therapeutic approaches, which include restricting dietary phosphate, administering phosphate binders, and using active vitamin D and calcimimetics, may inhibit the progression of VC, but these approaches remain controversial because recommended biochemical targets are difficult to achieve. Current treatment strategies focus on correcting abnormal calcium, phosphate, parathyroid hormone, and vitamin D levels in ESRD patients. Novel therapies for addressing VC include magnesium and vitamin K supplementation, which are currently being investigated in randomized controlled trials. This review summarizes current treatment strategies and therapeutic targets for the management of VC in patients with ESRD. Key Messages: A better understanding of the potential therapeutic approaches to VC may lead to improved mortality rates among patients with CKD including those on dialysis. Fetuin-A inhibits VC by binding to the nanoparticles of calcium and phosphate, preventing mineral accretion. These particles are known as calciprotein particles and may provide an important pathway for mineral transport and clearance. This review article summarizes the current management of VC in patients with ESRD.

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终末期肾病患者血管钙化处理的最新进展。
背景:血管钙化(VC)在包括终末期肾病(ESRD)在内的慢性肾脏疾病(CKD)患者中很常见。VC的发病机制是复杂的,可导致动脉硬化增加,这与心血管死亡率有关。除了传统的心血管危险因素外,CKD患者还有一些非传统的心血管危险因素,这些因素可能在VC的发病过程中起重要作用。摘要:使用传统的治疗方法,包括限制饮食中的磷酸盐,给予磷酸盐结合剂,使用活性维生素D和石灰化剂,可以抑制VC的进展,但这些方法仍然存在争议,因为推荐的生化指标难以实现。目前的治疗策略侧重于纠正ESRD患者异常的钙、磷酸盐、甲状旁腺激素和维生素D水平。解决VC的新疗法包括补充镁和维生素K,目前正在随机对照试验中进行研究。本文综述了ESRD患者VC管理的当前治疗策略和治疗靶点。关键信息:更好地了解VC的潜在治疗方法可能导致CKD患者包括透析患者死亡率的提高。Fetuin-A通过与钙和磷酸盐纳米颗粒结合抑制VC,防止矿物质积聚。这些颗粒被称为钙蛋白颗粒,可能为矿物质运输和清除提供了重要途径。本文综述了ESRD患者VC的管理现状。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Contributions to nephrology
Contributions to nephrology 医学-泌尿学与肾脏学
CiteScore
1.50
自引率
0.00%
发文量
0
审稿时长
6-12 weeks
期刊介绍: The speed of developments in nephrology has been fueled by the promise that new findings may improve the care of patients suffering from renal disease. Participating in these rapid advances, this series has released an exceptional number of volumes that explore problems of immediate importance for clinical nephrology. Focus ranges from discussion of innovative treatment strategies to critical evaluations of investigative methodology. The value of regularly consolidating the newest findings and theories is enhanced through the inclusion of extensive bibliographies which make each volume a reference work deserving careful study.
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