Atherosclerosis in Chronic Kidney Disease.

J. Valdivielso, D. Rodríguez‐Puyol, J. Pascual, C. Barrios, M. Bermúdez-López, M. Sánchez-Niño, M. Pérez-Fernández, A. Ortiz
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引用次数: 84

Abstract

Patients with chronic kidney disease (CKD) are at an increased risk of premature mortality, mainly from cardiovascular causes. The association between CKD on hemodialysis and accelerated atherosclerosis was described >40 years ago. However, more recently, it has been suggested that the increase in atherosclerosis risk is actually observed in early CKD stages, remaining stable thereafter. In this regard, interventions targeting the pathogenesis of atherosclerosis, such as statins, successful in the general population, have failed to benefit patients with very advanced CKD. This raises the issue of the relative contribution of atherosclerosis versus other forms of cardiovascular injury such as arteriosclerosis or myocardial injury to the increased cardiovascular risk in CKD. In this review, the pathophysiogical contributors to atherosclerosis in CKD that are shared with the general population, or specific to CKD, are discussed. The NEFRONA study prospectively assessed the prevalence and progression of subclinical atherosclerosis (plaque in vascular ultrasound), confirming an increased prevalence of atherosclerosis in patients with moderate CKD. However, the adjusted odds ratio for subclinical atherosclerosis increased with CKD stage, suggesting a contribution of CKD itself to subclinical atherosclerosis. Progression of atherosclerosis was closely related to CKD progression as well as to the baseline presence of atheroma plaque, and to higher phosphate, uric acid, and ferritin and lower 25(OH) vitamin D levels. These insights may help design future clinical trials of stratified personalized medicine targeting atherosclerosis in patients with CKD. Future primary prevention trials should enroll patients with evidence of subclinical atherosclerosis and should provide a comprehensive control of all known risk factors in addition to testing any additional intervention or placebo.
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慢性肾脏疾病中的动脉粥样硬化。
慢性肾脏疾病(CKD)患者的过早死亡风险增加,主要是由心血管原因引起的。血液透析导致的CKD与动脉粥样硬化加速之间的关系早在40年前就有报道。然而,最近有研究表明,动脉粥样硬化风险的增加实际上是在早期CKD阶段观察到的,此后保持稳定。在这方面,针对动脉粥样硬化发病机制的干预措施,如他汀类药物,在普通人群中成功,但未能使非常晚期的CKD患者受益。这就提出了动脉粥样硬化与其他形式的心血管损伤(如动脉硬化或心肌损伤)对CKD心血管风险增加的相对贡献的问题。在这篇综述中,讨论了CKD中动脉粥样硬化的病理生理因素,这些因素与一般人群共享,或特定于CKD。NEFRONA研究前瞻性地评估了亚临床动脉粥样硬化(血管超声斑块)的患病率和进展,证实了中度CKD患者动脉粥样硬化的患病率增加。然而,调整后的亚临床动脉粥样硬化的优势比随着CKD分期的增加而增加,这表明CKD本身对亚临床动脉粥样硬化有贡献。动脉粥样硬化的进展与CKD的进展、动脉粥样硬化斑块的基线存在、较高的磷酸盐、尿酸和铁蛋白以及较低的25(OH)维生素D水平密切相关。这些见解可能有助于设计针对CKD患者动脉粥样硬化的分层个性化药物的未来临床试验。未来的一级预防试验应纳入有亚临床动脉粥样硬化证据的患者,除了测试任何额外的干预措施或安慰剂外,还应提供所有已知危险因素的全面控制。
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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Editors and Editorial Board. Correction to: Role of LpL (Lipoprotein Lipase) in Macrophage Polarization In Vitro and In Vivo. Tribute to Paul M. Vanhoutte, MD, PhD (1940-2019). Correction to: 18F-Sodium Fluoride Imaging of Coronary Atherosclerosis in Ambulatory Patients With Diabetes Mellitus. Extracellular MicroRNA-92a Mediates Endothelial Cell-Macrophage Communication.
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