Mahmood Usman, Johnson David W, Fahim Magid A
Department of Nephrology, Princess Alexandra Hospital, Australia.
Australasian Kidney Trials Network, School of Medicine, University of Queensland, Brisbane, Australia.
AIMS Genet. 2016 Dec 26;4(1):1-20. doi: 10.3934/genet.2017.1.1. eCollection 2017.
Cardiovascular disease is the major cause of death, accounting for approximately 40 percent of all-cause mortality in patients receiving either hemodialysis or peritoneal dialysis. Cardiovascular risk stratification is an important aspect of managing dialysis patients as it enables early identification of high-risk patients, so therapeutic interventions can be optimized to lower cardiovascular morbidity and mortality. Biomarkers can detect early stages of cardiac injury so timely intervention can be provided. The B-type natriuretic peptides (Brain Natriuretic peptide [BNP] and N-terminal pro-B-type natriuretic peptide [NT-proBNP]) and troponins have been shown to predict mortality in dialysis patients. Suppression of tumorigenicity 2 (ST2) and galectin-3 are new emerging biomarkers in the field of heart failure in both the general and dialysis populations. This article aims to discuss the current evidence regarding cardiac biomarker use to diagnose myocardial injury and monitor the risk of major adverse cardiovascular events in patients undergoing dialysis.
心血管疾病是主要死因,在接受血液透析或腹膜透析的患者中,约占全因死亡率的40%。心血管风险分层是管理透析患者的一个重要方面,因为它能够早期识别高危患者,从而优化治疗干预措施以降低心血管发病率和死亡率。生物标志物可以检测心脏损伤的早期阶段,从而能够提供及时的干预。B型利钠肽(脑利钠肽[BNP]和N末端前B型利钠肽原[NT-proBNP])以及肌钙蛋白已被证明可预测透析患者的死亡率。抑瘤素2(ST2)和半乳糖凝集素-3是普通人群和透析人群中心力衰竭领域新出现的生物标志物。本文旨在讨论目前有关心脏生物标志物用于诊断透析患者心肌损伤和监测主要不良心血管事件风险的证据。