Institute of Nephrology and Blood Purification, The First Affiliated Hospital of Jinan University, Jinan University, Guangzhou, China.
Fifth Department of Medicine (Nephrology/Endocrinology/Rheumatology), University Medical Centre Mannheim, University of Heidelberg, Heidelberg, Germany.
Bioengineered. 2021 Dec;12(2):12407-12419. doi: 10.1080/21655979.2021.2005219.
This study aims to explore the effect of N-terminal pro-brain natriuretic peptide (NT-proBNP) variability (mean absolute difference of the log2 NT-proBNP level measured in hospital) on the prognosis of patients with cardiorenal syndrome (CRS) type 2. Patients with CRS type 2 were retrospectively included. The varied NT-proBNP indications were analyzed. They were NT-proBNP I(pre-treatment), NT-proBNP II(post-treatment), NT-proBNP II/I, ΔNT-proBNP, log2 (NT-proBNP) variability and mean log2 (NT-proBNP). A logistic regression model and survival curves (Kaplan-Meier analysis) were built to identify independent predictors associated with poor prognosis. The primary outcomes were major adverse renal and cardiac events. The secondary outcome was all-cause mortality. From 2012 to 2016, 136 patients were included in this study with 69 (50.7%) had high log2 (NT-proBNP) variability level. The optimal cutoff level for each NT-proBNP indication that predicts poor prognosis was calculated, and the area under curves ranged from 0.668 to 0.891 with different indications. Kaplan-Meier analysis revealed that there was significantly correlated with prevalence of primary outcomes and NT-proBNP variability. The hazard ratios (HRs) ranged from 1.67 to 6.61 with different indications. The multivariate regression analyses also identified the risk of the primary outcomes were associated with elevated NT-proBNP values, except NT-proBNP I. The odds ratio (ORs) ranged from 1.83 to 6.61 with different indications. When analyzing the relationship between NT-proBNP variability and all-cause mortality, the results were the same. NT-proBNP variability might serve as an independent predictor for poor prognosis and all-cause mortality in patients with CRS type 2.
本研究旨在探讨 N 末端脑利钠肽前体(NT-proBNP)变异性(住院期间测量的 log2 NT-proBNP 水平的平均绝对差值)对 2 型心肾综合征(CRS)患者预后的影响。回顾性纳入 2 型 CRS 患者。分析了变化的 NT-proBNP 指标。它们是 NT-proBNP I(预处理)、NT-proBNP II(后处理)、NT-proBNP II/I、ΔNT-proBNP、log2(NT-proBNP)变异性和平均 log2(NT-proBNP)。建立了逻辑回归模型和生存曲线(Kaplan-Meier 分析),以确定与不良预后相关的独立预测因素。主要结局是主要不良肾脏和心脏事件。次要结局是全因死亡率。2012 年至 2016 年,共纳入 136 例患者,其中 69 例(50.7%)log2(NT-proBNP)变异性水平较高。计算了每个预测不良预后的 NT-proBNP 指标的最佳截断值,不同指标的曲线下面积范围为 0.668 至 0.891。Kaplan-Meier 分析显示,与主要结局和 NT-proBNP 变异性的发生率显著相关。不同指标的风险比(HRs)范围为 1.67 至 6.61。多变量回归分析也表明,主要结局的风险与升高的 NT-proBNP 值相关,除了 NT-proBNP I。不同指标的比值比(ORs)范围为 1.83 至 6.61。在分析 NT-proBNP 变异性与全因死亡率之间的关系时,结果相同。NT-proBNP 变异性可能是 2 型 CRS 患者不良预后和全因死亡率的独立预测因素。