Department of Cardiology, University of Heidelberg, Im Neuenheimer Feld 410, 69120, Heidelberg, Germany.
Clin Res Cardiol. 2011 Dec;100(12):1059-67. doi: 10.1007/s00392-011-0340-1. Epub 2011 Jul 16.
The role of serial NT-proBNP measurements in patients suffering from chronic systolic heart failure (CHF) who already receive individually optimized pharmacotherapy is still unresolved.
NT-proBNP was assessed at baseline and at 6 months follow-up in 504 stable CHF patients treated with individually optimized pharmacotherapy. After assessment of clinical stability at 6 months, patients were followed up for at least 1 year. The combined primary endpoint was defined as death, hospitalization due to cardiac reasons or heart transplantation in 1-year follow-up. We stratified our patients according to two principles: first, a percent change of value (CV) between the first and second measurement of NT-proBNP and secondly, the transformed logarithm of NT-proBNP measured at 6 months.
During the follow-up period of 1 year, 50 patients (9.9%) reached the combined primary endpoint. Stratification according to percentage CV was less accurate in predicting endpoint-free survival compared to a classification in categories of lnNT-proBNP measured at 6 months (ROC AUC = 0.615; 95% CI 0.525-0.70 vs. ROC AUC = 0.790; 95% CI 0.721-0.856, respectively). When entered into proportional hazard regression analysis, lnNT-proBNP measured at 6 months remained an independent predictor of the combined primary endpoint with an associated HR of 2.53 (95% CI 1.385-4.280).
To date, this is the largest analysis of serial NT-proBNP measurements in patients with CHF receiving individually optimized medical therapy. These data suggest that a single NT-proBNP measurement after 6 months in stable clinical conditions may have higher predictive value than stratification of change in serial measurements.
在接受个体化优化药物治疗的慢性收缩性心力衰竭(CHF)患者中,连续测定 NT-proBNP 的作用仍未解决。
在 504 例接受个体化优化药物治疗的稳定 CHF 患者中,于基线和 6 个月随访时评估 NT-proBNP。在 6 个月时评估临床稳定性后,对患者进行了至少 1 年的随访。主要复合终点定义为 1 年随访期间死亡、因心脏原因住院或心脏移植。我们根据两个原则对患者进行分层:首先,是 NT-proBNP 第一和第二次测量值之间的变化百分比(CV),其次,是测量的 6 个月时的 NT-proBNP 转换后的对数值。
在 1 年的随访期间,有 50 例患者(9.9%)达到了主要复合终点。与分类为 6 个月时测量的 lnNT-proBNP 相比,按百分比 CV 分层在预测无终点生存方面的准确性较低(ROC AUC 分别为 0.615[95%CI 0.525-0.70]和 0.790[95%CI 0.721-0.856])。当进入比例风险回归分析时,6 个月时测量的 lnNT-proBNP 仍然是主要复合终点的独立预测因子,其相关 HR 为 2.53(95%CI 1.385-4.280)。
迄今为止,这是在接受个体化优化药物治疗的 CHF 患者中进行的最大规模的连续 NT-proBNP 测量分析。这些数据表明,在稳定的临床条件下,6 个月后单次 NT-proBNP 测量的预测价值可能高于连续测量的变化分层。