Department of Cardiovascular Research, Istituto di Ricerche Farmacologiche Mario Negri, via La Masa 19, Milan, Italy.
Eur J Heart Fail. 2010 Apr;12(4):338-47. doi: 10.1093/eurjhf/hfp206. Epub 2010 Jan 22.
Though various neurohormonal systems are concurrently activated during heart failure (HF), their biological effectors are not always easy to measure due to their short life in vivo, instability in biological samples, or very low concentrations. We measured the plasma concentrations of four stable precursor fragments of neurohormonal systems in patients with chronic HF and evaluated their relationship with outcome.
This study was performed in 1237 patients with chronic and stable HF enrolled in the GISSI-heart failure trial (GISSI-HF). The following four precursor fragments, mid-regional pro-atrial natriuretic peptide (MR-proANP), mid-regional pro-adrenomedullin (MR-proADM), C-terminal pro-endothelin-1 (CT-proET-1) and C-terminal pro-vasopressin (CT-proAVP or copeptin), were measured at randomization and after 3 months. Baseline concentrations were independent predictors of clinical outcome (median follow-up 3.9 years). The addition of MR-proANP improved net reclassification for mortality when added to multivariable models based on clinical risk factors alone [net reclassification improvement (NRI) = 0.12, P = 0.0007] or together with NT-proBNP (NRI = 0.06, P = 0.01). Changes in MR-proANP concentrations were related to mortality [HR (95% CI) 1.38 (0.99-1.93), P = 0.0614 and 1.58 (1.13-2.21), P = 0.0078 in the middle and highest vs. lowest tertiles], while changes in the other markers were not.
In patients with chronic and stable HF enrolled in a multicentre, randomized, clinical trial, measurement of stable precursor fragments of vasoactive peptides provided prognostic information independent of natriuretic peptides which are currently the best biomarkers for risk stratification.
尽管在心力衰竭(HF)期间会同时激活各种神经激素系统,但由于它们在体内的寿命短、生物样本不稳定或浓度非常低,其生物效应物并不总是容易测量。我们测量了慢性 HF 患者的四种神经激素系统稳定前体片段的血浆浓度,并评估了它们与结局的关系。
这项研究在 GISSI-心力衰竭试验(GISSI-HF)中招募的 1237 例慢性和稳定 HF 患者中进行。在随机分组时和 3 个月后测量了以下四种前体片段:中段前利尿钠肽(MR-proANP)、中段肾上腺髓质素(MR-proADM)、C 端内皮素-1(CT-proET-1)和 C 端加压素(CT-proAVP 或 copeptin)。基线浓度是临床结局的独立预测因子(中位随访 3.9 年)。MR-proANP 的加入改善了仅基于临床危险因素的多变量模型的死亡率的净重新分类[净重新分类改善(NRI)=0.12,P=0.0007]或与 NT-proBNP 一起加入时的死亡率(NRI=0.06,P=0.01)。MR-proANP 浓度的变化与死亡率相关[HR(95%CI)1.38(0.99-1.93),P=0.0614 和 1.58(1.13-2.21),P=0.0078 在中间和最高与最低三分位数之间],而其他标志物的变化则没有。
在参加多中心、随机、临床试验的慢性和稳定 HF 患者中,测量血管活性肽的稳定前体片段提供了独立于目前用于风险分层的最佳生物标志物利钠肽的预后信息。