急性心肌梗死患者入院时的预后工具: copeptin 和肝细胞生长因子。

María-Consuelo Pintado, Lara Maceda, María Trascasa, Ignacio Arribas, Raúl De Pablo
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引用次数: 0

摘要

背景:急性冠状动脉综合征的及时评估和治疗已被证明可降低死亡率。尽管已研究了多种用于风险分层和预后的生物标志物,但没有一种生物标志物被推荐用于指导治疗。Copeptin 和肝细胞生长因子与急性心肌梗死患者的不良预后有关。本研究的目的是评估急性心肌梗死患者的 copeptin 和肝细胞生长因子测量值对住院死亡率风险和随访 1 年死亡率的早期预后价值。在这项回顾性观察研究中,我们对急性心肌梗死患者入院时采集的血液样本中的肝细胞生长因子和肝素进行了测定,并对其进行了为期一年的随访:研究共纳入 84 名急性心肌梗死患者,主要为男性(65%),中位年龄为 70.3 ± 13.56 岁。住院死亡率为 11.9%。入院时死亡的患者血浆中的 copeptin 水平显著高于入院时死亡的患者(145.60 pmol/L [52.21-588.50] vs. 24.79 pmol/L [10.90-84.82],P 0.01)。然而,我们发现血浆中的肝细胞生长因子水平与住院死亡率(381.05 pg/ml [189.95-736.65] vs. 355.24 pg/ml [175.55-521.76],P 0.73)之间没有统计学意义。随访 1 年的死亡率为 21.4%。次年死亡的患者入院时血浆中的 copeptin 水平更高(112.28 pmol/L [25.10-418.27] vs. 23.82 pmol/L [10.96-77.30],P 0.02)。在肝细胞生长因子方面,我们也发现肝细胞生长因子血浆水平与1年随访死亡率之间没有关联(350.00 pg/ml [175.05-555.08] vs. 345.53 pg/ml [183.68-561.15],P 0.68):在急性心肌梗死患者中,入院时测量 copeptin 可作为评估这些患者预后的有用工具,因为 copeptin 升高与较高的住院死亡率和 1 年随访死亡率相关。在肝细胞生长因子的测量中,我们没有发现这种关联。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prognostic tools at hospital arrival in acute myocardial infarction: copeptin and hepatocyte growth factor.

Background: Prompt evaluation and treatment of acute coronary syndrome has demonstrated to reduce mortality. Although several biomarkers have been studied for risk stratification and prognostic purposes, none is recommended to guide treatment based on its prognostic value. Copeptin and hepatocyte growth factor have been associated with poor outcome in patients with acute myocardial infarction. The aim of this study is to evaluate the early prognostic value of measurements of copeptin and hepatocyte growth factor for hospital mortality risk and 1-year-follow-up mortality, in patients with acute myocardial infarction. In our retrospective observational study, we measured hepatocyte growth factor and copeptin in blood samples collected at hospital arrival in patients with acute myocardial infarction; and follow-up them until 1-year.

Results: 84 patients with were included in the study, mainly male (65%) with a median age of 70.3 ± 13.56 years. Hospital mortality was 11.9%. Plasma levels of copeptin at hospital arrival were statistically significant higher in patients who died during hospital admission (145.60 pmol/L [52.21-588.50] vs. 24.79 pmol/L [10.90-84.82], p 0.01). However, we found no statistically significant association between plasma levels of hepatocyte growth factor and hospital mortality (381.05 pg/ml [189.95-736.65] vs. 355.24 pg/ml [175.55-521.76], p 0.73). 1-year follow-up mortality was 21.4%. Plasma levels of copeptin at hospital arrival were higher in those patients who died in the following year (112.28 pmol/L [25.10-418.27] vs. 23.82 pmol/L [10.96-77.30], p 0.02). In the case of HGF, we also find no association between hepatocyte growth factor plasma levels and 1 -year follow-up mortality (350.00 pg/ml [175.05-555.08] vs. 345.53 pg/ml [183.68-561.15], p 0.68).

Conclusions: In patients with acute myocardial infarction measurement of copeptin at hospital arrival could be a useful tool to assess the prognosis of these patients, since their elevation is associated with a higher hospital mortality and higher 1-year follow-up mortality. We have not found this association in the case of hepatocyte growth factor measurement.

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