Pintado María-Consuelo, Maceda Lara, Trascasa María, Arribas Ignacio, De Pablo Raúl
Critical Care Unit, Hospital Universitario Príncipe de Asturias, Carretera Alcalá-Meco SN, 28805, Alcalá de Henares, Madrid, Spain.
University of Alcalá, Alcalá de Henares, Madrid, Spain.
Egypt Heart J. 2022 Apr 28;74(1):35. doi: 10.1186/s43044-022-00275-9.
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.
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).
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.
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。尽管已经研究了几种生物标志物用于风险分层和预后评估,但基于其预后价值,尚无一种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相关。本研究的目的是评估在急性心肌梗死患者中,测定copeptin和肝细胞生长因子对医院死亡率风险和1年随访死亡率的早期预后价值。在我们的回顾性观察研究中,我们测定了急性心肌梗死患者入院时采集的血样中的肝细胞生长因子和copeptin;并对他们进行随访直至1年。
84例患者纳入研究,主要为男性(65%),中位年龄为70.3±13.56岁。医院死亡率为11.9%。入院时死亡的患者血浆copeptin水平在统计学上显著更高(145.60 pmol/L [52.21 - 588.50] 对比 24.79 pmol/L [10.90 - 84.82],p < 0.01)。然而,我们发现肝细胞生长因子血浆水平与医院死亡率之间无统计学显著关联(381.05 pg/ml [189.95 - 736.65] 对比 355.24 pg/ml [175.55 - 521.76],p = 0.73)。1年随访死亡率为21.4%。次年死亡的患者入院时血浆copeptin水平更高(112.28 pmol/L [25.10 - 418.27] 对比 23.82 pmol/L [10.96 - 77.30],p < 0.02)。对于肝细胞生长因子,我们也未发现肝细胞生长因子血浆水平与1年随访死亡率之间存在关联(350.00 pg/ml [175.05 - 555.08] 对比 345.53 pg/ml [183.68 - 561.15],p = 0.68)。
在急性心肌梗死患者中,入院时测定copeptin可能是评估这些患者预后的有用工具,因为其升高与更高的医院死亡率和更高的1年随访死亡率相关。在测定肝细胞生长因子的情况下,我们未发现这种关联。