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Published on: January 28, 2020
Hepatocyte growth factor--a new marker for prognosis in acute coronary syndrome
Anna Konopka1, Jadwiga Janas, Walerian Piotrowski
1Institute of Cardiology CCU, ul. Alpejska 42, Warsaw, Poland. akonopka@ptkardio.pl
Insights
Hepatocyte growth factor (HGF) shows promise as an early marker for myocardial necrosis in acute coronary syndrome (ACS). Higher HGF levels correlate with adverse outcomes, indicating its prognostic value.
Area of Science:
- Cardiology
- Biomarker Discovery
- Molecular Medicine
Background:
- Acute coronary syndrome (ACS) necessitates reliable markers for myocardial necrosis.
- Early identification of myocardial damage is crucial for timely intervention and improved patient outcomes.
Purpose of the Study:
- To evaluate hepatocyte growth factor (HGF) as a novel biomarker for myocardial necrosis.
- To assess the prognostic significance of HGF in patients with ACS.
Main Methods:
- Plasma human HGF (hHGF) concentrations were measured in 104 ACS patients upon admission and 24 hours later.
- Correlation analysis was performed between hHGF levels and established cardiac biomarkers (NT-proBNP, troponin I).
- A three-month follow-up assessed a composite primary endpoint.
Main Results:
- Maximal hHGF levels were observed at hospital admission, decreasing significantly by 24 hours (p < 0.0001).
- Elevated hHGF levels were noted in ST-segment elevation myocardial infarction (STEMI) compared to non-STEMI.
- Patients reaching the composite endpoint had significantly higher hHGF levels (4211 pg/ml) than event-free patients (1013 pg/ml, p < 0.01).
Conclusions:
- HGF serves as a very early and effective marker of myocardial necrosis.
- HGF demonstrates sensitivity as both a short- and long-term prognostic factor in ACS patients.
Unlabelled:
This study was designed to check the properties of hepatocyte growth factor (HGF) as a new marker of myocardial necrosis.
Materials And Method:
In one hundred and four patients with acute coronary syndrome (ACS), plasma human HGF (hHGF) concentrations were assessed twice, i.e. just after admission to hospital and 24 h afterwards. The primary composite endpoint was assessed at three-month follow-up.
Results:
The maximal concentration of hHGF (1902 pg/ml) was reached at the time of admission to hospital due to ACS with significant decrease 24 h after the first measurement (705 pg/ml p < 0.0001). hHGF levels in ST segment elevation myocardial infarction (STEMI) were higher than in non-ST segment elevation myocardial infarction (NSTEMI) and in patients who reached composite primary endpoint (33 patients-4211 pg/ml) vs. event-free 71 patients (1013 pg/ml p < 0.01). The correlation between values of hHGF and N-terminal prohormone B-type natriuretic peptide and cardiac troponin I was revealed.
Conclusion:
HGF is a very early, good marker of myocardial necrosis and a sensitive short- and long-term prognostic factor in ACS.
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