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Published on: January 28, 2020
Plasma urocortin in acute myocardial infarction patients
Arintaya Phrommintikul1, Sivaporn Sivasinprasasn, Narissara Lailerd
1Cardiac Electrophysiology Research and Training Center, Cardiology Division, Department of Internal Medicine, Chiang Mai University, Chiang Mai, Thailand.
Insights
Plasma urocortin levels are elevated in acute myocardial infarction (AMI) patients for five days. High early plasma urocortin predicts increased mortality, and combining it with NT-proBNP improves prognostic accuracy.
Area of Science:
- Cardiology
- Biomarkers
- Clinical Research
Background:
- The cardioprotective role of urocortin is proposed but its function in acute myocardial infarction (AMI) is unclear.
- Investigating plasma urocortin levels and their prognostic value in AMI patients is crucial.
Purpose of the Study:
- To determine the plasma profile of urocortin in AMI patients.
- To evaluate the long-term prognostic performance of plasma urocortin in AMI.
Main Methods:
- Sixty-six AMI patients and 21 healthy controls were enrolled.
- Plasma urocortin levels were measured on days 0, 1, 3, 5, and at 3 and 6 months post-onset.
- Primary endpoint was 1-year mortality; secondary endpoint was a composite of death and adverse cardiac events.
Main Results:
- Plasma urocortin was elevated in AMI patients for up to 5 days.
- Day 0 urocortin showed an AUC of 0.750 for mortality prediction (P=0.004).
- Combining urocortin and NT-proBNP demonstrated superior prognostic performance for mortality and adverse events.
Conclusions:
- Elevated plasma urocortin is observed in AMI patients for 5 days post-onset.
- High plasma urocortin within 24 hours of onset is linked to increased mortality.
- Combined urocortin and NT-proBNP levels enhance prognostic accuracy in AMI.
Background:
Despite its proposed cardioprotective effect, the role of plasma urocortin in acute myocardial infarction (AMI) remains unknown. We investigated plasma profile of urocortin in AMI patients and evaluated its long-term prognostic performance.
Material And Methods:
Sixty-six AMI patients and 21 healthy subjects were included in this study. Blood samples for urocortin were collected on days 0 (onset), 1, 3 and 5 and at 3 and 6 months. Primary endpoint was mortality within 1 year of follow-up. Secondary endpoint was combined death and nonfatal adverse cardiac events (i.e. myocardial reinfarction, urgent revascularization or hospitalization due to heart failure) within 1 year.
Results:
During follow-up at 1 year, 38 (57·6%) patients were alive without cardiac events, nine (13·6%) had nonfatal cardiac events and 17 (25·8%) died. Plasma urocortin in AMI patients were increased on days 0, 1, 3 and 5 (P<0·05 vs. control). The receiver-operating characteristic curve showed an area under curve (AUC) of day 0 urocortin to be 0·750 with 95% confidence interval (CI) of 0·619-0·881 (P=0·004), whereas AUC of NT-proBNP was 0·857 (95% CI, 0·722-0·992; P=0·003). Sensitivity values for predicting the mortality of urocortin NT-proBNP and a combined urocortin and NT-proBNP were 0·81 (95% CI, 0·54-0·95), 0·86 (95% CI, 0·42-0·99) and 1·0 (95% CI, 0·56-1·0), respectively.
Conclusions:
Plasma urocortin level is elevated in AMI patients for 5 days from onset. High plasma urocortin within 24 h after the onset is associated with increased mortality. Combined urocortin and NT-proBNP enhance prognostic performance in AMI patients.
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