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Published on: January 28, 2020
Prognostic value of growth differentiation factor-15 3 months after an acute chest pain admission
Gard Mikael Sæle Myrmel1, Ole-Thomas Steiro1, Hilde Lunde Tjora2
1Department of Heart Disease, Haukeland University Hospital, Bergen, Norway.
Insights
Measuring Growth Differentiation Factor-15 (GDF-15) three months after non-ST-elevation acute coronary syndrome (NSTE-ACS) predicts long-term mortality and cardiovascular events. Changes in GDF-15 levels also offer valuable prognostic insights.
Area of Science:
- Cardiology
- Biomarkers
- Prognostics
Background:
- Growth differentiation factor-15 (GDF-15) is a known predictor of adverse outcomes in acute chest pain patients.
- Its prognostic utility in the subacute phase of non-ST-elevation acute coronary syndrome (NSTE-ACS) requires further investigation.
Purpose of the Study:
- To evaluate the prognostic value of GDF-15 levels measured 3 months post-NSTE-ACS admission.
- To determine if GDF-15 predicts long-term all-cause mortality and major adverse cardiovascular events.
Main Methods:
- GDF-15 levels were measured at baseline and 3 months in 758 patients with suspected NSTE-ACS.
- Patients were followed for a median of 1540 days for all-cause mortality and a composite endpoint (mortality, myocardial infarction, heart failure hospitalization).
Main Results:
- Patients with GDF-15 ≥1200 pg/mL at 3 months had significantly higher rates of death (18%) and composite events (25%) compared to those with GDF-15 <1200 pg/mL (1.7% and 4%, respectively).
- Elevated 3-month GDF-15 levels were independently associated with increased risk of all-cause mortality and the composite endpoint.
- A 10% increase in GDF-15 from baseline to 3 months predicted higher all-cause mortality risk.
Conclusions:
- High GDF-15 concentrations 3 months after NSTE-ACS admission are strong independent predictors of long-term mortality and cardiovascular events.
- GDF-15 offers prognostic information beyond traditional risk factors and troponin T.
- Changes in GDF-15 levels provide additional prognostic value.
Objective:
Growth differentiation factor-15 (GDF-15) is a predictor of death and cardiovascular events when measured during index hospitalisation in patients with acute chest pain. This study investigated the prognostic utility of measuring GDF-15 3 months after an admission with suspected non-ST-elevation acute coronary syndrome (NSTE-ACS).
Methods:
GDF-15 was measured at baseline and 3 months after admission in 758 patients admitted with suspected NSTE-ACS. Patients were followed for a median of 1540 (IQR: 1087-1776) days after the 3-month visit. The primary endpoint was all-cause mortality, while the secondary composite endpoint included all-cause mortality, incident myocardial infarction and heart failure hospitalisation during follow-up.
Results:
In patients with GDF-15 ≥1200 pg/mL (n=248), 18% died and 25% met the composite endpoint. In patients with GDF-15 <1200 pg/mL (n=510), 1.7% died and 4% met the composite endpoint. The GDF-15 concentration (log2 transformed) at 3 months was significantly associated with all-cause mortality (adjusted HR: 2.2, 95% CI: 1.4 to 3.3, p<0.001) and the composite endpoint (adjusted HR: 1.9, 95% CI: 1.4 to 2.7, p<0.001), independently of traditional risk factors and baseline troponin T. A 10% change in GDF-15 concentration from baseline to the 3-month visit was associated with increased risk of all-cause mortality (HR: 1.06, 95% CI: 1.01 to 1.13, p=0.031), adjusting for baseline GDF-15 concentrations.
Conclusions:
High GDF-15 concentrations 3 months after admission for suspected NSTE-ACS are associated with long-term mortality and cardiovascular events, independent of traditional risk factors and troponin T. A change in GDF-15 concentration can provide prognostic information.
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