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Updated: Jan 30, 2026

Acute Myocardial Infarction in Rats
Published on: February 16, 2011
Acute-phase dynamics and prognostic value of growth differentiation factor-15 in ST-elevation myocardial infarction
Ferran Rueda1,2, Josep Lupón1,2, Cosme García-García2,3
1Department of Cardiology, Heart Institute, Germans Trias i Pujol University Hospital, Badalona (Barcelona), Spain.
Insights
Growth Differentiation Factor 15 (GDF-15) levels peak 12 hours after ST-elevation myocardial infarction (STEMI) and predict both short- and long-term patient outcomes. This biomarker aids in risk stratification for STEMI patients.
Area of Science:
- Cardiology
- Biomarkers
- Clinical Diagnostics
Background:
- Growth Differentiation Factor 15 (GDF-15) is a prognostic biomarker in ST-elevation myocardial infarction (STEMI).
- Previous studies utilized first-generation radioimmunoassays for GDF-15 assessment.
- Automated electrochemiluminescence assays offer a more efficient method for GDF-15 measurement.
Purpose of the Study:
- To investigate the temporal dynamics of GDF-15 in STEMI patients.
- To evaluate the predictive value of GDF-15 levels for short-term (30-day) and long-term (3-year) outcomes.
- To assess GDF-15's utility in improving risk stratification models for STEMI.
Main Methods:
- Prospective study of 1026 STEMI patients treated with primary percutaneous coronary intervention.
- Measurement of circulating GDF-15 concentrations at admission (0 h), 12 h, and 24 h using an automated electrochemiluminescence assay.
- Analysis of GDF-15 dynamics and its association with 30-day and 3-year mortality and cardiovascular hospitalizations.
Main Results:
- GDF-15 concentrations peaked at 12 hours (1731 pg/mL) and remained elevated at 24 hours (1510 pg/mL) post-STEMI admission.
- GDF-15 was a strong predictor of 30-day mortality, with hazard ratios increasing at 12 hours.
- Elevated GDF-15 levels at all time points (0, 12, 24 h) predicted 3-year mortality and a composite of mortality and cardiovascular hospitalization.
Conclusions:
- GDF-15 exhibits dynamic changes in STEMI, peaking at 12 hours and remaining elevated.
- GDF-15 measurement within the first 24 hours is valuable for predicting short- and long-term outcomes in STEMI.
- GDF-15 can serve as a useful addition to existing risk stratification tools for STEMI patients.
Abstract:
Background Growth differentiation factor 15 (GDF-15) in ST-elevation myocardial infarction (STEMI) is prognostic in first-generation radioimmunoassays. We examined GDF-15 temporal dynamics in STEMI and its predictive value using a first fully automated GDF-15 electrochemiluminescence assay. Methods In this prospective study, circulating GDF-15 concentration was measured at admission (0 h), 12 h and 24 h in 1026 consecutive STEMI patients treated between February 2011 and May 2016 with primary percutaneous coronary intervention. GDF-15 dynamics (0 h, 12 h, 24 h) and predictive value (30 days and 3 years) were examined. Results Median GDF-15 concentration was 1443 pg/mL at 0 h, 1731 pg/mL at 12 h and 1510 pg/mL at 24 h (p<0.001). During follow-up, 94 patients died (9.2%) and 154 (15.0%) were hospitalized. GDF-15 was a strong predictor of 30-day mortality (hazard ratio [HR] 1.76, 95% confidence interval [CI], 1.33-2.34 at 0 h; HR 2.99 [95% CI, 2.18-4.09] at 12 h, and HR 1.97 [95% CI, 1.47-2.63] at 24 h) in multivariable Cox proportional hazards models. GDF-15 improved discrimination and reclassification of a clinical risk model. GDF-15 was also associated with 3-year mortality (HR 1.31 [95% CI, 1.04-1.65] at 0 h, HR 1.42 [95% CI, 1.10-1.84] at 12 h, and HR 1.51 [95% CI, 1.16-1.96] at 24 h) and 3-year composite of mortality and cardiovascular hospitalization (HR 1.17 [95% CI, 1.01-1.37] at 0 h, HR 1.20 [95% CI, 1.02-1.42] at 12 h, and HR 1.27 [95% CI, 1.08-1.50] at 24 h). Conclusions GDF-15 peaked at 12 h and remained elevated at 24 h in STEMI. GDF-15 measurement during the first 24 h in STEMI is valuable for predicting especially short- but also long-term outcomes, and may be a useful addition to risk stratification.
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