Key result
In STEMI patients treated with primary PCI, GDF-15 concentration at 12 hours was a strong predictor of 30-day mortality (HR 2.99; 95% CI 2.18-4.09).
Why the study?
While GDF-15 in STEMI has shown prognostic value using first-generation radioimmunoassays, its temporal dynamics and predictive value using a fully automated electrochemiluminescence assay needed evaluation.
Does GDF-15 concentration predict mortality and cardiovascular hospitalization in STEMI patients treated with primary PCI?
Cohort (n=1,026)
Does GDF-15 concentration predict mortality and cardiovascular hospitalization in STEMI patients treated with primary PCI?
Hazard Ratio: 2.99 (95% CI 2.18–4.09)
GDF-15 levels peak at 12 hours in STEMI patients and are strong predictors of both 30-day and 3-year mortality, improving clinical risk stratification.
May aid early risk stratification post-PCI; leaves open incremental value over standard models.
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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Rueda et al. (2019) conducted a cohort in ST-elevation myocardial infarction (STEMI) (n=1,026). Growth differentiation factor 15 (GDF-15) concentration was evaluated on 30-day mortality (HR 2.99, 95% CI 2.18-4.09). In STEMI patients treated with primary PCI, GDF-15 concentration at 12 hours was a strong predictor of 30-day mortality (HR 2.99; 95% CI 2.18-4.09).
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