Key result
Among 1020 patients with acute heart failure (162 deaths at 1 year), sST2 and NT-proBNP were significantly associated with mortality regardless of etiology, while galectin-3 lacked added value.
Why the study?
Do soluble ST2 (sST2), galectin-3, and NT-proBNP predict 1-year all-cause death in patients with acute heart failure?
Cohort (n=1,020)
Do soluble ST2 (sST2), galectin-3, and NT-proBNP predict 1-year all-cause death in patients with acute heart failure?
sST2 and NT-proBNP provide etiology-independent prognostic value for 1-year mortality in acute heart failure, while galectin-3 lacks added prognostic utility in ischemic heart failure.
May aid acute HF risk stratification; leaves open whether these biomarkers improve outcomes in prospective trials.
AIM: To investigate the prognosis of soluble ST2 (sST2), galectin-3 and N-terminal pro-B-type natriuretic peptide (NT-proBNP) for death related to ischemic and nonischemic etiology of acute heart failure (HF). METHODS: The associations between biomarkers and death were determined in 1020 patients admitted to hospital with acute HF. RESULTS: During 1-year follow-up, 162 patients died. Multivariable regression analysis showed that the hazard ratios of sST2 and NT-proBNP for 1-year all-cause death was similar and remained significant between ischemic and nonischemic HF patients. However, galectin-3 was not significantly associated with death when sST2 and NT-proBNP were incorporated into model in ischemic HF patients. CONCLUSION: There is no etiology dependent prognostic ability of NT-proBNP or ST2 in patients with acute HF, but for galectin-3 there is no added prognostic ability in ischemic HF.
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Zhang et al. (2018) conducted a cohort in Acute heart failure (n=1,020). sST2, galectin-3, and NT-proBNP was evaluated on 1-year all-cause death. Among 1020 patients with acute heart failure (162 deaths at 1 year), sST2 and NT-proBNP were significantly associated with mortality regardless of etiology, while galectin-3 lacked added value.
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