ST2 and NT-proBNP are preferred biomarkers in clinical practice for the diagnosis, risk stratification and guided therapy of STEMI and Heart Failure (HF). Purpose of the study was to determine the dynamics of NT-proBNP and ST2 and their correlations with the development of cardiovascular (CV) complications in patients with STEMI.
Methods: In total 60 patients (50 males and 10 females, mean age 60.95±9.26 years) with STEMI were examined. Patients were divided into 2 groups: group I – 22 patients with STEMI complicated with acute HF with Killip class III-IV and rhythm disturbances; group II – 38 patients with STEMI with HF Killip I. NT-proBNP and ST2 concentration in the serum were determined twice, on admission and on the 10th day of treatment.
Results: At admission mean levels of NT-proBNP were higher in group I patients with CV complications (612.8 [489.5; 860.4] pg/ml – group I) when compared to group II patients without severe CV complications (598.6 [326.6; 913.1] pg/ml – group II, p > 0.05). On the 10th day of treatment serum levels of NT-proBNP decreased to 340 [188; 434.5] pg/ml (group I) and 190.1 [113.3; 355.3] pg/ml (group II), respectively (p > 0.05). Mean levels ofST2 at admission were higher in patients with severe CV complications (61.1 [44.8; 133.6] ng/ml – group I) when compared to group II patients (40.8 [33.1; 64.3] ng/ml – group II, p < 0.05). On the 10th day of treatment mean level of ST2 decreased to 23.7 [18.8; 28.3] ng/ml (group I) and 24 [19.7; 28.7] ng/ml (group II), respectively (p > 0.05). Significant direct correlations of moderate strength were found between ST2 and NT-proBNP levels in group I on day 1 and on the 10th day of treatment (r = 0.32; p < 0.05 and r = 0.36; p < 0.05, respectively). Significant direct correlations of moderate and high strength were found between ST2 and NT-proBNP levels in group II on day 1 and on the 10th day of treatment (r = 0.367; p < 0.05 and r = 0.768; p < 0.001, respectively). Increase of ST2 and NT-proBNP above its threshold values indicates a significant risk of CV complications (sensitivity – 95.5 %, specificity – 63.2 %, AUC – 0.849, p<0.05).
In conclusion, the concentration levels of ST2 and NT-proBNP at baseline allows to predict more severe course of STEMI and the risk of CV complications. Treatment with optimal medical therapy alows to decrease biomarkers of myocardial fibrosis sST2 lower than 35 ng/ml therefore downturn the posibility of adverse outcome development in STEMI patients.