» Articles » PMID: 39819309

Short-term Predictive Value of SST2 in Patients with STEMI Following Primary PCI: a Prospective Observational Study

Overview
Publisher Biomed Central
Date 2025 Jan 17
PMID 39819309
Authors
Affiliations
Soon will be listed here.
Abstract

Aim: The objective of this study was to investigate the level of soluble suppression of tumorigenicity-2 (sST2) in patients with acute ST-segment elevation myocardial infarction (STEMI) following primary percutaneous coronary intervention (PCI), and to provide a new biomarker for clinical management and prognosis assessment.

Method: This was a prospective study. 148 STEMI patients following primary PCI were enrolled and divided into 2 groups by the median value of sST2 and afterwards followed up for 30 days to access the occurrence of major adverse cardiac events (MACEs), which were defined as cardiovascular death, heart failure and recurrent MI.

Results: sST2 ranged from 20.57 to 98.96 ng/mL. High sST2 group had higher MACEs rate compared to low sST2 group (28.8% vs. 8.0%, P = 0.001). sST2 was positively correlated with age (r = 0.181, P = 0.027), SYNTAX score (r = 0.257, P = 0.002), high-sensitive C-reactive protein (hs-CRP) (r = 0.225, P = 0.006), B-type natriuretic peptide (BNP) (r = 0.225, P = 0.006) and negatively with left ventricle ejection fraction (LVEF) (r = -0.197, P = 0.016). After adjustment for clinical variables, sST2 level (OR 3.680, P = 0.015) and LVEF (OR 0.880, P < 0.001) remained independent predictors of 30-days MACEs. In receiver operating characteristic curve (ROC) analyses, the area under the curve (AUC) of sST2 for predicting 30-days MACEs was 0.755(P < 0.001). The AUC of sST2 combining hs-CRP and LVEF for prediction was 0.828(95%CI [0.743-0.912], P < 0.001).

Conclusion: sST2 level after primary PCI was an independent risk factor of MACEs in STEMI patients through 30 days follow-up.

References
1.
Chen W, Lin A, Yu Y, Zhang L, Yang G, Hu H . Serum Soluble ST2 as a Novel Inflammatory Marker in Acute Ischemic Stroke. Clin Lab. 2018; 64(9):1349-1356. DOI: 10.7754/Clin.Lab.2018.180105. View

2.
Gruzdeva O, Dyleva Y, Uchasova E, Akbasheva O, Karetnikova V, Kashtalap V . Biological markers and cardiac remodelling following the myocardial infarction. Aging (Albany NY). 2019; 11(11):3523-3535. PMC: 6594818. DOI: 10.18632/aging.101994. View

3.
Willems S, Sels J, Flier S, Versteeg D, Buhre W, de Kleijn D . Temporal changes of soluble ST2 after cardiovascular interventions. Eur J Clin Invest. 2012; 43(2):113-20. DOI: 10.1111/eci.12022. View

4.
Zhang Q, Hu M, Ma S . Association of Soluble Suppression of Tumorigenicity with No-Reflow Phenomenon and Long-Term Prognosis in Patients with Non-ST-Segment Elevation Acute Coronary Syndrome after Percutaneous Coronary Intervention. J Atheroscler Thromb. 2021; 28(12):1289-1297. PMC: 8629709. DOI: 10.5551/jat.59832. View

5.
Sanada S, Hakuno D, Higgins L, Schreiter E, McKenzie A, Lee R . IL-33 and ST2 comprise a critical biomechanically induced and cardioprotective signaling system. J Clin Invest. 2007; 117(6):1538-49. PMC: 1865027. DOI: 10.1172/JCI30634. View