Evaluation of Serum Soluble Suppression of Tumorigenicity 2 (sST-2) in Ischemic Heart Disease | ||||
| Benha Medical Journal | ||||
| Articles in Press, Accepted Manuscript, Available Online from 11 May 2025 PDF (619.09 K) | ||||
| Document Type: Original Article | ||||
| DOI: 10.21608/bmfj.2025.344138.2285 | ||||
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| Authors | ||||
Mona Eltoukhy Fouda1; Nancy Ibraheem  2; Hesham Khalid Rashid3; Iman Ramadan Abdel Gwad4; Amira Osama Abd El-Ghafar4
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| 1Clinical and Chemical Pathology department, Faculty of Medicine, Benha University, Egypt | ||||
| 2Faculty of Medicine, Benha University, Benha, Egypt. | ||||
| 3Cardiology Department, Faculty of Medicine, Benha University, Benha, Egypt. | ||||
| 4Clinical and Chemical Pathology Department, Faculty of Medicine, Benha University, Benha, Egypt. | ||||
| Abstract | ||||
| Background: Ischemic heart disease (IHD) remains a primary cause of morbidity and mortality worldwide. Identifying effective biomarkers for early diagnosis is crucial for optimal patient outcomes. Serum Soluble Suppression of Tumorigenicity 2 (sST-2), a member of the interleukin-1 receptor family, has gained attention as a novel marker for myocardial stress and injury. Methods: This comparative cross-sectional study, conducted at Benha University Hospitals between February and December 2023, involved 60 IHD patients (30 with acute myocardial infarction [AMI] and 30 with angina pectoris) and 20 healthy controls. Serum sST-2 levels and traditional cardiac biomarkers (troponin I, CK, and CK-MB) were measured using ELISA. Statistical analyses were performed to assess correlations between sST-2 and various clinical parameters, including BMI, lipid profiles, blood pressure, and LVEF. Results: sST-2 levels were significantly elevated in AMI (78.3 ± 37.3 ng/L) and angina patients (71.4 ± 39.7 ng/L) compared to controls (26.1 ± 6.9 ng/L, P < 0.001). Troponin I and CK-MB were also higher in both patient groups versus controls (P < 0.001). Positive correlations were identified between sST-2 and BMI (r = 0.314, P = 0.005), SBP (r = 0.303, P = 0.006), and troponin I (r = 0.396, P < 0.001), while significant negative correlations were noted with LVEF (r = -0.526, P < 0.001). Conclusion: Serum sST-2 shows promise as a diagnostic and prognostic biomarker for IHD. Integrating sST-2 into clinical practice could improve the early identification and management of IHD, particularly in acute coronary syndromes. | ||||
| Keywords | ||||
| Ischemic heart disease; sST-2; myocardial infarction; biomarkers; angina pectoris | ||||
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