Authors
- Fatma Nihan Turhan Caglarą — Department of Cardiology, Bakirkoy Dr. Sadi Konuk Education and Research Hospital, Istanbul, Turkey — ORCID: 0000-0001-7925-2398
- Nilgun Isiksacan — Department of Biochemistry, Bakirkoy Dr. Sadi Konuk Education and Research Hospital, Istanbul, Turkey — ORCID: 0000-0002-0230-6500
- Ismail Biyik — Department of Cardiology, Usak State Hospital, Usak, Turkey
- Ismail Ungan — Department of Cardiology, Bakirkoy Dr. Sadi Konuk Education and Research Hospital, Istanbul, Turkey
- Selcuk Opaną — Department of Cardiology, Bakirkoy Dr. Sadi Konuk Education and Research Hospital, Istanbul, Turkey — ORCID: 0000-0002-6335-5250
- Hulya Cebeą — Department of Cardiology, Bakirkoy Dr. Sadi Konuk Education and Research Hospital, Istanbul, Turkey
- Ibrahim Faruk Akturką — Department of Cardiology, Bakirkoy Dr. Sadi Konuk Education and Research Hospital, Istanbul, Turkey
- Murat Koser — Department of Biochemistry, Silivri State Hospital, Istanbul, Turkey
- Nursel Kocamaz — Department of İnternal Medicine, Bakirkoy Dr. Sadi Konuk Education and Research Hospital, Istanbul, Turkey
Keywords
myocardial infarction, presepsin, inflammation, atherosclerosis
DOI
https://doi.org/10.15836/ccar2016.524Full Text
**Background:** Acute myocardial infarction (AMI) could be considered to be a state of inflammation. Many inflammatory markers have been evaluated during AMI setting so far. Presepsin (PSP) is a novel biomarker for diagnosis and prognosis of systemic inflammation that have not been studied in AMI setting up to date. In this study, we aimed to examine serum PSP levels in patients with acute ST elevation myocardial infarction (STEMI). **Patients and Methods:** 48 patients with STEMI and fifty healthy controls without coronary artery disease, verified by coronary angiography, were included in the study. Together with routine laboratory tests needed for STEMI, plasma concentrations of PSP were measured in peripheral venous blood samples of the participants. **Results:** Plasma PSP and troponin levels were significantly higher in patients with STEMI than controls (1988.89±3101.55 vs 914.22±911.35 pg/mL, p=0.001 and 3.46±3.39 vs 0.08±0.43 ng/mL, p=0.001, respectively). Cut-off value for PSP was found 447 pg/ml to detect STEMI with 87.5%, sensitivity, 44% specificity, 60% positive predictive value and 78.5% negative predictive value. **Conclusions:** In this study, PSP levels were found significantly elevated in patients with STEMI together with high sensitive troponins. PSP may be a new marker for AMI detection. Large scale studies are needed to reveal the importance of PSP in the diagnosis of AMI.