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Presepsin (sCD14-ST): could it be a novel marker for the diagnosis of ST elevation myocardial infarction?
INTRODUCTION: Acute myocardial infarction (AMI) could be considered to be a state of inflammation. Many inflammatory markers have been evaluated in the AMI setting so far. Presepsin (PSP) is a novel biomarker for diagnosis and prognosis of systemic inflammation that has not been studied in the AMI s...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Termedia Publishing House
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5596112/ https://www.ncbi.nlm.nih.gov/pubmed/28905041 http://dx.doi.org/10.5114/amsad.2017.66827 |
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author | Caglar, Fatma Nihan Turhan Isiksacan, Nilgun Biyik, Ismail Opan, Selcuk Cebe, Hulya Akturk, Ibrahim Faruk |
author_facet | Caglar, Fatma Nihan Turhan Isiksacan, Nilgun Biyik, Ismail Opan, Selcuk Cebe, Hulya Akturk, Ibrahim Faruk |
author_sort | Caglar, Fatma Nihan Turhan |
collection | PubMed |
description | INTRODUCTION: Acute myocardial infarction (AMI) could be considered to be a state of inflammation. Many inflammatory markers have been evaluated in the AMI setting so far. Presepsin (PSP) is a novel biomarker for diagnosis and prognosis of systemic inflammation that has not been studied in the AMI setting to date. In this study, we aimed to examine serum PSP levels in patients with acute ST elevation myocardial infarction (STEMI). MATERIAL AND METHODS: Forty-eight 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). The cut-off value for PSP of 447 pg/ml was found 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 to be significantly elevated in patients with STEMI together with high-sensitivity troponins. The PSP may be a new marker for AMI detection. Large scale studies are needed to reveal the importance of PSP in the diagnosis and prognosis of AMI. |
format | Online Article Text |
id | pubmed-5596112 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Termedia Publishing House |
record_format | MEDLINE/PubMed |
spelling | pubmed-55961122017-09-13 Presepsin (sCD14-ST): could it be a novel marker for the diagnosis of ST elevation myocardial infarction? Caglar, Fatma Nihan Turhan Isiksacan, Nilgun Biyik, Ismail Opan, Selcuk Cebe, Hulya Akturk, Ibrahim Faruk Arch Med Sci Atheroscler Dis Clinical Research INTRODUCTION: Acute myocardial infarction (AMI) could be considered to be a state of inflammation. Many inflammatory markers have been evaluated in the AMI setting so far. Presepsin (PSP) is a novel biomarker for diagnosis and prognosis of systemic inflammation that has not been studied in the AMI setting to date. In this study, we aimed to examine serum PSP levels in patients with acute ST elevation myocardial infarction (STEMI). MATERIAL AND METHODS: Forty-eight 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). The cut-off value for PSP of 447 pg/ml was found 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 to be significantly elevated in patients with STEMI together with high-sensitivity troponins. The PSP may be a new marker for AMI detection. Large scale studies are needed to reveal the importance of PSP in the diagnosis and prognosis of AMI. Termedia Publishing House 2017-03-27 /pmc/articles/PMC5596112/ /pubmed/28905041 http://dx.doi.org/10.5114/amsad.2017.66827 Text en Copyright: © 2017 Termedia & Banach http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license. |
spellingShingle | Clinical Research Caglar, Fatma Nihan Turhan Isiksacan, Nilgun Biyik, Ismail Opan, Selcuk Cebe, Hulya Akturk, Ibrahim Faruk Presepsin (sCD14-ST): could it be a novel marker for the diagnosis of ST elevation myocardial infarction? |
title | Presepsin (sCD14-ST): could it be a novel marker for the diagnosis of ST elevation myocardial infarction? |
title_full | Presepsin (sCD14-ST): could it be a novel marker for the diagnosis of ST elevation myocardial infarction? |
title_fullStr | Presepsin (sCD14-ST): could it be a novel marker for the diagnosis of ST elevation myocardial infarction? |
title_full_unstemmed | Presepsin (sCD14-ST): could it be a novel marker for the diagnosis of ST elevation myocardial infarction? |
title_short | Presepsin (sCD14-ST): could it be a novel marker for the diagnosis of ST elevation myocardial infarction? |
title_sort | presepsin (scd14-st): could it be a novel marker for the diagnosis of st elevation myocardial infarction? |
topic | Clinical Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5596112/ https://www.ncbi.nlm.nih.gov/pubmed/28905041 http://dx.doi.org/10.5114/amsad.2017.66827 |
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