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Levels of brain natriuretic peptide as a marker for the diagnosis and prognosis of acute ischemic stroke
INTRODUCTION: The relationships between plasma levels of brain natriuretic peptide (BNP) and severity and location of stroke, prognosis, and infarct volume were investigated in acute ischemic stroke patients who presented within the first 24 hours (h) of stroke. MATERIAL AND METHODS: Brain natriuret...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Termedia Publishing House
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5421533/ https://www.ncbi.nlm.nih.gov/pubmed/28905014 http://dx.doi.org/10.5114/amsad.2016.59751 |
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author | Sayan, Saadet Kotan, Dilcan |
author_facet | Sayan, Saadet Kotan, Dilcan |
author_sort | Sayan, Saadet |
collection | PubMed |
description | INTRODUCTION: The relationships between plasma levels of brain natriuretic peptide (BNP) and severity and location of stroke, prognosis, and infarct volume were investigated in acute ischemic stroke patients who presented within the first 24 hours (h) of stroke. MATERIAL AND METHODS: Brain natriuretic peptide levels were tested in 40 patients and 30 healthy controls. Infarct volume was automatically calculated by multi-slice computed tomography. Disease severity was assessed using the National Institutes of Health Stroke Scale (NIHSS) at presentation, 24 h, 72 h and the 28(th) day. Progression was defined as an increase of more than two points in the NIHSS scores. RESULTS: The mean BNP levels were 284.16 ±382.79 at presentation and 273.78 ±451.91 at 72 h in the patient group, whereas the mean BNP level was 25.29 ±13.47 in controls. There was a statistically significant difference between the two groups (p < 0.001). Differences in BNP levels among patient subgroups according to the TOAST and OCSP classifications were not statistically significant (p = 0.534, p = 0.943, respectively). There was no significant correlation between plasma BNP level and infarct volume or NIHSS scores (p = 0.5, p = 0.07). A positive correlation was found between BNP levels and the length of the hospitalization period (p = 0.03 and r = 0.33). There was no statistically significant relationship between elevated plasma BNP levels and progression of disease (p = 0.08). CONCLUSIONS: Plasma BNP levels were increased in the acute phase of stroke; therefore, BNP could be used as a biomarker for morbidity and mortality, even in patients without cardiac failure. |
format | Online Article Text |
id | pubmed-5421533 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Termedia Publishing House |
record_format | MEDLINE/PubMed |
spelling | pubmed-54215332017-09-13 Levels of brain natriuretic peptide as a marker for the diagnosis and prognosis of acute ischemic stroke Sayan, Saadet Kotan, Dilcan Arch Med Sci Atheroscler Dis Clinical Research INTRODUCTION: The relationships between plasma levels of brain natriuretic peptide (BNP) and severity and location of stroke, prognosis, and infarct volume were investigated in acute ischemic stroke patients who presented within the first 24 hours (h) of stroke. MATERIAL AND METHODS: Brain natriuretic peptide levels were tested in 40 patients and 30 healthy controls. Infarct volume was automatically calculated by multi-slice computed tomography. Disease severity was assessed using the National Institutes of Health Stroke Scale (NIHSS) at presentation, 24 h, 72 h and the 28(th) day. Progression was defined as an increase of more than two points in the NIHSS scores. RESULTS: The mean BNP levels were 284.16 ±382.79 at presentation and 273.78 ±451.91 at 72 h in the patient group, whereas the mean BNP level was 25.29 ±13.47 in controls. There was a statistically significant difference between the two groups (p < 0.001). Differences in BNP levels among patient subgroups according to the TOAST and OCSP classifications were not statistically significant (p = 0.534, p = 0.943, respectively). There was no significant correlation between plasma BNP level and infarct volume or NIHSS scores (p = 0.5, p = 0.07). A positive correlation was found between BNP levels and the length of the hospitalization period (p = 0.03 and r = 0.33). There was no statistically significant relationship between elevated plasma BNP levels and progression of disease (p = 0.08). CONCLUSIONS: Plasma BNP levels were increased in the acute phase of stroke; therefore, BNP could be used as a biomarker for morbidity and mortality, even in patients without cardiac failure. Termedia Publishing House 2016-05-09 /pmc/articles/PMC5421533/ /pubmed/28905014 http://dx.doi.org/10.5114/amsad.2016.59751 Text en Copyright: © 2016 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 Sayan, Saadet Kotan, Dilcan Levels of brain natriuretic peptide as a marker for the diagnosis and prognosis of acute ischemic stroke |
title | Levels of brain natriuretic peptide as a marker for the diagnosis and prognosis of acute ischemic stroke |
title_full | Levels of brain natriuretic peptide as a marker for the diagnosis and prognosis of acute ischemic stroke |
title_fullStr | Levels of brain natriuretic peptide as a marker for the diagnosis and prognosis of acute ischemic stroke |
title_full_unstemmed | Levels of brain natriuretic peptide as a marker for the diagnosis and prognosis of acute ischemic stroke |
title_short | Levels of brain natriuretic peptide as a marker for the diagnosis and prognosis of acute ischemic stroke |
title_sort | levels of brain natriuretic peptide as a marker for the diagnosis and prognosis of acute ischemic stroke |
topic | Clinical Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5421533/ https://www.ncbi.nlm.nih.gov/pubmed/28905014 http://dx.doi.org/10.5114/amsad.2016.59751 |
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