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Serum cytokine and glucose levels as predictors of poststroke fatigue in acute ischemic stroke patients
Fatigue is a common but often overlooked symptom after stroke. This study investigated whether stroke type, infarct volume, and laterality, as well as the levels of various cytokines and other blood components in the acute phase of acute ischemic stroke (AIS), can predict the level of fatigue at 6,...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Springer-Verlag
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3065647/ https://www.ncbi.nlm.nih.gov/pubmed/21365457 http://dx.doi.org/10.1007/s00415-011-5962-8 |
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author | Ormstad, Heidi Aass, Hans Christian Dalsbotten Amthor, Karl-Friedrich Lund-Sørensen, Niels Sandvik, Leiv |
author_facet | Ormstad, Heidi Aass, Hans Christian Dalsbotten Amthor, Karl-Friedrich Lund-Sørensen, Niels Sandvik, Leiv |
author_sort | Ormstad, Heidi |
collection | PubMed |
description | Fatigue is a common but often overlooked symptom after stroke. This study investigated whether stroke type, infarct volume, and laterality, as well as the levels of various cytokines and other blood components in the acute phase of acute ischemic stroke (AIS), can predict the level of fatigue at 6, 12, and 18 months after its onset. In 45 patients with acute stroke, serum levels of C-reactive protein, hemoglobin, glucose, and 13 cytokines were measured within 72 h of stroke onset. The cytokine measurements were performed using BioPlex XMap technology (Luminex). The acute serum levels of interleukin (IL)-1β and glucose were positively correlated with the score on the Fatigue Severity Scale (FSS) at 6 months after the stroke (r = 0.37, p = 0.015, and r = 0.37, p = 0.017, respectively). The acute serum levels of IL-ra and IL-9 were negatively correlated with FSS score at 12 months after the stroke (r = −0.38, p = 0.013, and r = −0.36, p = 0.019, respectively). The FSS score at 12 months after stroke was significantly lower in patients with radiologically confirmed infarction than in those without such confirmation (p = 0.048). The FSS score at 18 months was not correlated with any of the measured variables. High acute serum levels of glucose and IL-1β, and low IL1-ra and IL-9 may predict fatigue after AIS, indicating that the development of poststroke fatigue can be accounted for by the proinflammatory response associated with AIS. These novel findings support a new cytokine theory of fatigue after stroke. However, more research is needed to validate the results of this study. |
format | Text |
id | pubmed-3065647 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-30656472011-04-21 Serum cytokine and glucose levels as predictors of poststroke fatigue in acute ischemic stroke patients Ormstad, Heidi Aass, Hans Christian Dalsbotten Amthor, Karl-Friedrich Lund-Sørensen, Niels Sandvik, Leiv J Neurol Original Communication Fatigue is a common but often overlooked symptom after stroke. This study investigated whether stroke type, infarct volume, and laterality, as well as the levels of various cytokines and other blood components in the acute phase of acute ischemic stroke (AIS), can predict the level of fatigue at 6, 12, and 18 months after its onset. In 45 patients with acute stroke, serum levels of C-reactive protein, hemoglobin, glucose, and 13 cytokines were measured within 72 h of stroke onset. The cytokine measurements were performed using BioPlex XMap technology (Luminex). The acute serum levels of interleukin (IL)-1β and glucose were positively correlated with the score on the Fatigue Severity Scale (FSS) at 6 months after the stroke (r = 0.37, p = 0.015, and r = 0.37, p = 0.017, respectively). The acute serum levels of IL-ra and IL-9 were negatively correlated with FSS score at 12 months after the stroke (r = −0.38, p = 0.013, and r = −0.36, p = 0.019, respectively). The FSS score at 12 months after stroke was significantly lower in patients with radiologically confirmed infarction than in those without such confirmation (p = 0.048). The FSS score at 18 months was not correlated with any of the measured variables. High acute serum levels of glucose and IL-1β, and low IL1-ra and IL-9 may predict fatigue after AIS, indicating that the development of poststroke fatigue can be accounted for by the proinflammatory response associated with AIS. These novel findings support a new cytokine theory of fatigue after stroke. However, more research is needed to validate the results of this study. Springer-Verlag 2011-03-02 2011 /pmc/articles/PMC3065647/ /pubmed/21365457 http://dx.doi.org/10.1007/s00415-011-5962-8 Text en © The Author(s) 2011 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Original Communication Ormstad, Heidi Aass, Hans Christian Dalsbotten Amthor, Karl-Friedrich Lund-Sørensen, Niels Sandvik, Leiv Serum cytokine and glucose levels as predictors of poststroke fatigue in acute ischemic stroke patients |
title | Serum cytokine and glucose levels as predictors of poststroke fatigue in acute ischemic stroke patients |
title_full | Serum cytokine and glucose levels as predictors of poststroke fatigue in acute ischemic stroke patients |
title_fullStr | Serum cytokine and glucose levels as predictors of poststroke fatigue in acute ischemic stroke patients |
title_full_unstemmed | Serum cytokine and glucose levels as predictors of poststroke fatigue in acute ischemic stroke patients |
title_short | Serum cytokine and glucose levels as predictors of poststroke fatigue in acute ischemic stroke patients |
title_sort | serum cytokine and glucose levels as predictors of poststroke fatigue in acute ischemic stroke patients |
topic | Original Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3065647/ https://www.ncbi.nlm.nih.gov/pubmed/21365457 http://dx.doi.org/10.1007/s00415-011-5962-8 |
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