Association of dimethylarginines and mediators of inflammation after acute ischemic stroke

<p>Abstract</p> <p>Background</p> <p>Elevated levels of asymmetric dimethylarginine (ADMA) and symmetric dimethylarginine (SDMA) are accompanied by endothelial dysfunction and predict adverse outcome after ischemic stroke. Via induction of oxidative stress, dimethylargi...

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Main Authors: Chen Shufen, Martens-Lobenhoffer Jens, Weissenborn Karin, Kielstein Jan T, Lichtinghagen Ralf, Deb Milani, Li Na, Tryc Anita B, Goldbecker Annemarie, Dong Qiang, Bode-Böger Stefanie M, Worthmann Hans
Format: Article
Language:English
Published: BMC 2012-11-01
Series:Journal of Neuroinflammation
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Online Access:http://www.jneuroinflammation.com/content/9/1/251
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author Chen Shufen
Martens-Lobenhoffer Jens
Weissenborn Karin
Kielstein Jan T
Lichtinghagen Ralf
Deb Milani
Li Na
Tryc Anita B
Goldbecker Annemarie
Dong Qiang
Bode-Böger Stefanie M
Worthmann Hans
author_facet Chen Shufen
Martens-Lobenhoffer Jens
Weissenborn Karin
Kielstein Jan T
Lichtinghagen Ralf
Deb Milani
Li Na
Tryc Anita B
Goldbecker Annemarie
Dong Qiang
Bode-Böger Stefanie M
Worthmann Hans
author_sort Chen Shufen
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>Elevated levels of asymmetric dimethylarginine (ADMA) and symmetric dimethylarginine (SDMA) are accompanied by endothelial dysfunction and predict adverse outcome after ischemic stroke. Via induction of oxidative stress, dimethylarginines are possibly linked to the inflammatory cascade after stroke that is known to considerably contribute to secondary progression of brain injury. We sought to investigate the association between dimethylarginines and inflammatory mediators in patients with acute ischemic stroke.</p> <p>Methods</p> <p>Plasma levels of ADMA and SDMA were measured in prospectively collected blood samples of 58 patients with acute ischemic stroke. Blood samples were taken at 6 hours, 12 hours, 24 hours, 3 days and 7 days after onset of symptoms. Analyses of ADMA and SDMA were done by high-performance liquid chromatography-tandem mass spectrometry. Monocyte chemotactic protein-1 (MCP-1), matrix metalloproteinase-9 (MMP-9), tissue inhibitor of matrix metalloproteinase-1 (TIMP-1), interleukin-6 (IL-6), C-reactive protein (CRP) and S100B as markers of inflammation and brain damage were determined by commercially available immunometric assays. Patient data were compared with control data from 32 age-adjusted healthy volunteers. Baseline stroke severity was evaluated by the National Institutes of Health Stroke Scale (NIHSS) (NIHSS 0 to 1: mild stroke; NIHSS 2 to 8: moderate stroke; NIHSS ≥9: severe stroke).</p> <p>Results</p> <p>Plasma ADMA and SDMA levels significantly correlated with blood levels of inflammatory mediators up to day 7 after stroke. On multiple stepwise linear regression analysis ADMA correlated with TIMP-1 at 6 hours, 24 hours, 3 days and 7 days, MMP-9 at 12 hours and IL-6 at 7 days (<it>P</it> <0.05) while SDMA correlated with MCP-1 at 6 hours, 24 hours, 3 days and 7 days as well as IL-6 at 3 days and 7 days (<it>P</it> <0.05).</p> <p>Conclusions</p> <p>The levels of the vasoactive compound ADMA as well as levels of its structural isomer SDMA are associated with levels of inflammatory mediators after acute ischemic stroke. Further studies need to elucidate the cause and effect relationship of these crucial players.</p>
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spelling doaj.art-5868101c036143a08881b45a707884cf2022-12-21T21:03:51ZengBMCJournal of Neuroinflammation1742-20942012-11-019125110.1186/1742-2094-9-251Association of dimethylarginines and mediators of inflammation after acute ischemic strokeChen ShufenMartens-Lobenhoffer JensWeissenborn KarinKielstein Jan TLichtinghagen RalfDeb MilaniLi NaTryc Anita BGoldbecker AnnemarieDong QiangBode-Böger Stefanie MWorthmann Hans<p>Abstract</p> <p>Background</p> <p>Elevated levels of asymmetric dimethylarginine (ADMA) and symmetric dimethylarginine (SDMA) are accompanied by endothelial dysfunction and predict adverse outcome after ischemic stroke. Via induction of oxidative stress, dimethylarginines are possibly linked to the inflammatory cascade after stroke that is known to considerably contribute to secondary progression of brain injury. We sought to investigate the association between dimethylarginines and inflammatory mediators in patients with acute ischemic stroke.</p> <p>Methods</p> <p>Plasma levels of ADMA and SDMA were measured in prospectively collected blood samples of 58 patients with acute ischemic stroke. Blood samples were taken at 6 hours, 12 hours, 24 hours, 3 days and 7 days after onset of symptoms. Analyses of ADMA and SDMA were done by high-performance liquid chromatography-tandem mass spectrometry. Monocyte chemotactic protein-1 (MCP-1), matrix metalloproteinase-9 (MMP-9), tissue inhibitor of matrix metalloproteinase-1 (TIMP-1), interleukin-6 (IL-6), C-reactive protein (CRP) and S100B as markers of inflammation and brain damage were determined by commercially available immunometric assays. Patient data were compared with control data from 32 age-adjusted healthy volunteers. Baseline stroke severity was evaluated by the National Institutes of Health Stroke Scale (NIHSS) (NIHSS 0 to 1: mild stroke; NIHSS 2 to 8: moderate stroke; NIHSS ≥9: severe stroke).</p> <p>Results</p> <p>Plasma ADMA and SDMA levels significantly correlated with blood levels of inflammatory mediators up to day 7 after stroke. On multiple stepwise linear regression analysis ADMA correlated with TIMP-1 at 6 hours, 24 hours, 3 days and 7 days, MMP-9 at 12 hours and IL-6 at 7 days (<it>P</it> <0.05) while SDMA correlated with MCP-1 at 6 hours, 24 hours, 3 days and 7 days as well as IL-6 at 3 days and 7 days (<it>P</it> <0.05).</p> <p>Conclusions</p> <p>The levels of the vasoactive compound ADMA as well as levels of its structural isomer SDMA are associated with levels of inflammatory mediators after acute ischemic stroke. Further studies need to elucidate the cause and effect relationship of these crucial players.</p>http://www.jneuroinflammation.com/content/9/1/251Asymmetric dimethylarginine (ADMA)Symmetric dimethylarginine (SDMA)StrokeInflammation
spellingShingle Chen Shufen
Martens-Lobenhoffer Jens
Weissenborn Karin
Kielstein Jan T
Lichtinghagen Ralf
Deb Milani
Li Na
Tryc Anita B
Goldbecker Annemarie
Dong Qiang
Bode-Böger Stefanie M
Worthmann Hans
Association of dimethylarginines and mediators of inflammation after acute ischemic stroke
Journal of Neuroinflammation
Asymmetric dimethylarginine (ADMA)
Symmetric dimethylarginine (SDMA)
Stroke
Inflammation
title Association of dimethylarginines and mediators of inflammation after acute ischemic stroke
title_full Association of dimethylarginines and mediators of inflammation after acute ischemic stroke
title_fullStr Association of dimethylarginines and mediators of inflammation after acute ischemic stroke
title_full_unstemmed Association of dimethylarginines and mediators of inflammation after acute ischemic stroke
title_short Association of dimethylarginines and mediators of inflammation after acute ischemic stroke
title_sort association of dimethylarginines and mediators of inflammation after acute ischemic stroke
topic Asymmetric dimethylarginine (ADMA)
Symmetric dimethylarginine (SDMA)
Stroke
Inflammation
url http://www.jneuroinflammation.com/content/9/1/251
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