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Association of dimethylarginines and mediators of inflammation after acute ischemic stroke

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机构: [1]Hannover Med Sch, Dept Neurol, D-30623 Hannover, Germany; [2]Fudan Univ, Huashan Hosp, Dept Neurol, Shanghai 200040, Peoples R China; [3]Univ Magdeburg, Univ Hosp, Dept Clin Pharmacol, D-39120 Magdeburg, Germany; [4]Ctr Syst Neurosci ZSN, D-30559 Hannover, Germany; [5]Hannover Med Sch, Dept Nephrol & Hypertens, D-30623 Hannover, Germany; [6]Hannover Med Sch, Dept Clin Chem, D-30623 Hannover, Germany; [7]Capital Med Univ, Beijing Tiantan Hosp, Dept Neurol, Beijing 100050, Peoples R China; [8]Hannover Med Sch, Dept Neurol, Carl Neuberg Str 1, D-30623 Hannover, Germany
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关键词: Asymmetric dimethylarginine (ADMA) Symmetric dimethylarginine (SDMA) Stroke Inflammation

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Background: 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. Methods: 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). Results: 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 (P < 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 (P < 0.05). Conclusions: 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.

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出版当年[2011]版:
大类 | 2 区 医学
小类 | 2 区 神经科学
最新[2025]版:
大类 | 1 区 医学
小类 | 1 区 免疫学 1 区 神经科学
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出版当年[2010]版:
Q1 NEUROSCIENCES
最新[2023]版:
Q1 IMMUNOLOGY Q1 NEUROSCIENCES

影响因子: 最新[2023版] 最新五年平均 出版当年[2010版] 出版当年五年平均 出版前一年[2009版] 出版后一年[2011版]

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第一作者机构: [1]Hannover Med Sch, Dept Neurol, D-30623 Hannover, Germany; [2]Fudan Univ, Huashan Hosp, Dept Neurol, Shanghai 200040, Peoples R China;
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通讯机构: [1]Hannover Med Sch, Dept Neurol, D-30623 Hannover, Germany; [8]Hannover Med Sch, Dept Neurol, Carl Neuberg Str 1, D-30623 Hannover, Germany
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