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首页> 外文期刊>Neurological Research >Elevation of MCP-1 and MCP-1/VEGF ratio in cerebrospinal fluid of amyotrophic lateral sclerosis patients
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Elevation of MCP-1 and MCP-1/VEGF ratio in cerebrospinal fluid of amyotrophic lateral sclerosis patients

机译:肌萎缩性侧索硬化症患者脑脊液中MCP-1和MCP-1 / VEGF的升高

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摘要

Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease with progressive cell death of upper and lower motor neurons. In this study, we measured monocyte chemotactic protein-1 (MCP-1) and vascular endothelial growth factor (VEGF) levels in cerebrospinal fluid (CSF) and serum by enzyme-linked immunosorbent assay (ELISA) in 42 ALS patients, and compared these levels with those of control subjects with other neurodegenerative disorders or with those of normal controls. MCP-1 levels in CSF were significantly higher in ALS patients than in the control group. VEGF levels in CSF tended to be lower in ALS patients than in the control group, but not significantly. A positive correlation was found between MCP-1 levels in CSF of ALS patients and the total Norris scale. The elevation of MCP-1/VEGF ratio in CSF was more specific to ALS patients compared to other neurological diseases such as Parkinson's disease (PD) and spinocerebellar ataxia (SCA) and to controls. Our data suggested that both MCP-1 levels and MCP-1/VEGF ratio in CSF may be useful markers for the clinical diagnosis of ALS.
机译:肌萎缩性侧索硬化症(ALS)是一种神经退行性疾病,伴有上,下运动神经元的进行性细胞死亡。在这项研究中,我们通过酶联免疫吸附法(ELISA)测定了42例ALS患者的脑脊液(CSF)和血清中单核细胞趋化蛋白1(MCP-1)和血管内皮生长因子(VEGF)的水平,并进行了比较与患有其他神经退行性疾病的对照组或正常对照组的水平比较。 ALS患者的CSF中MCP-1水平显着高于对照组。 ALS患者中CSF​​中的VEGF水平倾向于低于对照组,但不显着。发现ALS患者脑脊液中MCP-1水平与总诺里斯量表之间呈正相关。与其他神经系统疾病(例如帕金森氏病(PD)和脊髓小脑共济失调(SCA))和对照组相比,CSF中MCP-1 / VEGF比值的升高对ALS患者更具特异性。我们的数据表明,脑脊液中的MCP-1水平和MCP-1 / VEGF比可能是ALS临床诊断的有用标志。

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  • 来源
    《Neurological Research》 |2007年第8期|772-776|共5页
  • 作者单位

    Department of Neurology, Graduate School of Medicine and Dentistry, Okayama University, Okayama, Japan;

    Department of Neurology, Graduate School of Medicine and Dentistry, Okayama University, Okayama, Japan;

    Department of Neurology, Graduate School of Medicine and Dentistry, Okayama University, Okayama, Japan;

    Department of Neurology, Graduate School of Medicine and Dentistry, Okayama University, Okayama, Japan;

    Department of Neurology, Graduate School of Medicine and Dentistry, Okayama University, Okayama, Japan;

    Department of Neurology, Graduate School of Medicine and Dentistry, Okayama University, Okayama, Japan;

    Department of Neurology, Graduate School of Medicine and Dentistry, Okayama University, Okayama, Japan;

    Department of Neurology, Graduate School of Medicine and Dentistry, Okayama University, Okayama, Japan;

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