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Detection of Soluble Amyloid-β Oligomers and Insoluble High-Molecular-Weight Particles in CSF: Development of Methods with Potential for Diagnosis and Therapy Monitoring of Alzheimer's Disease

机译:脑脊液中可溶性淀粉样β低聚物和不溶性高分子量颗粒的检测:可能诊断和治疗阿尔茨海默氏病的方法的发展

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摘要

The diagnosis of probable Alzheimer's disease (AD) can be established premortem based on clinical criteria like neuropsychological tests. Post mortem, specific neuropathological changes like amyloid plaques define AD. However, the standard criteria based on medical history and mental status examinations do not take into account the long preclinical features of the disease, and a biomarker for improved diagnosis of AD is urgently needed. In a large number of studies, amyloid-β (Aβ) monomer concentrations in CSF of AD patients are consistently and significantly reduced when compared to healthy controls. Therefore, monomeric Aβ in CSF was suggested to be a helpful biomarker for the diagnosis of preclinical AD. However, not the monomeric form, but Aβ oligomers have been shown to be the toxic species in AD pathology, and their quantification and characterization could facilitate AD diagnosis and therapy monitoring. Here, we review the current status of assay development to reliably and routinely detect Aβ oligomers and high-molecular-weight particles in CSF.
机译:可以根据临床标准(例如神经心理学测试)来确定死前诊断可能的阿尔茨海默氏病(AD)。验尸后,特定的神经病理变化(如淀粉样斑块)定义了AD。但是,基于病史和精神状态检查的标准标准并未考虑到该疾病的长期临床前特征,因此迫切需要一种用于改善AD诊断的生物标记物。在大量研究中,与健康对照组相比,AD患者CSF中的淀粉样β(Aβ)单体浓度持续且显着降低。因此,CSF中的单体Aβ被认为是诊断临床前AD的有用生物标志物。然而,已经证明,Aβ寡聚体不是单体形式,而是Aβ病理学中的有毒物质,其定量和表征可以促进AD诊断和治疗监测。在此,我们回顾了检测开发的现状,以可靠,常规地检测CSF中的Aβ低聚物和高分子量颗粒。

著录项

  • 作者

    Funke, Susanne Aileen;

  • 作者单位
  • 年度 2011
  • 总页数
  • 原文格式 PDF
  • 正文语种 {"code":"en","name":"English","id":9}
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