Bjerke Maria, Jonsson Michael, Nordlund Arto, Eckerström Carl, Blennow Kaj, Zetterberg Henrik, Pantoni Leonardo, Inzitari Domenico, Schmidt Reinhold, Wallin Anders
Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry, The Sahlgrenska Academy at the University of Gothenburg, Mölndal, Sweden.
Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry, The Sahlgrenska Academy at the University of Gothenburg, Mölndal, Sweden ; UCL Institute of Neurology, London, UK.
Dement Geriatr Cogn Dis Extra. 2014 Oct 21;4(3):385-94. doi: 10.1159/000366119. eCollection 2014 Sep.
Small vessel disease (SVD) represents a common often progressive condition in elderly people contributing to cognitive disability. The relationship between cerebrospinal fluid (CSF) biomarkers and imaging correlates of SVD was investigated, and the findings were hypothesized to be associated with a neuropsychological profile of SVD.
CSF SVD-related biomarkers [neurofilament light (NF-L), myelin basic protein (MBP), soluble amyloid precursor protein-β (sAPPβ), matrix metalloproteinases (MMPs), and tissue inhibitor of metalloproteinase (TIMP)] were analysed in 46 non-demented elderly with imaging findings of SVD. We assessed the relationship between the CSF biomarkers and white matter hyperintensity (WMH) volume, diffusion-weighted imaging and atrophy as well as their association with neuropsychological profiles.
The WMH volume correlated with ventricular dilation, which was associated with executive function and speed and attention. Increased WMH and ventricular dilation were related to increased CSF levels of TIMP-1, NF-L and MBP and to decreased sAPPβ. A positive correlation was found between the CSF biomarker MMP-9 and WMH progression.
The link between progressive WMH and MMP-9 suggests an involvement of the enzyme in white matter degeneration. CSF TIMP-1, NF-L, MBP and sAPPβ may function as biological markers of white matter damage.
小血管疾病(SVD)是老年人常见的、通常呈进行性发展的疾病,可导致认知障碍。本研究调查了脑脊液(CSF)生物标志物与SVD影像学相关指标之间的关系,并假设这些结果与SVD的神经心理学特征相关。
对46例无痴呆的老年人进行分析,这些老年人具有SVD的影像学表现,并检测其脑脊液中与SVD相关的生物标志物[神经丝轻链(NF-L)、髓鞘碱性蛋白(MBP)、可溶性淀粉样前体蛋白-β(sAPPβ)、基质金属蛋白酶(MMPs)和金属蛋白酶组织抑制剂(TIMP)]。我们评估了脑脊液生物标志物与白质高信号(WMH)体积、弥散加权成像及萎缩之间的关系,以及它们与神经心理学特征的相关性。
WMH体积与脑室扩张相关,而脑室扩张与执行功能、速度和注意力有关。WMH增加和脑室扩张与脑脊液中TIMP-1、NF-L和MBP水平升高以及sAPPβ水平降低有关。脑脊液生物标志物MMP-9与WMH进展呈正相关。
进行性WMH与MMP-9之间的联系表明该酶参与了白质变性。脑脊液TIMP-1、NF-L、MBP和sAPPβ可能作为白质损伤的生物学标志物。