85岁老人脑脊液中tau蛋白和泛素的人群研究:与痴呆和脑萎缩的严重程度有关,但与载脂蛋白E4等位基因无关

Skoog I. , Vanmechelen E. , Andreasson L.A. , Palmertz B. , Davidsson P. , Hesse C. , Blennow K.
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引用次数: 78

摘要

阿尔茨海默病(AD)是最常见的痴呆症形式,其特征是神经元及其突触的退化,与同年龄的非痴呆个体相比,老年斑(SP)和神经原纤维缠结(NFT)的数量更多。NFT由过度磷酸化和泛素化形式的tau蛋白组成。先前的研究发现,AD患者脑脊液中tau和泛素均升高。我们在85岁的人群样本中检测了CSF-tau和csf -泛素,26名痴呆(11名可能患有阿尔茨海默病(AD), 13名可能患有血管性痴呆(VAD), 2名患有混合型(AD/VAD)痴呆)和35名非痴呆个体。CSF-tau在可能AD组(254±113 pg/mL;P<0.01)和可能VAD组(247±75 pg/mL;P<0.005)均显著高于非痴呆组(171±78 pg/mL),但在可能AD组和可能VAD组之间无显著差异。相比之下,csf -泛素在可能AD组(100±24 ng/mL)、可能VAD组(102±16 ng/mL)和非痴呆组(97±27 ng/mL)之间无显著差异。CSF-tau随着痴呆严重程度的增加而增加(P<0.001),但在csf -泛素中没有发现这种关系。在携带或不携带载脂蛋白E4亚型的患者中,CSF-tau和csf -泛素均无差异。计算机断层扫描显示,较高的CSF-tau和csf -泛素水平也与皮质和中枢脑萎缩程度增加有关。CSF-tau与痴呆严重程度和脑萎缩之间的关系表明,CSF-tau可用于衡量痴呆患者的神经元/轴突变性。我们之前的研究显示,在年轻AD和VAD患者中,CSF-tau和csf -泛素水平均显著升高。老年患者中CSF-tau蛋白的不太明显的增加和csf -泛素的缺乏差异表明,老年痴呆患者退行性过程的严重程度低于年轻痴呆患者。
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A Population-based Study of tau Protein and Ubiquitin in Cerebrospinal Fluid in 85-year-olds: Relation to Severity of Dementia and Cerebral Atrophy, but not to the Apolipoprotein E4 Allele
Alzheimer's disease (AD) is the most common form of dementia, and is characterized by a degeneration of neurones and their synapses, and a higher number of senile plaques (SP) and neurofibrillary tangles (NFT) compared with that found in non-demented individuals of the same age. NFT are composed of a hyperphosphorylated and ubiquitinated form of tau protein. Previous studies have found that in the cerebrospinal fluid (CSF) both tau and ubiquitin are increased in AD. We examined CSF-tau and CSF-ubiquitin in a population based sample of 85-year-olds, 26 demented (11 with probable Alzheimer's disease (AD), 13 with probable vascular dementia (VAD) and 2 with mixed (AD/VAD) type of dementia) and 35 non-demented individuals. CSF-tau was significantly higher both in the probable AD group (254 +/- 113 pg/mL; P < 0.01), and in the probable VAD group (247 +/- 75 pg/mL; P < 0.005), than in the non-demented group (171 +/- 78 pg/mL), but did not significantly differ between the probable AD and probable VAD groups. In contrast, CSF-ubiquitin did not significantly differ between the probable AD (100 +/- 24 ng/mL), probable VAD (102 +/- 16 ng/mL), and non-demented (97 +/- 27 ng/mL) groups. CSF-tau increased with increasing severity of dementia (P < 0.001), though no such relation was found for CSF-ubiquitin. Neither CSF-tau nor CSF-ubiquitin differed between patients with or without the apolipoprotein E E4 isoform. Higher CSF-tau and CSF-ubiquitin levels were also associated with increasing degree of cortical and central brain atrophy as measured by computerized tomography. The relationships between CSF-tau and severity of dementia and to brain atrophy suggest that CSF-tau may be used as a measure of neuronal/axonal degeneration in patients with dementia. We have previously shown a marked increase in both CSF-tau and CSF-ubiquitin in younger patients with AD and VAD. The less pronounced increase in CSF-tau and the lack of difference in CSF-ubiquitin in older patients suggest that the severity of the degenerative process is less in older than in younger demented patients.
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