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脑脊液神经丝蛋白水平在散发型克雅氏病中升高。

CSF neurofilament proteins levels are elevated in sporadic Creutzfeldt-Jakob disease.

机构信息

Department of Neurology, Radboud University Nijmegen Medical Centre, Donders Institute for Brain, Cognition and Behaviour, Alzheimer Centre Nijmegen, The Netherlands.

出版信息

J Alzheimers Dis. 2010;21(2):569-76. doi: 10.3233/JAD-2010-090649.

Abstract

In this study we investigated the cerebrospinal fluid (CSF) levels of neurofilament light (NFL) and heavy chain (NFHp35), total tau (t-tau), and glial fibrillary acidic protein (GFAP) to detect disease specific profiles in sporadic Creutzfeldt Jakob disease (sCJD) patients and Alzheimer's disease (AD) patients. CSF levels of NFL, NFHp35, t-tau, and GFAP of 23 sCJD patients and 55 AD patients were analyzed and compared to non-demented controls. Median NFL, NFHp35, GFAP, and t-tau levels were significantly increased in sCJD patients and AD patients versus controls (p < 0.0001 in all). NFL, NFHp35, and t-tau levels were significantly increased in sCJD patients versus AD patients (p < 0.005), but GFAP concentrations did not differ between sCJD and AD. The results suggest that neuroaxonal damage, reflected by higher CSF levels of NFL, NFHp35, and t-tau, is more pronounced in the pathophysiology of sCJD than in AD. The comparable CSF GFAP concentrations suggest that astroglial damage or astrocytosis is equally pronounced in the pathophysiology of AD and sCJD. Prospective studies are needed to determine whether NFL and NFHp35 may be additional tools in the differential diagnosis of rapidly progressive dementias.

摘要

在这项研究中,我们调查了神经丝轻链(NFL)和重链(NFHp35)、总tau(t-tau)和胶质纤维酸性蛋白(GFAP)在散发型克雅氏病(sCJD)患者和阿尔茨海默病(AD)患者中的脑脊液(CSF)水平,以检测疾病特异性谱。分析了 23 例 sCJD 患者和 55 例 AD 患者的 CSF NFL、NFHp35、t-tau 和 GFAP 水平,并与非痴呆对照组进行比较。sCJD 患者和 AD 患者的 CSF NFL、NFHp35、GFAP 和 t-tau 水平中位数明显高于对照组(p<0.0001)。sCJD 患者的 NFL、NFHp35 和 t-tau 水平明显高于 AD 患者(p<0.005),但 sCJD 和 AD 之间 GFAP 浓度无差异。结果表明,神经轴突损伤,反映在 CSF 中更高的 NFL、NFHp35 和 t-tau 水平,在 sCJD 的病理生理学中比在 AD 中更为明显。相当的 CSF GFAP 浓度表明,星形胶质细胞损伤或星形胶质细胞增生在 AD 和 sCJD 的病理生理学中同样明显。需要前瞻性研究来确定 NFL 和 NFHp35 是否可能是快速进行性痴呆鉴别诊断的附加工具。

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