Tau oligomers in cerebrospinal fluid in Alzheimer's disease

被引:61
作者
Sengupta, Urmi [1 ,2 ]
Portelius, Erik [3 ]
Hansson, Oskar [4 ,5 ]
Farmer, Kathleen [1 ,2 ]
Castillo-Carranza, Diana [1 ,2 ]
Woltjer, Randall [7 ]
Zetterberg, Henrik [3 ,6 ]
Galasko, Douglas [8 ]
Blennow, Kaj [3 ]
Kayed, Rakez [1 ,2 ]
机构
[1] Univ Texas Med Branch, Mitchell Ctr Neurodegenerat Dis, 301 Univ Blvd,Med Res Bldg, Galveston, TX 77555 USA
[2] Univ Texas Med Branch, Dept Neurol & Neurosci & Cell Biol, 301 Univ Blvd,Med Res Bldg, Galveston, TX 77555 USA
[3] Univ Gothenburg, Sahlgrenska Acad, Inst Neurosci & Physiol, Clin Neurochem Lab, Molndal, Sweden
[4] Lund Univ, Dept Clin Sci, Clin Memory Res Unit, Lund, Sweden
[5] Skane Univ Hosp, Memory Clin, Lund, Sweden
[6] UCL Inst Neurol, Dept Mol Neurosci, Queen Sq, London WC1N 3BG, England
[7] Oregon Hlth & Sci Univ, Dept Dept Pathol, Portland, OR 97201 USA
[8] Univ Calif San Diego, Dept Neurosci, San Diego, CA USA
关键词
MILD COGNITIVE IMPAIRMENT; PHOSPHORYLATED TAU; CLINICAL-DIAGNOSIS; BIOMARKERS; CSF; PREDICTION; PROTEIN; A-BETA-42; DEMENTIA; SPECTRUM;
D O I
10.1002/acn3.382
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: With an increasing incidence of Alzheimer's disease (AD) and neurodegenerative tauopathies, there is an urgent need to develop reliable biomarkers for the diagnosis and monitoring of the disease, such as the recently discovered toxic tau oligomers. Here, we aimed to demonstrate the presence of tau oligomers in the cerebrospinal fluid (CSF) of patients with cognitive deficits, and to determine whether tau oligomers could serve as a potential biomarker for AD. Methods: A multicentric collaborative study involving a double-blinded analysis with a total of 98 subjects with moderate to severe AD (N = 41), mild AD (N = 31), and nondemented control subjects (N = 26), and two pilot studies of 33 total patients with AD (N = 19) and control (N = 14) subjects were performed. We carried out biochemical assays to measure oligomeric tau from CSF of these patients with various degrees of cognitive impairment as well as cognitively normal controls. Results: Using a highly reproducible indirect ELISA method, we found elevated levels of tau oligomers in AD patients compared to age-matched controls. Western blot analysis confirmed the presence of oligomeric forms of tau in CSF. In addition, the ratio of oligomeric to total tau increased in the order: moderate to severe AD, mild AD, and controls. Conclusion: These assays are suitable for the analysis of human CSF samples. These results here suggest that CSF tau oligomer measurements could be optimized and added to the panel of CSF biomarkers for the accurate and early detection of AD.
引用
收藏
页码:226 / 235
页数:10
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