Pro-inflammatory S100A9 Protein as a Robust Biomarker Differentiating Early Stages of Cognitive Impairment in Alzheimer's Disease

被引:63
作者
Horvath, Istvan [1 ]
Jia, Xueen [1 ,2 ]
Johansson, Per [3 ,4 ]
Wang, Chao [1 ]
Moskalenko, Roman [1 ,5 ]
Steinau, Andreas [1 ]
Forsgren, Lars [6 ]
Wagberg, Thomas [2 ]
Svensson, Johan [4 ,7 ]
Zetterberg, Henrik [8 ,9 ]
Morozova-Roche, Ludmilla A. [1 ]
机构
[1] Umea Univ, Dept Med Biochem & Biophys, S-90187 Umea, Sweden
[2] Umea Univ, Dept Phys, S-90187 Umea, Sweden
[3] Skaraborg Cent Hosp, Dept Neuropsychiat, S-52185 Falkoping, Sweden
[4] Univ Gothenburg, Dept Internal Med, Sahlgrenska Acad, S-41345 Gothenburg, Sweden
[5] Sumy State Univ, Dept Pathol, UA-40000 Sumy, Ukraine
[6] Umea Univ, Dept Pharmacol & Clin Neurosci, S-90187 Umea, Sweden
[7] Skaraborg Cent Hosp, Dept Endocrinol, S-54185 Skovde, Sweden
[8] Univ Gothenburg, Sahlgrenska Acad, Inst Neurosci & Physiol, Clin Neurochem Lab, S-43180 Molndal, Sweden
[9] UCL, Inst Neurol, Queen Sq, London WC1E 6BT, England
基金
英国医学研究理事会;
关键词
Alzheimer's disease; mild cognitive impairment; cerebrospinal fluid; S100A9; A beta(1-42); biomarkers; amyloid; inflammation; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; CEREBROSPINAL-FLUID BIOMARKERS; AMYLOID-BETA; PATHOLOGY; CRITERIA; TAU;
D O I
10.1021/acschemneuro.5b00265
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Pro-inflammatory protein S100A9 was established as a biomarker of dementia progression and compared with others such as A beta(1-42) and tau-proteins. CSF samples from 104 stringently diagnosed individuals divided into five subgroups were analyzed, including nondemented controls, stable mild cognitive impairment (SMCI), mild cognitive impairment due to Alzheimer's disease (MCI-AD), Alzheimer's disease (AD), and vascular dementia (VaD) patients. ELISA, dot-blotting, and electrochemical impedance spectroscopy were used as research methods. The S100A9 and A beta(1-42). levels correlated with each other: their CSF content decreased already at the SMCI stage and declined further under MCI AD, AD, and VaD conditions. Immunohistochemical analysis also revealed involvement of both A beta(1-42) and S100A9 in the amyloid-neuroinflammatory cascade already during SMCI. Tau proteins were not yet altered in SMCI; however their contents increased during MCI-AD and AD, diagnosing later dementia stages. Thus, four biomarkers together, reflecting different underlying pathological causes, can accurately differentiate dementia progression and also distinguish AD from VaD.
引用
收藏
页码:34 / 39
页数:6
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