| Literature DB >> 26550994 |
Istvan Horvath1, Xueen Jia1,2, Per Johansson3,4, Chao Wang1, Roman Moskalenko1,5, Andreas Steinau1, Lars Forsgren6, Thomas Wågberg2, Johan Svensson4,7, Henrik Zetterberg8,9, Ludmilla A Morozova-Roche1.
Abstract
Pro-inflammatory protein S100A9 was established as a biomarker of dementia progression and compared with others such as Aβ(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 Aβ(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 Aβ(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.Entities:
Keywords: Alzheimer’s disease; Aβ1−42; S100A9; amyloid; biomarkers; cerebrospinal fluid; inflammation; mild cognitive impairment
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Year: 2015 PMID: 26550994 DOI: 10.1021/acschemneuro.5b00265
Source DB: PubMed Journal: ACS Chem Neurosci ISSN: 1948-7193 Impact factor: 4.418