| Literature DB >> 30421149 |
Hannah Pellkofer1, Friedrich Ihler2, Bernhard G Weiss2, Janina Trothe3,4, Harindranath Kadavath3, Monika Chongtham3, Marcel Kunadt5, Dietmar Riedel6, Finn Lornsen5, Petra Wilken5, Claudia Bartels5, Sina Hirschel5, Sebastian G Russo6, Elke Stransky7, Lutz Trojan8, Boris Schmidt9, Eckhardt Mandelkow10,11,12, Markus Zweckstetter1,3,4, Martin Canis2, Anja Schneider13,14.
Abstract
Alzheimer's disease (AD) pathology precedes the onset of clinical symptoms by several decades. Thus, biomarkers are required to identify prodromal disease stages to allow for the early and effective treatment. The methoxy-X04-derivative BSC4090 is a fluorescent ligand which was designed to target neurofibrillary tangles in AD. BSC4090 staining was previously detected in post-mortem brains and olfactory mucosa derived from AD patients. We tested BSC4090 as a potential diagnostic marker of prodromal and early AD using olfactory mucosa biopsies from 12 individuals with AD, 13 with mild cognitive impairment (MCI), and 10 cognitively normal (CN) controls. Receiver-operating curve analysis revealed areas under the curve of 0.78 for AD versus CN and of 0.86 for MCI due to AD versus MCI of other causes. BSC4090 labeling correlated significantly with cerebrospinal fluid levels of tau protein phosphorylated at T181. Using NMR spectroscopy, we find that BSC4090 binds to fibrillar and pre-fibrillar but not to monomeric tau. Thus, BSC4090 may be an interesting candidate to detect AD at the early disease stages.Entities:
Keywords: Alzheimer’s disease; Biomarker; Methoxy-X04; Olfactory epithelia; Tau
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Year: 2018 PMID: 30421149 DOI: 10.1007/s00406-018-0955-6
Source DB: PubMed Journal: Eur Arch Psychiatry Clin Neurosci ISSN: 0940-1334 Impact factor: 5.270