| Literature DB >> 24373987 |
Michael Deuschle1, Claudia Schilling2, F Markus Leweke2, Frank Enning2, Thomas Pollmächer3, Hermann Esselmann4, Jens Wiltfang5, Lutz Frölich2, Isabella Heuser6.
Abstract
It has been suggested that sleep-wake regulation as well as hypocretins play a role in the pathophysiology of Alzheimer's disease. We analyzed Aβ40, Aβ42, Tau protein, phosphorylated Tau (pTau) protein as well as hypocretin-1 concentrations in the CSF of a detection sample of 10 patients with Alzheimer's disease (AD) as well as 10 age- and gender-matched patients with major depression as a comparison group of different pathology. In order to replicate the findings, we used a confirmation sample of 17 AD patients and 8 patients with major depression. We found hypocretin-1 concentrations in CSF not to differ between patients with depression and AD. However, hypocretin-1 was significantly related to Tau (r=0.463, p<0.001) and pTau (r=0.630, p<0.0001). These effects were more pronounced in depressed patients when compared to AD patients. We conclude that hypocretin-1 may play a role in the metabolism of Tau proteins across different diagnostic entities including AD. It has to be determined whether there is a causal relationship between hypocretin-1 and Tau as well as pTau.Entities:
Keywords: Alzheimer's disease; Aβ; Depression; Hypocretin; Orexin; Tau protein
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Year: 2013 PMID: 24373987 DOI: 10.1016/j.neulet.2013.12.036
Source DB: PubMed Journal: Neurosci Lett ISSN: 0304-3940 Impact factor: 3.046