| Literature DB >> 35340050 |
Patrick Oeckl1,2, Olivia Wagemann3,4, Steffen Halbgebauer1, Sarah Anderl-Straub1, Georg Nuebling3,4, Catharina Prix3, Sandra V Loosli3, Elisabeth Wlasich3, Adrian Danek3, Petra Steinacker1, Albert C Ludolph1,2, Johannes Levin3,4,5, Markus Otto1,6.
Abstract
This exploratory case-control study investigates the synaptic marker beta-synuclein in serum and plasma pTau181 in adults with Down syndrome (DS) with (sDS, n = 14) and without (aDS, n = 47) clinical symptoms of Alzheimer disease (AD) as well as euploid controls (n = 23). Beta-synuclein was higher in aDS and more pronounced in sDS (p < 0.0001), whereas pTau181 was only higher in sDS (p < 0.0001). Both markers showed good discriminatory power (area under the curve > 0.90) to distinguish symptomatic from asymptomatic AD. The data indicate that synaptic alterations belong to the earliest AD-associated events in DS and highlight the value of serum beta-synuclein as a potential early marker of AD. ANN NEUROL 2022;92:6-10.Entities:
Mesh:
Substances:
Year: 2022 PMID: 35340050 DOI: 10.1002/ana.26360
Source DB: PubMed Journal: Ann Neurol ISSN: 0364-5134 Impact factor: 10.422