| Literature DB >> 26411482 |
Markus Waser1, Heinrich Garn2, Reinhold Schmidt3, Thomas Benke4, Peter Dal-Bianco5, Gerhard Ransmayr6, Helena Schmidt7, Stephan Seiler3, Günter Sanin4, Florian Mayer5, Georg Caravias6, Dieter Grossegger8, Wolfgang Frühwirt8, Manfred Deistler9.
Abstract
We analyzed the relation of several synchrony markers in the electroencephalogram (EEG) and Alzheimer's disease (AD) severity as measured by Mini-Mental State Examination (MMSE) scores. The study sample consisted of 79 subjects diagnosed with probable AD. All subjects were participants in the PRODEM-Austria study. Following a homogeneous protocol, the EEG was recorded both in resting state and during a cognitive task. We employed quadratic least squares regression to describe the relation between MMSE and the EEG markers. Factor analysis was used for estimating a potentially lower number of unobserved synchrony factors. These common factors were then related to MMSE scores as well. Most markers displayed an initial increase of EEG synchrony with MMSE scores from 26 to 21 or 20, and a decrease below. This effect was most prominent during the cognitive task and may be owed to cerebral compensatory mechanisms. Factor analysis provided interesting insights in the synchrony structures and the first common factors were related to MMSE scores with coefficients of determination up to 0.433. We conclude that several of the proposed EEG markers are related to AD severity for the overall sample with a wide dispersion for individual subjects. Part of these fluctuations may be owed to fluctuations and day-to-day variability associated with MMSE measurements. Our study provides a systematic analysis of EEG synchrony based on a large and homogeneous sample. The results indicate that the individual markers capture different aspects of EEG synchrony and may reflect cerebral compensatory mechanisms in the early stages of AD.Entities:
Keywords: Alzheimer’s disease; Canonical correlation; Coherence; Compensatory mechanism; EEG synchrony markers; Granger causality
Mesh:
Year: 2015 PMID: 26411482 PMCID: PMC4766239 DOI: 10.1007/s00702-015-1461-x
Source DB: PubMed Journal: J Neural Transm (Vienna) ISSN: 0300-9564 Impact factor: 3.575