Cortical phosphorylated α-Synuclein levels correlate with brain wave spectra in Parkinson's disease.

Autor: Caviness JN; Department of Neurology, Mayo Clinic, Scottsdale, Arizona, USA., Lue LF; Laboratories of Neuroregeneration and Neuroinflammation, Banner-Sun Health Research Institute, Sun City, Arizona, USA., Hentz JG; Department of Biostatistics, Mayo Clinic, Scottsdale, Arizona, USA., Schmitz CT; Laboratories of Neuroregeneration and Neuroinflammation, Banner-Sun Health Research Institute, Sun City, Arizona, USA., Adler CH; Department of Neurology, Mayo Clinic, Scottsdale, Arizona, USA., Shill HA; Cleo Roberts Center, Banner-Sun Health Research Institute, Sun City, Arizona, USA., Sabbagh MN; Cleo Roberts Center, Banner-Sun Health Research Institute, Sun City, Arizona, USA., Beach TG; Department of Neuropathology, Banner-Sun Health Research Institute, Sun City, Arizona, USA., Walker DG; Laboratories of Neuroregeneration and Neuroinflammation, Banner-Sun Health Research Institute, Sun City, Arizona, USA.
Jazyk: angličtina
Zdroj: Movement disorders : official journal of the Movement Disorder Society [Mov Disord] 2016 Jul; Vol. 31 (7), pp. 1012-9. Date of Electronic Publication: 2016 Apr 08.
DOI: 10.1002/mds.26621
Abstrakt: Introduction: Quantitative EEG features have been identified as surrogates and predictors of cognitive decline/dementia, a common feature of progressive PD. The biochemical correlates for altered quantitative EEG features are unknown. Our primary objective was to test the hypothesis that quantitative EEG measures correlate with cortical levels of phosphorylated α-synuclein, a modified form of the synaptic protein α-synuclein, in PD cases, in contrast to other pathology-associated proteins. A secondary objective was to explore the same correlations among cellular fractions of these proteins.
Methods: We used posterior cingulate cortex autopsy tissue from 44 PD subjects with various degrees of cognitive decline, who had undergone EEG. In this brain region, which is a major hub of the default mode network, biochemical measurements for levels of phosphorylated α-synuclein, unmodified α-synuclein, amyloid beta peptide, phosphorylated tau, and key synaptic proteins were analyzed and data correlated with spectral EEG measures.
Results: Findings revealed significant correlations between background rhythm peak frequency and all bandpower values (highest in delta bandpower) with total phosphorylated α-synuclein, but not any correlation with total α-synuclein, phosphorylated tau protein, amyloid beta peptide, or synaptic proteins. Certain fractions of synaptosomal-associated protein 25 showed correlation with some quantitative EEG measures.
Conclusions: These data show an association between increased phosphorylation of α-synuclein and the abnormal EEG signatures of cognitive decline. Results suggest that quantitative EEG may provide an in vivo approximation of phosphorylated α-synuclein in PD cortex. This adds to previous evidence that quantitative EEG measures can be considered valid biomarkers of PD cognitive decline. © 2016 International Parkinson and Movement Disorder Society.
(© 2016 International Parkinson and Movement Disorder Society.)
Databáze: MEDLINE