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Parkinson's disease (PD) and dementia with Lewy bodies (DLB) are neurodegenerative diseases characterized by the pathological accumulation of α-synuclein in cells, called Lewy bodies
In contrast to PD and DLB, the neuropathological feature of progressive supranuclear palsy (PSP) is the intracellular accumulation of the microtubule-associated protein tau
diagnosis
So far, the diagnostic biomarkers for PD include structural and functional imaging, as well as the analysis of cerebrospinal fluid (CSF) alpha-synuclein at an experimental level, which is reduced in PD
Less invasive biomarkers are preferable to CSF markers.
Biomarkers should best reflect the main aspects of the basic pathology of the disease
One possible way is the transfer of α-synuclein with extracellular vesicles (EVs)
Alpha-synuclein is released together with EVs in vitro and in vivo
In this way, Anne Stuendl and others of the University of Bonn in Germany explored the diagnostic potential of plasma EV-related α-synuclein for PD and DLB (another α-synuclein-related neurodegenerative disease), PSP (a non- Differential diagnosis of α-synuclein-related atypical Parkinson's disease), healthy controls (HCs) and nervous system controls (NCs)
Anne Stuendl of the University of Bonn, Germany, discussed the diagnostic potential of plasma EV-related α-synuclein, and Anne Stuendl of the University of Bonn, Germany, discussed the diagnostic potential of plasma EV-related α-synuclein
They first established an optimized detection method for preparing plasma extracellular capsules and detecting α-synuclein derived from extracellular capsules
They found that the concentration of α-synaptic nucleotides in plasma extracellular vesicles had the best distinction between PD, Lewy body dementia, PSP and healthy controls
Specifically, in the Tubingen cohort, the area under the curve was 0.
In the Tubingen cohort, the area under the curve was 0.
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