Isolation of neuronal exosomes from blood allows for prediction of individuals who are likely to progress to PD, and differentiate those with PD from Parkinson’s-like diseases. Suitable for clinical trial recruitment.
Features
Benefits
Identification of the neuronal exosomes that contain clinically relevant information
Targeted exosome analysis removes confusion seen in many studies of α-synuclein as a biomarker
Two biomarkers that can be measured associated with PD – α-synuclein and Clusterin
Greater than 90% sensitivity and specificity in differentiation of PD, even in the prodromal phase
Biomarkers validated on large international cohorts
Strong evidence supporting the use of these biomarkers amongst three PD cohorts
Differentiate healthy controls from individuals with PD or will develop PD, and those with PD-like disease, tauopathies, non-α-synuclein proteinopathies
Diagnostic applications
Predictive applications
Screening applications
Suitable for clinical trial recruitment
Run using blood-based samples – whole blood, serum, plasma
Allows for rapid high throughput analysis and patient screening