Ontology highlight
ABSTRACT: Objective
The high degree of clinical overlap between atypical parkinsonian syndromes (APS) and Parkinson's disease (PD) makes diagnosis challenging. We aimed to identify novel diagnostic protein biomarkers of APS using multiplex proximity extension assay (PEA) testing.Methods
Cerebrospinal fluid (CSF) samples from two independent cohorts, each consisting of APS and PD cases, and controls, were analysed for neurofilament light chain (NF-L) and Olink Neurology and Inflammation PEA biomarker panels. Whole-cohort comparisons of biomarker concentrations were made between APS (n=114), PD (n=37) and control (n=34) groups using logistic regression analyses that included gender, age and disease duration as covariates.Results
APS versus controls analyses revealed 11 CSF mark
SUBMITTER: Jabbari E
PROVIDER: S-EPMC6585258 | biostudies-literature | 2019 Jul
REPOSITORIES: biostudies-literature