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Updated: Nov 28, 2025

A High Throughput, Multiplexed and Targeted Proteomic CSF Assay to Quantify Neurodegenerative Biomarkers and Apolipoprotein E Isoforms Status
Published on: October 20, 2016
Cerebrospinal fluid biomarker profiling in corticobasal degeneration: Application of the AT(N) and other
Vasilios C Constantinides1, George P Paraskevas2, Fotini Boufidou3
1Department of Neurology, National and Kapodistrian University of Athens, School of Medicine, Eginition Hospital, Neurochemistry and Biomarkers Unit, Greece; Department of Neurology, National and Kapodistrian University of Athens, School of Medicine, Eginition Hospital, Division of Cognitive, Movement Disorders and Epilepsy, Greece.
Introduction:
Total tau (τT), phosphorylated tau (τP-181) and amyloid beta (Aβ42) are cerebrospinal fluid (CSF) biomarkers of Alzheimer's disease (AD). There is no consensus on the interpretation criteria of these biomarkers. The aim of this study was to apply three different sets of criteria for CSF AD biomarker interpretation in a cohort of corticobasal degeneration (CBD) patients.
Method:
SForty patients fulfilling diagnostic criteria for "probable CBD" were included. The AT(N), BIOMARKAPD/ABSI and the τP-181/Aβ42 ratio criteria were applied.
Results:
The AT(N) criteria categorized 50% of "probable CBD" patients as AD, and 62.5% as harboring amyloid pathology. The BIOMARKAPD/ABSI and τP- 181/Aβ42 criteria categorized ~40% of "probable CBD" patients as AD.
Discussion:
Use of different interpretation criteria for CSF AD biomarkers produces diverse results. AD pathology is common in patients fulfilling "probable" CBD criteria. CBD diagnostic criteria may have suboptimal positive predictive value. A consensus regarding interpretation criteria of CSF AD biomarkers is pivotal.

