Equivalence of plasma p‐tau217 with cerebrospinal fluid in the diagnosis of Alzheimer's disease

• Published in: Alzheimer's & dementia Vol. 19; no. 11; pp. 4967 - 4977
• Main Authors: Therriault, Joseph, Servaes, Stijn, Tissot, Cécile, Rahmouni, Nesrine, Ashton, Nicholas J., Benedet, Andréa Lessa, Karikari, Thomas K., Macedo, Arthur C., Lussier, Firoza Z., Stevenson, Jenna, Wang, Yi‐Ting, Fernandez‐Arias, Jaime, Stevenson, Alyssa, Socualaya, Kely Quispialaya, Haeger, Arlette, Nazneen, Tahnia, Aumont, Étienne, Hosseini, Ali, Rej, Soham, Vitali, Paolo, Triana‐Baltzer, Gallen, Kolb, Hartmuth C., Soucy, Jean‐Paul, Pascoal, Tharick A., Gauthier, Serge, Zetterberg, Henrik, Blennow, Kaj, Rosa‐Neto, Pedro
• Format: Journal Article
• Language: English
• Published: United States 01.11.2023
• Subjects: Alzheimer Disease - diagnosis; Alzheimer's disease; Amyloid beta-Peptides; amyloid-beta; Amyloidogenic Proteins; Biomarkers; CSF; Humans; Neurosciences; Neurovetenskaper; p-tau; PET; Plasma; Spinal Puncture; tau; tau Proteins; CSF; amyloid-β; tau; p-tau; plasma; Alzheimer's disease; PET
• ISSN: 1552-5260; 1552-5279; 1552-5279
• DOI: 10.1002/alz.13026

Plasma biomarkers are promising tools for Alzheimer's disease (AD) diagnosis, but comparisons with more established biomarkers are needed. We assessed the diagnostic performance of p-tau , p-tau , and p-tau in plasma and CSF in 174 individuals evaluated by dementia specialists and assessed with amyloid-PET and tau-PET. Receiver operating characteristic (ROC) analyses assessed the performance of plasma and CSF biomarkers to identify amyloid-PET and tau-PET positivity. Plasma p-tau biomarkers had lower dynamic ranges and effect sizes compared to CSF p-tau. Plasma p-tau (AUC = 76%) and p-tau (AUC = 82%) assessments performed inferior to CSF p-tau (AUC = 87%) and p-tau (AUC = 95%) for amyloid-PET positivity. However, plasma p-tau (AUC = 91%) had diagnostic performance indistinguishable from CSF (AUC = 94%) for amyloid-PET positivity. Plasma and CSF p-tau had equivalent diagnostic performance for biomarker-defined AD. Our results suggest that plasma p-tau may help reduce the need for invasive lumbar punctures without compromising accuracy in the identification of AD. p-tau in plasma performed equivalent to p-tau in CSF for the diagnosis of AD, suggesting the increased accessibility of plasma p-tau is not offset by lower accuracy. p-tau biomarkers in plasma had lower mean fold-changes between amyloid-PET negative and positive groups than p-tau biomarkers in CSF. CSF p-tau biomarkers had greater effect sizes than plasma p-tau biomarkers when differentiating between amyloid-PET positive and negative groups. Plasma p-tau and plasma p-tau performed worse than p-tau and p-tau in CSF for AD diagnosis.