Equivalence of plasma p‐tau217 with cerebrospinal fluid in the diagnosis of Alzheimer's disease
Joseph Therriault, Stijn Servaes, Cécile Tissot, Nesrine Rahmouni, Nicholas J. Ashton, Andréa Lessa Benedet, Thomas K. Karikari, Arthur C. Macedo, Firoza Z Lussier, Jenna Stevenson, Yi‐Ting Wang, Jaime Fernandez‐Arias, Alyssa Stevenson, Kely Quispialaya Socualaya, Arlette Haeger, Tahnia Nazneen, Étienne Aumont, Seyyed Ali Hosseini, Soham Rej, Paolo Vitali, Gallen Triana‐Baltzer, Hartmuth C. Kolb, Jean‐Paul Soucy, Tharick A. Pascoal, Serge Gauthier, Henrik Zetterberg, Kaj Blennow, Pedro Rosa‐Neto
Abstract
Abstract INTRODUCTION Plasma biomarkers are promising tools for Alzheimer's disease (AD) diagnosis, but comparisons with more established biomarkers are needed. METHODS We assessed the diagnostic performance of p‐tau 181 , p‐tau 217 , and p‐tau 231 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. RESULTS Plasma p‐tau biomarkers had lower dynamic ranges and effect sizes compared to CSF p‐tau. Plasma p‐tau 181 (AUC = 76%) and p‐tau 231 (AUC = 82%) assessments performed inferior to CSF p‐tau 181 (AUC = 87%) and p‐tau 231 (AUC = 95%) for amyloid‐PET positivity. However, plasma p‐tau 217 (AUC = 91%) had diagnostic performance indistinguishable from CSF (AUC = 94%) for amyloid‐PET positivity. DISCUSSION Plasma and CSF p‐tau 217 had equivalent diagnostic performance for biomarker‐defined AD. Our results suggest that plasma p‐tau 217 may help reduce the need for invasive lumbar punctures without compromising accuracy in the identification of AD. Highlights p‐tau 217 in plasma performed equivalent to p‐tau 217 in CSF for the diagnosis of AD, suggesting the increased accessibility of plasma p‐tau 217 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 181 and plasma p‐tau 231 performed worse than p‐tau 181 and p‐tau 231 in CSF for AD diagnosis.