Blood plasma phosphorylated-tau isoforms track CNS change in Alzheimer's disease

Research output: Contribution to journalArticlepeer-review

5 Scopus citations

Abstract

Highly sensitive and specific plasma biomarkers for Alzheimer's disease (AD) have the potential to improve diagnostic accuracy in the clinic and facilitate research studies including enrollment in prevention and treatment trials. We recently reported CSF tau hyperphosphorylation, especially on T217, is an accurate predictor of β-amyloidosis at asymptomatic and symptomatic stages. In the current study, we determine by mass spectrometry the potential utility of plasma p-tau isoforms to detect AD pathology and investigate CSF and plasma tau isoforms' profile relationships. Plasma tau was truncated as previously described in CSF. CSF and plasma measures of p-tau-217 and p-tau-181 were correlated. No correlation was found between CSF and plasma on total-tau levels and pS202 measures. We found p-tau-217 and p-tau-181 were highly specific for amyloid plaque pathology in the discovery cohort (n = 36, AUROC = 0.99 and 0.98 respectively). In the validation cohort (n = 92), p-tau-217 measures were still specific to amyloid status (AUROC = 0.92), and p-tau-181 measures were less specific (AUROC = 0.75).

Original languageEnglish
Article number20200861
JournalJournal of Experimental Medicine
Volume217
Issue number11
DOIs
StatePublished - Jul 2020

Fingerprint Dive into the research topics of 'Blood plasma phosphorylated-tau isoforms track CNS change in Alzheimer's disease'. Together they form a unique fingerprint.

Cite this