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Elecsys® Total-Tau and Phospho-Tau (181P) CSF assays: Analytical performance of the novel, fully automated immunoassays for quantification of tau proteins in human cerebrospinal fluid

  • Valeria Lifke*
  • , Gwendlyn Kollmorgen
  • , Ekaterina Manuilova
  • , Tobias Oelschlaegel
  • , Lars Hillringhaus
  • , Monika Widmann
  • , Christine A. F. von Arnim
  • , Markus Otto
  • , Robert H. Christenson
  • , Jennifer L. Powers
  • , Leslie M. Shaw
  • , Oskar Hansson
  • , James D. Doecke
  • , Qiao-Xin Li
  • , Charlotte Teunissen
  • , Hayrettin Tumani
  • , Kaj Blennow
  • *Corresponding author for this work
  • Roche Diagnostics GmbH
  • Amsterdam UMC location University of Amsterdam
  • Ulm University
  • University of Maryland, Baltimore
  • Washington University St. Louis
  • University of Pennsylvania
  • Lund University
  • CSIRO
  • University of Melbourne
  • Amsterdam UMC - Vrije Universiteit Amsterdam
  • Sahlgrenska University Hospital
  • University of Gothenburg
  • Roche Diagnostics GmbH, 82377 Penzberg, Germany
  • Amsterdam University Medical Center, 1081 Amsterdam, Germany
  • Clinic for Neurology, 89081 Ulm, Germany
  • Department of Pathology, 21201 Baltimore, United States
  • Division of Endocrinology, 63110 St. Louis, United States
  • Department of Pathology and Laboratory Medicine, 19104 Philadelphia, United States
  • Clinical Memory Research Unit, 212 24 Malmö, Sweden
  • Memory Clinic, 214 21 Malmö, Sweden
  • The Commonwealth Scientific and Industrial Research Organisation/Australian E-Health Research Centre, 4029 Herston, Australia
  • The Florey Institute of Neuroscience and Mental Health, 3052 Parkville, Australia
  • Neurochemistry Laboratory and Biobank, 1081 Amsterdam, Netherlands
  • Clinical Neurochemistry Laboratory, 431 80 Mölndal, Sweden
  • Institute of Neuroscience and Physiology, 431 41 Mölndal, Sweden

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

Background: Total tau (tTau) and phosphorylated 181P tau (pTau) are supportive diagnostic cerebrospinal fluid (CSF) biomarkers for Alzheimer's disease. Manual CSF tau assays are limited by lot-to-lot and between-laboratory variability and long incubation/turnaround times. Elecsys® Total-Tau CSF and Phospho-Tau (181P) CSF immunoassays were developed for fully automated cobas e analyzers, allowing broader access in clinical practice and trials. Methods: Analytical performance, reproducibility, method comparisons with commercially available assays, and lot-to-lot and platform comparability (cobas e 601/411) of the Elecsys® CSF assays were assessed. Tau distributions and concentration ranges were evaluated in CSF samples from two clinical cohorts. Results: Both assays showed high sensitivity (limit of quantitation [LoQ]: 63 pg/mL [tTau]; 4 pg/mL [pTau]) and linearity over the measuring range (80–1300 pg/mL; 8–120 pg/mL), which covered the entire concentration range measured in clinical samples. Lot-to-lot and platform comparability demonstrated good consistency (Pearson's r: 0.998; 1.000). Multicenter evaluation coefficients of variation (CVs): repeatability, < 1.8%; intermediate precision, < 2.8%; between-laboratory variability, < 2.7% (both assays); and total reproducibility, < 6.7% (tTau) and < 4.7% (pTau). Elecsys® CSF assays demonstrated good correlation with commercially available tau assays. Conclusions: Elecsys® Total-Tau CSF and Phospho-Tau (181P) CSF assays demonstrate good analytical performance with clinically relevant measuring ranges; data support their use in clinical trials and practice.
Original languageEnglish
Pages (from-to)30-38
JournalClinical biochemistry
Volume72
DOIs
Publication statusPublished - 1 Oct 2019

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