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Crosswalk study on blood collection-tube types for Alzheimer's disease biomarkers.

Authors :
Jonaitis EM
Zetterberg H
Koscik RL
Betthauser TJ
Van Hulle CA
Hogan K
Hegge L
Kollmorgen G
Suridjan I
Gleason CE
Engelman CD
Okonkwo OC
Asthana S
Bendlin BB
Carlsson CM
Johnson SC
Blennow K
Source :
Alzheimer's & dementia (Amsterdam, Netherlands) [Alzheimers Dement (Amst)] 2022 Feb 09; Vol. 14 (1), pp. e12266. Date of Electronic Publication: 2022 Feb 09 (Print Publication: 2022).
Publication Year :
2022

Abstract

Introduction: Blood-based Alzheimer's disease (AD) biomarkers show promise, but pre-analytical protocol differences may pose problems. We examined seven AD blood biomarkers (amyloid beta [ A β ] 42 , A β 40 , phosphorylated tau [ p - ta u 181 , total tau [t-tau], neurofilament light chain [NfL], A β 42 40 , and p - ta u 181 A β 42 ) in three collection tube types (ethylenediaminetetraacetic acid [EDTA] plasma, heparin plasma, serum).<br />Methods: Plasma and serum were obtained from cerebrospinal fluid or amyloid positron emission tomography-positive and -negative participants (N = 38) in the Wisconsin Registry for Alzheimer's Prevention. We modeled AD biomarker values observed in EDTA plasma versus heparin plasma and serum, and assessed correspondence with brain amyloidosis.<br />Results: Results suggested bias due to tube type, but crosswalks are possible for some analytes, with excellent model fit for NfL ( R 2 = 0.94), adequate for amyloid ( R 2 = 0.40-0.69), and weaker for t-tau ( R 2 = 0.04-0.42) and p - ta u 181 ( R 2 = 0.22-0.29). Brain amyloidosis differentiated several measures, especially EDTA plasma pTa u 181 A β 42 ( d = 1.29).<br />Discussion: AD biomarker concentrations vary by tube type. However, correlations for some biomarkers support harmonization across types, suggesting cautious optimism for use in banked blood.<br />Competing Interests: SCJ serves on an advisory board for Roche Diagnostics. KB has served as a consultant, on advisory boards, or on data monitoring committees for Abcam, Axon, Biogen, JOMDD/Shimadzu, Julius Clinical, Lilly, MagQu, Novartis, Roche Diagnostics, and Siemens Healthineers, and is a co‐founder of Brain Biomarker Solutions in Gothenburg AB (BBS), which is a part of the GU Ventures Incubator Program, all unrelated to the present study. HZ has served on scientific advisory boards for Eisai, Denali, Roche Diagnostics, Wave, Samumed, Siemens Healthineers, Pinteon Therapeutics, Nervgen, AZTherapies, and CogRx; has given lectures in symposia sponsored by Cellectricon, Fujirebio, Alzecure, and Biogen; and is a co‐founder of Brain Biomarker Solutions in Gothenburg AB (BBS), which is a part of the GU Ventures Incubator Program (outside submitted work). BB has received precursors and tracers from Avid Radiopharmaceuticals. CEG is a member of the Executive Board for the Alzheimer's and Dementia Alliance of Wisconsin, and receives support from the Alzheimer's Association for travel to AAIC, for which she is on the Scientific Program Committee. GK is a full‐time employee of Roche Diagnostics GmbH. IS is a full‐time employee and shareholder of Roche Diagnostics International Ltd. Authors KH, CE, OO, TB, CVH, RK, LH, and EMJ have no disclosures.<br /> (© 2021 The Authors. Alzheimer's & Dementia: Diagnosis, Assessment & Disease Monitoring published by Wiley Periodicals, LLC on behalf of Alzheimer's Association.)

Details

Language :
English
ISSN :
2352-8729
Volume :
14
Issue :
1
Database :
MEDLINE
Journal :
Alzheimer's & dementia (Amsterdam, Netherlands)
Publication Type :
Academic Journal
Accession number :
35155728
Full Text :
https://doi.org/10.1002/dad2.12266