Stability of plasma pTau217/Aβ42 ratio with delayed blood processing.
4 affiliations
- 1University of Kansas Medical Center Department of Neurology Kansas City Kansas USA.
- 2University of Kansas Alzheimer's Disease Research Center Fairway Kansas USA.
- 3University of Kansas Health System Department of Pathology and Laboratory Medicine Kansas City Kansas USA.
- 4Friedman Brain Institute Ronald M. Loeb Center for Alzheimer's Disease Icahn School of Medicine at Mount Sinai New York New York USA.
Abstract
Introduction
Blood-based biomarkers may improve access to Alzheimer's disease diagnosis, but use may be limited in clinics without on-site processing capability. We evaluated the stability of the plasma phosphorylated tau 217 (pTau217)/amyloid beta 42 (Aβ42) ratio after delayed whole-blood processing.Methods
We compared blood processed within 2 h or held at 4°C for approximately 24 or 48 h before centrifugation and analysis using the Fujirebio Lumipulse G1200. Stability was assessed using ordinary least squares regression, error index, Bland-Altman analysis, and Deming regression.Results
Correlations with the 2-h condition were high at both 24 and 48 h (R = 0.998). Both delayed conditions met prespecified regression and error-index criteria. Mean absolute percent error was 5.6% at 24 h and 9.8% at 48 h. Deming regression showed no constant bias, although proportional bias was observed at 48 h. No bias was observed for individual analytes for up to 48 h.Discussion
The pTau217/Aβ42 ratio in refrigerated whole blood remained stable for 24 h, with possible utility up to 48 h, supporting more flexible specimen-transport workflows.
Related
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- Comparative analysis of plasma pTau217, NfL and eight modifiable risk scores for 11-year dementia prediction in the HUNT Study
BibTeX
@article{mayfield2026stability,
title = {{Stability of plasma pTau217/Aβ42 ratio with delayed blood processing.}},
author = {Hana Mayfield and Casey S John and Jenae Pennington and Riley E Kemna and Maggie Kroeger and Amitava Dasgupta and Jeffrey M Burns and Fanny M Elahi and Melody Nelson and Jill K Morris},
journal = {Alzheimer's \& dementia (Amsterdam, Netherlands)},
year = {2026},
month = oct,
doi = {10.1002/dad2.70517},
url = {https://europepmc.org/article/MED/42908786},
note = {CC BY-NC},
}
RIS
TY - JOUR
TI - Stability of plasma pTau217/Aβ42 ratio with delayed blood processing.
AU - Hana Mayfield
AU - Casey S John
AU - Jenae Pennington
AU - Riley E Kemna
AU - Maggie Kroeger
AU - Amitava Dasgupta
AU - Jeffrey M Burns
AU - Fanny M Elahi
AU - Melody Nelson
AU - Jill K Morris
PY - 2026
DA - 2026/10/20
JO - Alzheimer's & dementia (Amsterdam, Netherlands)
DO - 10.1002/dad2.70517
UR - https://europepmc.org/article/MED/42908786
AB - Introduction Blood-based biomarkers may improve access to Alzheimer's disease diagnosis, but use may be limited in clinics without on-site processing capability. We evaluated the stability of the plasma phosphorylated tau 217 (pTau217)/amyloid beta 42 (Aβ42) ratio after delayed whole-blood processing.Methods We compared blood processed within 2 h or held at 4°C for approximately 24 or 48 h before centrifugation and analysis using the Fujirebio Lumipulse G1200. Stability was assessed using ordinary least squares regression, error index, Bland-Altman analysis, and Deming regression.Results Correlations with the 2-h condition were high at both 24 and 48 h (R = 0.998). Both delayed conditions met prespecified regression and error-index criteria. Mean absolute percent error was 5.6% at 24 h and 9.8% at 48 h. Deming regression showed no constant bias, although proportional bias was observed at 48 h. No bias was observed for individual analytes for up to 48 h.Discussion The pTau217/Aβ42 ratio in refrigerated whole blood remained stable for 24 h, with possible utility up to 48 h, supporting more flexible specimen-transport workflows.
SN - 2352-8729
ER -