- February 6, 2026
- Thomas K. Karikari, University of Pittsburgh
Topic/Product:
Alzheimer's, CNS Disease Panel 120, pTau217
Disease Area:
Alzheimer's Disease
Sample Type:
Plasma
Abstract
Abstract
Background
Plasma p-tau217 is a promising biomarker for detecting incipient AD pathology, but direct comparison of different p-tau217 assays in community-based cohorts are limited.
Methods
We evaluated two cohorts from southwestern Pennsylvania, USA; the MYHAT-NI study, which included two-year longitudinal follow-up neuroimaging assessments of Aβ, tau, and cortical thickness; and the Human Connectome Project/CoBRA cohort, targeting a 50:50 split of self-identified Black and non-Hispanic White individuals. Plasma p-tau217 was measured using four different assays: Lumipulse, Johnson & Johnson, ALZpath, and NULISA. Aβ and tau pathologies were assessed with [11C]PiB PET and [18F]Flortaucipir PET, respectively. Clinical Dementia Rating and Montreal Cognitive Assessment were used to assess cognitive performance.
Results
We included 344 participants (MYHAT-NI: n = 111, median age 76 [IQR: 72–80], 54% female; HCP/CoBRA: n = 234, median age 62 [IQR: 52–70], 65% female). All four p-tau217 assays exhibited moderate to strong cross-platform correlations (Spearman correlations of 0.40–0.86), and statistically equivalent AUCs (of 0.84–0.90) for determining Aβ positivity.
Conclusions
Our findings show strong equivalent performances of plasma p-tau217 assays to identify amyloid positivity across two highly diverse cohorts of community-dwelling older adults.
Authors & Affiliations
Rebecca A. Deek1,3†, Wasiu G. Balogun2,3,4†, Xuemei Zeng2,3,4, Gallen Triana-Baltzer5, Tharick A. Pascoal2,3,6,
Hartmuth C. Kolb5, Beth Snitz3,6, Ann D. Cohen2,3 and Thomas K. Karikari2,3,4*
†Rebecca A. Deek and Wasiu G. Balogun contributed equally to this
work.
*Correspondence:
Thomas K. Karikari
Karikaritk@upmc.edu
1Department of Biostatistics and Health Data Science, School of Public
Health, University of Pittsburgh, Pittsburgh, Pennsylvania, USA
2Department of Psychiatry, School of Medicine, University of Pittsburgh,
Pittsburgh, Pennsylvania, USA
3Alzheimer’s Disease Research Center, University of Pittsburgh, Pittsburgh,
PA, USA
4Biofluid Biomarker Laboratory, Western Psychiatric Hospital, University of
Pittsburgh Medical Center, Pittsburgh, PA, USA
5Johnson & Johnson, La Jolla, California, USA
6Department of Neurology, School of Medicine, University of Pittsburgh,
Pittsburgh, Pennsylvania, USA