- February 6, 2026
- Thomas K. Karikari, University of Pittsburgh
Topic/Product:
CNS Disease Panel 120
Disease Area:
Alzheimer's Disease
Sample Type:
Plasma
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*
¹ Department of Biostatistics and Health Data Science, School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania, USA
² Department of Psychiatry, School of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania, USA
³ Alzheimer’s Disease Research Center, University of Pittsburgh, Pittsburgh, PA, USA
⁴ Biofluid Biomarker Laboratory, Western Psychiatric Hospital, University of Pittsburgh Medical Center, Pittsburgh, PA, USA
⁵ Johnson & Johnson, La Jolla, California, USA
⁶ Department of Neurology, School of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania, USA
† Rebecca A. Deek and Wasiu G. Balogun contributed equally to this work.
* Corresponding author: Thomas K. Karikari
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