Back

Prognostic value of plasma brain-derived pTau

Ghisays, V.; Denkinger, M. N.; Singh, A.; Marques, T. M.; Malek-Ahmadi, M.; Van-Keuren Jensen, K.; Protas, H. D.; Sohankar, J.; Goradia, D. D.; Devadas, V.; Chen, Y.; Li, S.; Langbaum, J. B.; Weiner, M. W.; Reiman, E. M.; Su, Y.; Ashton, N. J.; Alzheimer's Disease Neuroimaging Initiative,

2026-06-30 neurology
10.64898/2026.06.26.26356597 medRxiv
Show abstract

Background: Plasma brain-derived pTau217(BD-pTau217) may provide a Alzheimers disease-specific plasma tau measure than total pTau217, but its prognostic value is unclear. We compared BD-pTau217 and total plasma pTau217 for predicting clinical and amyloid PET progression in cognitively unimpaired (CU) ADNI participants. Methods: Plasma NULISAseq biomarkers were measured in 1,427 ADNI participants, including 529 CU individuals. Amyloid PET progression was assessed in baseline CU amyloid-negative participants (Centiloid [≥] 24.1) with longitudinal PET imaging; clinical progression was assessed in all baseline CU participants. Associations were evaluated using Cox models and time-dependent AUC. Results: BD-pTau217 did not clearly outperform total pTau217 for predicting progression to mild cognitive impairment or dementia. However, among baseline amyloid-negative participants (N=175), BD-pTau217 better predicted amyloid PET positivity at 2.5 years (tdAUC 0.82 vs 0.69; HR=10.54, p=0.00015) and 4 years (tdAUC 0.77 vs 0.64; HR=7.03, p=0.00055). Conclusion: BD-pTau217 improved prediction of near-term amyloid PET progression, with less clear advantage for clinical progression.

Matching journals

The top 1 journal accounts for 50% of the predicted probability mass.