Trajectories of plasma and CSF MTBR-tau243 and phosphorylated-tau species across the Alzheimer’s disease continuum
Lyduine Eisa Collij; Gemma Salvadó; Kanta Horie; Nicolas R. Barthélemy; Tobey J. Betthauser; Olof T. Strandberg; Ruben A Smith; Sebastian Palmqvist · 2026 · Nature Communications
WASTE classifies this as Negative / Null Result Report · AI classification, approximate
The study found no significant effect — useful as a negative control or null benchmark for your own design.
Abstract
To efficiently implement plasma and cerebrospinal fluid (CSF) biomarkers for staging and prognosis of Alzheimer disease (AD), we must understand their dynamics across disease progression. We analyzed participants from the Swedish BioFINDER-2 study with mass spectrometry measurements of plasma and CSF tau species, including eMTBR-tau243/MTBR-tau243 and phosphorylation occupancies (%p-tau). Disease duration was estimated using Aβ-PET and tau-PET with the SILA algorithm. Bootstrapped LOESS models showed that %p-tau217 changes earliest, increasing just before Aβ-PET positivity. Other p-tau species
Abstract by Lyduine Eisa Collij; Gemma Salvadó; Kanta Horie; Nicolas R. Barthélemy; Tobey J. Betthauser; Olof T. Strandberg; Ruben A Smith; Sebastian Palmqvist, Nature Communications (2026) — licensed CC BY 4.0.
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Metadata source: OpenAlex · DOI 10.1038/s41467-026-71732-1
