Evidence map›Paper›PMID 41256144›Full record

ArticlemedRxiv : the preprint server for health sciences2025

Trajectories of plasma biomarkers, amyloid-beta burden and cognitive decline in Alzheimer's disease: A Longitudinal ADNI Study.

Yara Yakoub, Ting Qiu, Clémence Peyrot, Gemma Salvadó, Sylvia Villeneuve, Alexa Pichet Binette

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Yara YakoubDouglas Mental Health University Institute, Montreal, Quebec, Canada. Address: 6875 Blvd. LaSalle, Verdun, H4H 1R3, Québec, Canada.ORCID 0000-0002-4769-7162
Ting QiuDouglas Mental Health University Institute, Montreal, Quebec, Canada. Address: 6875 Blvd. LaSalle, Verdun, H4H 1R3, Québec, Canada.ORCID 0009-0007-8209-4424
Clémence PeyrotCentre de Recherche de l'Institut Universitaire de Gériatrie de Montréal, Montréal, Québec, Canada. Address: 4565 Queen Mary Rd, Montreal, H3W 1W5, Quebec, Canada.
Gemma SalvadóBarcelonaβeta Brain Research Centre (BBRC), Pasqual Maragall Foundation, Barcelona, Spain. Address: Carrer de Wellington, 30, Sant Martí, 08005 Barcelona, Spain.ORCID 0000-0002-5210-9230
Sylvia VilleneuveDouglas Mental Health University Institute, Montreal, Quebec, Canada. Address: 6875 Blvd. LaSalle, Verdun, H4H 1R3, Québec, Canada.ORCID 0000-0003-2338-0467
Alexa Pichet BinetteCentre de Recherche de l'Institut Universitaire de Gériatrie de Montréal, Montréal, Québec, Canada. Address: 4565 Queen Mary Rd, Montreal, H3W 1W5, Quebec, Canada.ORCID 0000-0001-5218-3337

Funding

Project 1U19AG024904 · NIA · NORTHERN CALIFORNIA INSTITUTE/RES/EDU · PI Duygu Tosun-Turgut · 2016 to 2026
$226.7M
National Centralized Repository for Alzheimer's Disease and Related Dementias (NCRAD)U24AG021886 · NIA · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI TATIANA M. FOROUD · 2002 to 2026
$119.8M
NIA NIH HHS U19 AG024904NIA NIH HHS U24 AG021886
6 · The paper itself

Abstract

As novel amyloid-β targeted therapies emerge, plasma biomarkers have promising potential to serve as screening tools and as surrogate measures for treatment outcomes. Understanding longitudinal trajectories of these biomarkers and how their changes relate to changes in AD pathology and cognition is needed to help track treatment response and guide patient care. We analyzed data from 394 individuals in the ADNI-FNIH dataset who had plasma biomarkers available across 14 assays, Aβ-PET scans and cognitive assessments over a 10-year period. Plasma p-tau217, regardless of the assay used, had the greatest rate of change over time. This increase was related to concurrent increase in Aβ-PET burden only in individuals with low levels of Aβ. The rate of p-tau217 change, rather than its baseline level, was the strongest predictor of future Aβ-PET positivity. On the other hand, in individuals with elevated levels of Aβ, higher rate of change in p-tau217 was associated with faster cognitive decline. These findings highlight a "dual" role of plasma p-tau217 rate of change, being either predictive of accumulating Aβ pathology at early stages and of cognitive decline at later stages of the AD continuum.

Identifiers

PMID41256144
PMCPMC12622140

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.