Evidence map›Paper›PMID 41885175›Full record

ArticleBrain : a journal of neurology2026

Longitudinal trajectories of divergent cortical tau patterns in preclinical Alzheimer's disease.

Christina B Young, Jintao Sheng, Joseph R Winer, Karly Cody, Isha Sai, Mackenzie L Carlson, Kyan Younes, Philip S Insel, Aaron P Schultz, Elizabeth C Mormino

Abstract read
In one paragraph

Article in Brain : a journal of neurology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

10 authors.

Christina B YoungDepartment of Neurology and Neurological Sciences, Stanford University School of Medicine, Palo Alto, CA 94304, USA.ORCID 0000-0001-9535-2137
Jintao ShengDepartment of Neurology and Neurological Sciences, Stanford University School of Medicine, Palo Alto, CA 94304, USA.
Joseph R WinerDepartment of Neurology and Neurological Sciences, Stanford University School of Medicine, Palo Alto, CA 94304, USA.ORCID 0000-0003-4069-3158
Karly CodyDepartment of Neurology and Neurological Sciences, Stanford University School of Medicine, Palo Alto, CA 94304, USA.ORCID 0000-0001-5996-2560
Isha SaiDepartment of Neurology and Neurological Sciences, Stanford University School of Medicine, Palo Alto, CA 94304, USA.
Mackenzie L CarlsonDepartment of Neurology and Neurological Sciences, Stanford University School of Medicine, Palo Alto, CA 94304, USA.
Kyan YounesDepartment of Neurology and Neurological Sciences, Stanford University School of Medicine, Palo Alto, CA 94304, USA.
Philip S InselDepartment of Psychiatry and Behavioral Sciences, University of California San Francisco, San Francisco, CA 94143, USA.ORCID 0000-0001-6026-2238
Aaron P SchultzDepartment of Neurology, Massachusetts General Hospital, Boston, MA 02114, USA.
Elizabeth C MorminoDepartment of Neurology and Neurological Sciences, Stanford University School of Medicine, Palo Alto, CA 94304, USA.

Funding

Stanford Alzheimer's Disease Research CenterAdmin Supp: Developing iPSC models for AD and PDP30AG066515 · NIA · STANFORD UNIVERSITY · PI Lisa Goldman Rosas · 2020 to 2026
$29.0M
Hippocampal-dependent memory decline in aging and early Alzheimer's diseaseR01AG074339 · NIA · STANFORD UNIVERSITY · PI ELIZABETH MORMINO · 2022 to 2026
$6.0M
High-resolution imaging of hippocampal mechanisms in age-related memory decline.R01AG048076 · NIA · STANFORD UNIVERSITY · PI WAGNER, ANTHONY D · 2014 to 2018
$1.9M
Regional tau deposition and digital assessment of cognition in preclinical AD and MCIR00AG071837 · NIA · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Christina B Young · 2025 to 2026
$606k
NIA NIH HHS P30 AG066515NIA NIH HHS R00 AG071837NIA NIH HHS R01 AG048076NIA NIH HHS R01 AG074339
6 · The paper itself

Abstract

Approximately 10% of clinically unimpaired individuals with abnormal amyloid (A+; preclinical Alzheimer's disease) have "divergent" cortical tau pathology (A+TCortical+), defined as greater than expected tau in cortical regions relative to medial temporal lobe and/or cortical asymmetry on tau PET in addition to or instead of traditional medial temporal lobe tau burden. Although these A+TCortical+ individuals have subtle cognitive deficits at baseline, the longitudinal imaging and clinical outcomes are unknown. We aimed to characterize longitudinal trajectories of A+TCortical+ individuals compared to other biomarker-defined clinically unimpaired groups given that identifying those at highest risk for decline is critical for informing prevention trials and understanding early disease mechanisms. In this longitudinal study, we examined tau PET, MRI, cognitive, and functional data from 395 clinically unimpaired participants, ages 65 to 85 years, enrolled in the Anti-Amyloid Treatment in Asymptomatic AD (A4) Study. Participants had 2-5 flortaucipir scans over a mean (standard deviation) follow-up period of 4.7 (1.6) years. Change in regional and voxelwise tau patterns, atrophy, cognition, and functioning were examined. Longitudinal trajectories from A+TCortical+ (n=34) were compared to preclinical Alzheimer's disease with elevated tau PET signal in medial temporal lobe only (A+TMTL+, n=102), preclinical Alzheimer's disease without significant tau (A+TMTL-, n=210), and those without amyloid or tau (A-TMTL-, n=49). Cortical tau accumulation was fastest in A+TCortical+ (0.018-0.034 standardized uptake value ratios per year), whereas medial temporal lobe tau accumulation was comparable across A+TCortical+, A+TMTL+, and A+TMTL- groups (0.010-0.013 standardized uptake value ratios per year). Tau continued to accumulate in affected regions and contralateral homotopic regions in A+TCortical+ participants with asymmetrical tau at baseline such that asymmetrical patterns were maintained over time. Younger A+TCortical+ participants had an especially fast cortical accumulation rate. The A+TCortical+ group showed significantly greater neurodegeneration and faster clinical decline (Clinical Dementia Rating Scale Sum of Boxes = 0.610 points per year; Mini-Mental State Examination = -0.780 points per year) than all other biomarker-defined subgroups (Clinical Dementia Rating Scale Sum of Boxes = 0.048-0.182 points per year; Mini-Mental State Examination = -0.189-0.006 points per year). In summary, individuals with divergent cortical tau patterns continue to accumulate cortical tau at a faster rate, show greater neurodegeneration, and have faster cognitive and functional decline than other preclinical Alzheimer's disease subgroups. Clinical trials and research examining tau progression and clinical decline in preclinical Alzheimer's disease without subtyping may be disproportionately influenced by this small, high-risk subgroup.

Indexed as

atypical patternscortical taulongitudinal taupreclinical ADtau PET

Identifiers

PMID41885175
PMCPMC13142817

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.