Evidence map›Paper›PMID 40440591›Full record

Trial reportNeurology2025

Changes in Daily Functioning in Association With Tau and Amyloid Among Unimpaired Older Adults With and Without Elevated Amyloid.

Mark A Dubbelman, Andy Liu, Michael C Donohue, Oliver Langford, Rema Raman, Dorene M Rentz, Rebecca Amariglio, Reisa Anne Sperling, Paul S Aisen, Gad A Marshall and 1 more

2 registry-linked trialsAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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.

NCT02008357 phase3completednot on this map

Anti-Amyloid Treatment in Asymptomatic Alzheimer's Disease (A4 Study)

TypeinterventionalSponsorEli Lilly and CompanyRan2014 to 2023Enrolled1,169ConditionsCognition DisordersArmsPlacebo, Solanezumab
NCT02488720 completednot on this map

Longitudinal Evaluation of Amyloid Risk and Neurodegeneration - the LEARN Study. A Companion Observational Study to Anti-Amyloid Treatment in Asymptomatic Alzheimer's Disease (A4) Trial

TypeobservationalSponsorUniversity of Southern CaliforniaRan2015 to 2023Enrolled538ConditionsCognition Disorders
3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. APOE and amyloid-tau pathology in cognitively unimpaired older adults.medRxiv : the preprint server for health sciences · 2026
    Article
  2. Article
  3. Unraveling the Effects ofInternational journal of molecular sciences · 2025
    Review
  4. APOE and amyloid-tau pathology in cognitively unimpaired older adults.Alzheimer's & dementia (Amsterdam, Netherlands)
    Article
  5. 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

11 authors.

Mark A DubbelmanCenter for Alzheimer Research and Treatment, Department of Neurology, Brigham and Women's Hospital, Harvard Medical School.ORCID 0000-0002-5708-4925
Andy LiuAlzheimer Therapeutic Research Institute, Keck School of Medicine, University of Southern California, San Diego, CA.ORCID 0009-0004-0319-256X
Michael C DonohueAlzheimer Therapeutic Research Institute, Keck School of Medicine, University of Southern California, San Diego, CA.ORCID 0000-0001-6026-2238
Oliver LangfordAlzheimer Therapeutic Research Institute, Keck School of Medicine, University of Southern California, San Diego, CA.ORCID 0009-0006-8951-1326
Rema RamanAlzheimer Therapeutic Research Institute, Keck School of Medicine, University of Southern California, San Diego, CA.ORCID 0000-0002-4096-6390
Dorene M RentzCenter for Alzheimer Research and Treatment, Department of Neurology, Brigham and Women's Hospital, Harvard Medical School.ORCID 0000-0002-6318-9213
Rebecca AmariglioCenter for Alzheimer Research and Treatment, Department of Neurology, Brigham and Women's Hospital, Harvard Medical School.ORCID 0009-0009-5878-8930
Reisa Anne SperlingCenter for Alzheimer Research and Treatment, Department of Neurology, Brigham and Women's Hospital, Harvard Medical School.ORCID 0000-0003-1535-6133
Paul S AisenAlzheimer Therapeutic Research Institute, Keck School of Medicine, University of Southern California, San Diego, CA.ORCID 0000-0002-2896-5838
Gad A MarshallCenter for Alzheimer Research and Treatment, Department of Neurology, Brigham and Women's Hospital, Harvard Medical School.ORCID 0000-0002-9096-2355
as the A4 Study team

Funding

Anti-Amyloid Treatment in Asymptomatic Alzheimer's Disease (A4) Open-Label Extension StudyR01AG063689 · NIA · BRIGHAM AND WOMEN'S HOSPITAL · PI AISEN, PAUL S., SPERLING, REISA A. · 2019 to 2024
$30.8M
NIA NIH HHS R01 AG063689
6 · The paper itself

Abstract

BACKGROUND AND

objectivesEveryday functioning declines gradually over time in Alzheimer disease (AD), with the earliest changes potentially occurring at the preclinical stage. We investigated how changes in everyday functioning relate to (changes in) amyloid and tau in a large sample of cognitively unimpaired older adults, most of whom had elevated amyloid levels at the start of the study.

methodsThis prospective study included participants from a 240-week randomized controlled trial of an anti-amyloid drug, solanezumab, and individuals who screen-failed because of a negative amyloid PET scan. A subset (n = 434) underwent repeated tau PET scans. Participants and their study partners completed the Alzheimer's Disease Cooperative Study Activities of Daily Living Prevention Instrument multiple times during the double-blind phase of the trial. Using generalized least-squares models, fit by restricted maximum likelihood, we analyzed how changes in everyday functioning related to amyloid and tau PET. We also correlated changes in amyloid and tau PET with changes in everyday functioning.

resultsA total of 1,707 participants (71.5 ± 4.7 years, 60% female) showed a marginal decline in everyday functioning. Among individuals with elevated amyloid, those with the highest levels of neocortical and medial temporal tau showed the largest decline in everyday functioning, as reported by the participants and their study partners. Increases in neocortical and medial temporal tau correlated moderately (correlation coefficient ranging from -0.2 to -0.5) with a decline in ADCS ADL-PI scores. Functional changes were not evident with amyloid alone. At the item level, participants and their study partners were most likely to report increased difficulty at the last visit with completing complex activities and selecting and paying for items when shopping. DISCUSSION: Higher tau levels are associated with the fastest decline in everyday functioning in the presence of elevated amyloid, and those accumulating more tau show a faster decline in everyday functioning. These findings demonstrate the utility of including sensitive measures of everyday functioning in clinical practice and clinical trials at the stage of preclinical AD. TRIAL REGISTRATION INFORMATION: The A4 study, ClinicalTrials.gov ID: NCT02008357; and Longitudinal Evaluation of Amyloid Risk and Neurodegeneration, ClinicalTrials.gov ID: NCT02488720.

Indexed as

Activities of Daily LivingAlzheimer DiseaseAmyloid beta-PeptidesBraintau ProteinsAgedAged, 80 and overAntibodies, Monoclonal, HumanizedDouble-Blind MethodFemaleHumansMalePositron-Emission TomographyProspective StudiesAmyloid beta-PeptidesAntibodies, Monoclonal, Humanizedsolanezumabtau Proteins

Identifiers

PMID40440591
PMCPMC12123750

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

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 Socratic graph.