Evidence map›Paper›PMID 40750514›Full record

ArticleThe journal of prevention of Alzheimer's disease2025

Temporal associations of neuropsychiatric symptoms, demographics and amyloid with subsequent tau burden in older adults.

Pablo Aguilar-Dominguez, Eleni Palpatzis, Muge Akinci, Anna Canal-Garcia, Joana B Pereira, Alexandre Bejanin, Eider M Arenaza-Urquijo, Alzheimer’s Disease Neuroimaging Initiative

Abstract read
In one paragraph

Article in The journal of prevention of Alzheimer's disease, 2025. 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. Review
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

8 authors.

Pablo Aguilar-DominguezBarcelona Institute for Global Health (ISGlobal), Environment and Health over the Lifecourse programme. Barcelona, Spain; University of Pompeu Fabra (UPF), Barcelona, Spain; Sant Pau Memory Unit, IR SANT PAU, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
Eleni PalpatzisBarcelona Institute for Global Health (ISGlobal), Environment and Health over the Lifecourse programme. Barcelona, Spain; University of Pompeu Fabra (UPF), Barcelona, Spain.
Muge AkinciBarcelona Institute for Global Health (ISGlobal), Environment and Health over the Lifecourse programme. Barcelona, Spain; University of Pompeu Fabra (UPF), Barcelona, Spain.
Anna Canal-GarciaDivision of Neuro, Department of Clinical Neurosciences, Karolinska Institutet, Stockholm, Sweden.
Joana B PereiraDivision of Neuro, Department of Clinical Neurosciences, Karolinska Institutet, Stockholm, Sweden.
Alexandre BejaninSant Pau Memory Unit, IR SANT PAU, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain; Center of Biomedical Investigation Network for Neurodegenerative Diseases (CIBERNED), Madrid, Spain.
Eider M Arenaza-UrquijoBarcelona Institute for Global Health (ISGlobal), Environment and Health over the Lifecourse programme. Barcelona, Spain. Electronic address: eider.arenaza@isglobal.org.
Alzheimer’s Disease Neuroimaging Initiative

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPsychiatric symptoms are increasingly recognized as early manifestations of Alzheimer's disease (AD). These symptoms may reflect or contribute to underlying neurobiological changes, including tau burden, which represents more advanced AD pathology. Understanding factors associated with tau burden may help identify individuals at elevated risk and improve early detection strategies.

objectivesTo investigate the temporal relationships between neuropsychiatric symptoms, demographic factors, and tau burden, by examining amyloid (Aβ)-dependent, -independent, and interactive associations.

designRetrospective cohort study.

settingAlzheimer's Disease Neuroimaging Initiative.

participantsWe included 681 participants without dementia (mean age = 71.2 years, 51.8 % female). MEASUREMENTS: The participants underwent tau PET scanning with prior amyloid PET and Neuropsychiatric Inventory (NPI) interview assessments clustered around three time periods relative to tau PET: closest (0 - 2 years), mid (3 - 5 years), and furthest (6 - 8 years). Linear regression analyses, adjusting for age and APOE ε4 alleles, examined associations of NPI scores, sex, education, and their Aβ-status interactions with tau burden.

resultsHigher total NPI scores up to 2 years prior to tau PET were associated with greater tau burden independently of Aβ status, whereas anxiety symptoms demonstrated an Aβ-dependent relationship with tau. (NPI: β=0.117, 95 % CI: 0.049 to 0.185, p=0.001, Anxiety: β=0.249, 95 % CI: 0.073 to 0.424, p=0.006). NPI measured up to 5 years prior to tau PET interacted with Aβ on tau burden (0-2 years: β=0.272, 95 % CI: 0.136 to 0.407, p<0.001, 3-5 years: β=0.336, 95 % CI: 0.127 to 0.544, p=0.002). Sex and education showed minimal associations with tau at uncorrected statistical levels.

conclusionsNeuropsychiatric symptoms were associated with tau burden up to two years before tau sampling, independently of Aβ, and interacted with Aβ status up to five years prior, suggesting that neuropsychiatric symptoms are related to tau in the short term and may represent manifestations of advancing AD pathology. Demographic factors showed minimal associations. These findings highlight the importance of evaluating neuropsychiatric and anxiety symptoms as potential indicators of increased tau pathology.

Indexed as

Alzheimer DiseaseAmyloid beta-PeptidesBraintau ProteinsAgedAged, 80 and overFemaleHumansMaleNeuropsychological TestsPositron-Emission TomographyRetrospective StudiesAmyloid beta-Peptidestau ProteinsAlzheimer’s diseaseAmyloidNeuropsychiatric symptomsTau

Identifiers

PMID40750514
PMCPMC12501339

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.