Evidence map›Paper›PMID 41748878›Full record

ArticleCommunications medicine2026

Predicting rates of cognitive and functional decline in Alzheimer's disease and mild cognitive impairment.

Antigone Fogel, Chloe Walsh, Nan Fletcher-Lloyd, Paresh Malhotra, Mina Ryten, Ramin Nilforooshan, Payam Barnaghi

Abstract read
In one paragraph

Article in Communications medicine, 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

7 authors.

Antigone FogelDepartment of Brain Sciences, Imperial College London, London, UK. antigone.fogel23@imperial.ac.uk.ORCID http://orcid.org/0009-0004-7142-4406
Chloe WalshDepartment of Brain Sciences, Imperial College London, London, UK.ORCID http://orcid.org/0009-0009-0516-9634
Nan Fletcher-LloydDepartment of Brain Sciences, Imperial College London, London, UK.ORCID http://orcid.org/0000-0003-2002-5945
Paresh MalhotraDepartment of Brain Sciences, Imperial College London, London, UK.ORCID http://orcid.org/0000-0002-1897-0780
Mina RytenDepartment of Clinical Neurosciences, University of Cambridge, Cambridge, UK.
Ramin NilforooshanDepartment of Brain Sciences, Imperial College London, London, UK.
Payam BarnaghiDepartment of Brain Sciences, Imperial College London, London, UK. p.barnaghi@imperial.ac.uk.ORCID http://orcid.org/0000-0001-8591-9638

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe global population of People Living with Dementia (PLWD) is expected to grow rapidly in the coming decades, increasing the need for personalised, generalisable, and scalable prognosis and care planning support. However, current prognostic guidance does not adequately capture the heterogeneity in dementia trajectories, and existing predictive models of dementia progression rely on costly and inaccessible data, limiting their scalability in resource-constrained settings.

methodsUsing clinical assessments, demographic, and medical history data from 153 12-month clinical trajectories collected over three years, two machine learning algorithms were developed to predict 12-month cognitive and functional decline in Alzheimer's Disease (AD) and Mild Cognitive Impairment (MCI). Models were externally validated on 741 trajectories from the ADNI cohort. Cognitive and functional decline were estimated using the Mini-Mental State Exam (MMSE) and Bristol Activities of Daily Living (BADL).

resultsThe MMSE model achieves a mean absolute error (MAE) of 1.84 (95% CI: 1.64-2.04) internally and 2.19 in external validation. The BADL model achieves an MAE of 3.88 (95% CI: 3.46-4.30). Baseline scores on ideational praxis, orientation, and word recall are among the strongest predictors of cognitive decline, while independence in food preparation, finances, and dressing are among the top predictors of functional decline.

conclusionsOur models use only routinely collected and easily accessible data, offering high translational potential. If implemented, our scalable, data-driven prognostic support tool could streamline clinical workflows, support personalised care planning, and provide PLWD and their families with greater clarity and reassurance.

Identifiers

PMID41748878
PMCPMC13061986

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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.