Evidence map›Paper›PMID 40705053›Full record

ArticleAge and ageing2025

Development and validation of a model to predict the progression of Alzheimer's disease.

Chenyin Chu, Yihan Wang, Andrew L H Huynh, Ka Weng Ng, Shu Liu, Guangyan Ji, James Doecke, Jurgen Fripp, Colin L Masters, Benjamin Goudey and 2 more

Abstract readValidation Study
In one paragraph

Article in Age and ageing, 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. 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

12 authors.

Chenyin ChuFaculty of Medicine, Nursing and Health Sciences, Monash University, Melbourne, Victoria, Australia.
Yihan WangFaculty of Medicine, Nursing and Health Sciences, Monash University, Melbourne, Victoria, Australia.
Andrew L H HuynhDepartment of Medicine, Austin Health, Heidelberg, Victoria, Australia.
Ka Weng NgFlorey Department of Neuroscience and Mental Health, The University of Melbourne, Melbourne, Victoria, Australia.
Shu LiuFlorey Department of Neuroscience and Mental Health, The University of Melbourne, Melbourne, Victoria, Australia.
Guangyan JiFlorey Institutes of Neuroscience and Mental Health, Melbourne, Victoria, Australia.
James DoeckeAustralian E-Health Research Centre, CSIRO, Herston, Queensland, Australia.ORCID 0000-0003-2863-0293
Jurgen FrippAustralian E-Health Research Centre, CSIRO, Herston, Queensland, Australia.
Colin L MastersFlorey Institutes of Neuroscience and Mental Health, Melbourne, Victoria, Australia.ORCID 0000-0003-3072-7940
Benjamin GoudeyFlorey Institutes of Neuroscience and Mental Health, Melbourne, Victoria, Australia.ORCID 0000-0002-2318-985X
Liang JinFaculty of Medicine, Nursing and Health Sciences, Monash University, Melbourne, Victoria, Australia.
Yijun PanFaculty of Medicine, Nursing and Health Sciences, Monash University, Melbourne, Victoria, Australia.ORCID 0000-0002-1442-3333

Funding

Alzheimer's Association, USA 23AARF-1020292National Health and Medical Research Council, Australia GNT2007912, GNT2022203
6 · The paper itself

Abstract

backgroundCognition monitoring is crucial for care planning in people with mild cognitive impairment (MCI) and Alzheimer's dementia (AD).

objectiveTo develop a machine learning model to assist cognition monitoring.

designFlorey Fusion Model (FFM) was constructed and validated in two phases: (i) model development and cross-validation using data collected via the Australian Imaging, Biomarker, and Lifestyle of Ageing (AIBL) study, and (ii) simulation and missing data trials with 30 new participants.

methodsThis prognostic study recruited 238 participants in the AIBL study. Support vector machine, gradient boosting and random forest were trialled to develop the FFM. Cognitive decline was assessed via changes in Clinical Dementia Rating Sum of Boxes (CDR-SB) and Mini-Mental State Examination (MMSE) scores. Model performance was evaluated by cross validation and compared against baseline models.

resultsThe FFM achieved a median area under receive character curve (AUC-ROC) of 0.91 (IQR 0.87-0.93) for MCI-to-AD progression prediction. A mean absolute error (MAE) of 1.32 (IQR 1.30-1.33) for CDR-SB and 1.51 (IQR 1.50-1.52) for MMSE was achieved for 3-year cognition forecast. Simulation and missing data trials yielded up to 94% accuracy for MCI-to-AD conversion and MAEs of 1.27-2.12 for CDR-SB score prediction.

conclusionThe FFM holds the potential to facilitate cognition monitoring in people with MCI/AD; however, a larger trial will be required to refine it as a clinical grade tool.

Indexed as

Alzheimer DiseaseCognitionCognitive DysfunctionMachine LearningAgedAged, 80 and overAustraliaDisease ProgressionFemaleHumansMaleMental Status and Dementia TestsPredictive Value of TestsPrognosisReproducibility of ResultsAlzheimer’s diseasecognition monitoringmachine learningmild cognitive impairmentolder people

Identifiers

PMID40705053
PMCPMC12288498

What Socratic holds

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LicenceCC BY-NC-ND
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Registered trials

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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 Socratic graph.