Evidence map›Paper›PMID 40820870›Full record

ArticleHuman brain mapping2025

Mind the Gap: Does Brain Age Improve Alzheimer's Disease Prediction?

Trevor Wei Kiat Tan, Kim-Ngan Nguyen, Chen Zhang, Ru Kong, Susan F Cheng, Fang Ji, Joanna Su Xian Chong, Eddie Jun Yi Chong, Narayanaswamy Venketasubramanian, Csaba Orban and 6 more

Abstract read
In one paragraph

Article in Human brain mapping, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Alzheimer's Disease Brain Phenotypes are Age-dependent.bioRxiv : the preprint server for biology · 2026
    Article
  2. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors.

Trevor Wei Kiat Tan *Centre for Sleep and Cognition & Centre for Translational MR Research, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.ORCID https://orcid.org/0000-0002-3732-4768
Kim-Ngan Nguyen *Centre for Sleep and Cognition & Centre for Translational MR Research, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.ORCID https://orcid.org/0009-0004-5968-6307
Chen ZhangCentre for Sleep and Cognition & Centre for Translational MR Research, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.ORCID https://orcid.org/0000-0002-1579-0047
Ru KongCentre for Sleep and Cognition & Centre for Translational MR Research, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.ORCID https://orcid.org/0000-0001-7842-0329
Susan F ChengCentre for Sleep and Cognition & Centre for Translational MR Research, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.ORCID https://orcid.org/0000-0002-1201-2880
Fang JiCentre for Sleep and Cognition & Centre for Translational MR Research, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.ORCID https://orcid.org/0000-0002-7471-0115
Joanna Su Xian ChongCentre for Sleep and Cognition & Centre for Translational MR Research, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.ORCID https://orcid.org/0009-0008-5077-5206
Eddie Jun Yi ChongMemory, Aging and Cognition Centre, National University Health System, Singapore, Singapore.
Narayanaswamy VenketasubramanianRaffles Neuroscience Centre, Raffles Hospital, Singapore, Singapore.ORCID https://orcid.org/0000-0003-3593-6362
Csaba OrbanCentre for Sleep and Cognition & Centre for Translational MR Research, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.ORCID https://orcid.org/0000-0001-9133-3561
Michael W L CheeCentre for Sleep and Cognition & Centre for Translational MR Research, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.ORCID https://orcid.org/0000-0002-6087-0548
Christopher ChenMemory, Aging and Cognition Centre, National University Health System, Singapore, Singapore.ORCID https://orcid.org/0000-0002-1047-9225
Juan Helen ZhouCentre for Sleep and Cognition & Centre for Translational MR Research, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.ORCID https://orcid.org/0000-0002-0180-8648
B T Thomas YeoCentre for Sleep and Cognition & Centre for Translational MR Research, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.ORCID https://orcid.org/0000-0002-0119-3276
Alzheimer's Disease Neuroimaging Initiative
Australian Imaging Biomarkers and Lifestyle Study of Aging

Funding

Alzheimer's Disease Neuroimaging Initiative - SupplementU01AG024904 · NIA · NORTHERN CALIFORNIA INSTITUTE RES &EDUC · PI WEINER, MICHAEL W · 2004 to 2015
$121.0M
A mega-analysis framework for delineating autism neurosubtypesR01MH133334 · NIMH · CHILD MIND INSTITUTE, INC. · PI Adriana Di Martino · 2023 to 2026
$2.9M
Ministry of Health -Singapore CG21APR1009NIA NIH HHS U01 AG024904NIH HHS R01MH133334NIMH NIH HHS R01 MH133334NUS Yong Loo Lin School of Medicine NUHSRO/2020/124/TMR/LOASingapore National Medical Research Council CTGIIT23jan-0001Singapore National Medical Research Council OFIRG24jan-0030Singapore National Medical Research Council OFIRG24jul-0049Singapore National Medical Research Council OFLCG19May-0035Singapore National Medical Research Council STaR20nov-0003
6 · The paper itself

Abstract

Brain age is widely regarded as a powerful marker of general brain health. Brain age models are typically trained on large datasets to predict chronological age, which may offer advantages in predicting specific health outcomes, much like the success of finetuning large language models for specific applications. However, it is also well accepted that machine learning models trained to directly predict specific outcomes (i.e., direct models) often outperform those trained on surrogate objectives. Therefore, despite their much larger training data, it is unclear whether brain age models outperform direct models in predicting specific brain health outcomes. Here, we compare large-scale brain age models (pretrained on 53,542 participants) and direct models for predicting specific health outcomes related to Alzheimer's disease (AD) dementia. Using anatomical T1 scans from three continents (N = 1,848), we find that summarizing brain age with a single scalar (i.e., brain age gap) led to poor prediction performance. Using higher-dimensional intermediate representations of brain age models led to better prediction, but was still worse than direct models without finetuning. Using intermediate representations of finetuned brain age models was necessary to achieve similar performance to direct models. Overall, our results do not discount brain age as a useful marker of general brain health but suggest that using chronological age as a pretraining target might be suboptimal for predicting specific health outcomes.

Indexed as

AgingAlzheimer DiseaseBrainMachine LearningModels, NeurologicalAgedAged, 80 and overFemaleHumansMagnetic Resonance ImagingMaleMiddle Aged

Identifiers

PMID40820870
PMCPMC12358809

What OpenQuestion holds

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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 OpenQuestion graph.