Evidence map›Paper›PMID 41523182›Full record

ArticleBrain communications2026

Enhanced monitoring of Alzheimer's disease brain atrophy using composite value ratios of volumes.

Isaac Llorente-Saguer, Neil P Oxtoby

Abstract read
In one paragraph

Article in Brain communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Isaac Llorente-SaguerUCL Hawkes Institute and Department of Medical Physics and Biomedical Engineering, University College London, London, WC1E 6BT, UK.ORCID https://orcid.org/0000-0002-7612-5331
Neil P OxtobyUCL Hawkes Institute and Department of Computer Science, University College London, London, WC1E 6BT, UK.ORCID https://orcid.org/0000-0003-0203-3909

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Brain atrophy is a natural consequence of ageing but can be accelerated by neurodegenerative diseases such as Alzheimer's disease. We apply an existing algorithm to identify new biomarkers that better track volumetric changes over time, i.e. atrophy. These new biomarkers are the volumetric ratio of two composite regions of interest, identified by an algorithm optimized to enhance the monitoring of Alzheimer's disease progression. The algorithm prioritizes biomarkers with less noisy trajectories (quantified by lower sample size estimates for clinical trials) and that capture disease signal by showing a greater rate of change in amyloid-positive versus amyloid-negative individuals, ensuring the biomarker effectively reflects Alzheimer's pathology. Data from 1381 individuals from the Alzheimer's Disease Neuroimaging Initiative database having multiple MRI scans were analysed. The new biomarkers outperformed traditional volumetric measures (whole brain, hippocampus and ventricles) across all metrics. This improvement was particularly pronounced in cognitively impaired individuals, where atrophy is more severe. Among the traditional measures, ventricular volume had the best performance. Results suggest that ratios of regional brain volumes could enhance disease progression tracking, as has been shown in other modalities like fluid biomarker ratios and standardized uptake value ratios from positron emission tomography.

Indexed as

CIcognitively impairedcognitively unimpairedcomposite value ratioCUCVRICVintracranial volumesample size estimateSSE

Identifiers

PMID41523182
PMCPMC12782101

What Socratic holds

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LicenceCC BY
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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 Socratic graph.