Evidence map›Paper›PMID 40897577›Full record

ArticleThe journal of prevention of Alzheimer's disease2025

Preclinical detection of Alzheimer's disease pathology using conceptual discrimination abilities.

Lara Huyghe, Yasmine Salman, Lise Colmant, Thomas Gérard, Vincent Malotaux, Gabriel Besson, Emma Delhaye, Christine Bastin, Quentin Dessain, Laurence Dricot and 4 more

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. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

14 authors.

Lara HuygheInstitute of Neuroscience (IoNS), UCLouvain, Brussels, Belgium. Electronic address: lara.huyghe@uclouvain.be.
Yasmine SalmanInstitute of Neuroscience (IoNS), UCLouvain, Brussels, Belgium. Electronic address: yasmine.salman@uclouvain.be.
Lise ColmantInstitute of Neuroscience (IoNS), UCLouvain, Brussels, Belgium; Neurology Department, Saint-Luc University Hospital, Brussels, Belgium. Electronic address: lise.colmant@uclouvain.be.
Thomas GérardInstitute of Neuroscience (IoNS), UCLouvain, Brussels, Belgium; Nuclear Medicine Department, Saint-Luc University Hospital, Brussels, Belgium. Electronic address: thomas.gerard@uclouvain.be.
Vincent MalotauxInstitute of Neuroscience (IoNS), UCLouvain, Brussels, Belgium; Psychiatry Department, Massachusetts General Hospital, Harvard Medical School, Boston, USA. Electronic address: vincent.malotaux@uclouvain.be.
Gabriel BessonGIGA-Cyclotron Research Center Human Imaging, University of Liège, Belgium. Electronic address: gabriel.besson@gmail.com.
Emma DelhayeGIGA-Cyclotron Research Center Human Imaging, University of Liège, Belgium; CICPSI, Faculty of Psychology, University of Lisbon, Portugal. Electronic address: emma.delhaye@uliege.be.
Christine BastinGIGA-Cyclotron Research Center Human Imaging, University of Liège, Belgium. Electronic address: christine.bastin@uliege.be.
Quentin DessainICTEAM, UCLouvain, Louvain-La-Neuve, Belgium. Electronic address: quentin.dessain@uclouvain.be.
Laurence DricotInstitute of Neuroscience (IoNS), UCLouvain, Brussels, Belgium. Electronic address: laurence.dricot@uclouvain.be.
Renaud LhommelInstitute of Neuroscience (IoNS), UCLouvain, Brussels, Belgium; Nuclear Medicine Department, Saint-Luc University Hospital, Brussels, Belgium. Electronic address: renaud.lhommel@saintluc.uclouvain.be.
Adrian IvanoiuInstitute of Neuroscience (IoNS), UCLouvain, Brussels, Belgium; Neurology Department, Saint-Luc University Hospital, Brussels, Belgium. Electronic address: adrian.ivanoiu@uclouvain.be.
Lisa QuenonInstitute of Neuroscience (IoNS), UCLouvain, Brussels, Belgium; Neurology Department, Saint-Luc University Hospital, Brussels, Belgium. Electronic address: lisa.quenon@uclouvain.be.
Bernard HanseeuwInstitute of Neuroscience (IoNS), UCLouvain, Brussels, Belgium; Neurology Department, Saint-Luc University Hospital, Brussels, Belgium; Radiology Department, Massachusetts General Hospital, Harvard Medical School, Boston, USA; WELBIO department, WEL Research Institute, avenue Pasteur, 6 1300 Wavre, Belgium. Electronic address: bernard.hanseeuw@uclouvain.be.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPerformance on the Conceptual Matching Task (CMT), a measure of discrimination between conceptually confusable items, has been suggested as a cognitive marker of rhinal cortex atrophy, one of the first brain regions affected by Alzheimer's disease (AD) pathology.

objectivesWe aimed to determine whether CMT can detect preclinical AD, and whether CMT performance is related to regional deposition of tau protein or other AD-associated lesions including amyloid (Aβ) accumulation and white matter hyperintensities (WMH). DESIGN, SETTING AND

participantsThis cross-sectional study include 101 participants from the UCL2016-121 cohorts in Brussels, Belgium, classified as 56 Aβ-negative cognitively unimpaired (Aβ-CU), 25 Aβ-positive CU (Aβ+CU, preclinical AD), and 20 Aβ-positive mildly cognitively impaired (Aβ+MCI, prodromal AD) individuals. MEASUREMENTS: Participants underwent CMT and a standard neuropsychological assessment that included the Preclinical Alzheimer Cognitive Composite (PACC5), an Aβ status examination, a 3D-T1 MRI and a [

resultsCMT performance was lower among Aβ+MCI and Aβ+CU than Aβ-CU individuals. The effect of Aβ on CMT performance was stronger in the presence of WMH, but rhinal tau burden did not explain CMT performance beyond the effects of Aβ and WMH. CMT performance correlated with executive, memory, and language performance. Finally, CMT was more sensitive than PACC5 to detect CU individuals with Aβ or tau pathology.

conclusionGiven that impaired performance is observed earlier in the CMT than in standard neuropsychological tests, this test shows promise as an early diagnostic tool for AD and may offer significant utility in the context of clinical trials.

Indexed as

Alzheimer DiseaseCognitive DysfunctionAgedAmyloid beta-PeptidesBrainCross-Sectional StudiesFemaleHumansMagnetic Resonance ImagingMaleNeuropsychological TestsPositron-Emission TomographyProdromal Symptomstau ProteinsAmyloid beta-Peptidestau ProteinsAmyloidConceptual discriminationPreclinical Alzheimer's diseaseRhinal cortexTau

Identifiers

PMID40897577
PMCPMC12501345

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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.