Evidence map›Paper›PMID 40506666›Full record

ArticleAlzheimer's & dementia : the journal of the Alzheimer's Association2025

White matter trajectories in Down syndrome and Alzheimer's disease: Insights from diffusion tensor-based morphometry.

Fedal Saini, Phoebe Ivain, Mina Idris, Jasmine Wells, Leda Bianchi, Miren Tamayo-Elizalde, Flavio Dell'Acqua, André Strydom

Abstract read
In one paragraph

Article in Alzheimer's & dementia : the journal of the Alzheimer's Association, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
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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

8 authors.

Fedal SainiInstitute of Psychiatry, Psychology & Neuroscience, Department of Forensic and Neurodevelopmental Sciences, King's College London, London, UK.ORCID 0000-0003-0104-1405
Phoebe IvainInstitute of Psychiatry, Psychology & Neuroscience, Department of Forensic and Neurodevelopmental Sciences, King's College London, London, UK.
Mina IdrisInstitute of Psychiatry, Psychology & Neuroscience, Department of Forensic and Neurodevelopmental Sciences, King's College London, London, UK.
Jasmine WellsOxford Institute of Clinical Psychology Training and Research, Isis Education Centre, Warneford Hospital, Oxford, UK.
Leda BianchiInstitute of Psychiatry, Psychology & Neuroscience, Department of Forensic and Neurodevelopmental Sciences, King's College London, London, UK.
Miren Tamayo-ElizaldeInstitute of Psychiatry, Psychology & Neuroscience, Department of Forensic and Neurodevelopmental Sciences, King's College London, London, UK.
Flavio Dell'AcquaInstitute of Psychiatry, Psychology & Neuroscience, Department of Forensic and Neurodevelopmental Sciences, King's College London, London, UK.
André StrydomInstitute of Psychiatry, Psychology & Neuroscience, Department of Forensic and Neurodevelopmental Sciences, King's College London, London, UK.

Funding

Fondation Jérôme Lejeune PDC-2024/85Medical Research Council MR/S011277/1
6 · The paper itself

Abstract

introductionDiffusion magnetic resonance imaging studies investigating Down syndrome (DS) and Alzheimer's disease (AD) have mainly relied on white matter (WM) skeleton-based techniques, potentially overlooking broader WM architecture.

methodWe applied diffusion tensor-based morphometry (D-TBM), a novel whole-volume WM registration technique, to characterize WM properties in DS. Between- and within-group analyses were conducted in 51 adults with DS and 35 controls, divided into two age groups, using diffusion tensor imaging (DTI)-derived metrics and local volumetric changes.

resultsDS participants exhibited extensive volumetric and DTI-based differences affecting association fibers and commissures. Within-group comparisons revealed further changes in older DS participants in these fibers. Reduced axial diffusivity (AxD) in temporal and commissural WM was reported for the first time in DS. DISCUSSION: DTI changes in the older DS cohort affect WM structures supporting language, memory, and executive functions and may be due to AD-related atrophy. Reduced AxD may reflect neuroinflammation or atypical WM development. HIGHLIGHTS: Diffusion tensor-based morphometry (D-TBM) was applied for the first time in Down syndrome (DS) adults. Diffusion tensor imaging alterations in DS affect structures for language, memory, and executive functions. Increased radial diffusivity and mean diffusivity in older DS adults highlight Alzheimer's disease (AD)-related neurodegeneration in key tracts. AD in DS affects commissural structures, including the genu of the corpus callosum. Axial diffusivity reductions in DS may indicate neuroinflammation.

Indexed as

Alzheimer DiseaseBrainDiffusion Tensor ImagingDown SyndromeWhite MatterAdultAgedFemaleHumansImage Processing, Computer-AssistedMaleMiddle AgedAlzheimer's diseasedementiadiffusion magnetic resonance imagingdiffusion tensor–based morphometrydiffusion tensor imagingDown syndromeneurodegenerationstructural connectivitytrisomy 21white matter

Identifiers

PMID40506666
PMCPMC12162262

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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.