Evidence map›Paper›PMID 42488757›Full record

ArticleBrain communications2026

Distinct brain regions are affected by neurodevelopmental or pre-dementia changes in Down syndrome.

Lília Jorge, Joana Oliveira, Ricardo Martins, Tânia Lopes, Hugo Quental, Miguel Castelo-Branco

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

6 authors.

Lília JorgeInstitute for Nuclear Sciences Applied to Health, University of Coimbra, 3000-548 Coimbra, Portugal.
Joana OliveiraInstitute for Nuclear Sciences Applied to Health, University of Coimbra, 3000-548 Coimbra, Portugal.
Ricardo MartinsInstitute for Nuclear Sciences Applied to Health, University of Coimbra, 3000-548 Coimbra, Portugal.ORCID https://orcid.org/0000-0001-7184-185X
Tânia LopesInstitute for Nuclear Sciences Applied to Health, University of Coimbra, 3000-548 Coimbra, Portugal.
Hugo QuentalInstitute for Nuclear Sciences Applied to Health, University of Coimbra, 3000-548 Coimbra, Portugal.
Miguel Castelo-BrancoInstitute for Nuclear Sciences Applied to Health, University of Coimbra, 3000-548 Coimbra, Portugal.ORCID https://orcid.org/0000-0003-4364-6373

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Down syndrome, a condition characterized by triplication of chromosome 21, leads to a complex interplay between neurodevelopmental and dementia-related changes similar to the ones observed in Alzheimer's disease. Here we aimed to understand this interplay by using imaging biomarkers for different cognitive profiles in Down syndrome, and by analysing early developmental differences versus age-related changes. We analysed voxel-based morphometric measures of grey matter volume from high-resolution T1-weighted MRI in 23 adults with Down syndrome (18-59 years, five female) in preclinical/prodromal stages of Alzheimer's disease and 24 age- and sex-matched controls, along with cognitive assessments. Neuroanatomical group differences were assessed using two-sample t-tests. Age-related effects on brain integrity, and cognitive function were examined through voxel-wise regression analyses and correlation tests, respectively. Finally, structural correlates of episodic memory were explored across the whole brain at the voxel level within the Down syndrome group. Results revealed a neuroanatomic phenotype with both regional increases and decreases in grey matter volume compared to controls (false discovery rate,

Indexed as

Alzheimer’s diseaseDown syndromeepisodic memoryneurodevelopmentstructural MRI

Identifiers

PMID42488757
PMCPMC13390646

What Socratic 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 Socratic graph.