Evidence map›Paper›PMID 40170168›Full record

ArticleJournal of neurodevelopmental disorders2025

Brain structure in triple X syndrome: regional gray matter volume and cortical thickness in adult women with 47,XXX karyotype.

Gregor Domes, Marie-Anne Croyé, Petra Freilinger, Andreas Bohlscheid, Winfried A Willinek, Jobst Meyer

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Article in Journal of neurodevelopmental disorders, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

What it found

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Gregor DomesDepartment of Biological and Clinical Psychology, University of Trier, Johanniterufer 15, 54290, Trier, Germany. domes@uni-trier.de.
Marie-Anne CroyéDepartment of Neurobehavioral Genetics, University of Trier, Trier, Germany.
Petra FreilingerGenetikum, Neu-Ulm, Germany.
Andreas BohlscheidDepartment of Radiology, Neuroradiology, Sonography and Nuclear Medicine, Hospital of the Barmherzige Brüder Trier, Trier, Germany.
Winfried A WillinekDepartment of Radiology, Neuroradiology, Sonography and Nuclear Medicine, Hospital of the Barmherzige Brüder Trier, Trier, Germany.
Jobst MeyerInstitute for Cognitive and Affective Neuroscience, University of Trier, Trier, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChanges in the brain structure of women with Triple X syndrome (karyotype 47,XXX) have been described in a few studies to date, including reduced total brain volume and regional reductions in gray substance in cortical and subcortical areas. However, the empirical evidence from adults is very limited and group comparison on a voxel-wise basis for gray matter volume and cortical thickness is still missing.

methodsUsing voxel-based morphometry (VBM) and surface-based morphometry (SBM), we investigated regional gray matter changes in a sample of n = 20 adult women (aged 18-49 years) with 47,XXX karyotype using T1-weighted 3T MRI scans.

resultsCompared to an age- and education-matched control group (and controlled for differences in total intracranial volume), the VBM revealed decreased regional gray matter volumes in the hippocampus, amygdala, parts of the basal ganglia, insula, prefrontal areas and cerebellum. To a lesser extent, we also noted specific reductions in cortical thickness in a smaller part of those regions.

conclusionThe observed network is significantly involved in the processing of cognitive, affective, and social stimuli and might be a potential neuronal correlate of the autism-like social-cognitive problems described in 47,XXX in the literature.

Indexed as

BrainCerebral CortexGray MatterSex Chromosome DisordersSex Chromosome Disorders of Sex DevelopmentTrisomyAdolescentAdultChromosomes, Human, XFemaleHumansMagnetic Resonance ImagingMiddle AgedOrgan SizeSex Chromosome AberrationsYoung Adult47,XXXAmygdalaBasal gangliaCerebellumHippocampusMagnetic resonance imagingMorphometryTriple X syndromeTrisomy X

Identifiers

PMID40170168
PMCPMC11959852

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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.