White matter microstructure in school-age children with down syndrome
- PMID: 40043413
- PMCID: PMC11928993
- DOI: 10.1016/j.dcn.2025.101540
White matter microstructure in school-age children with down syndrome
Abstract
Down syndrome (DS) is the most common genetic cause of intellectual disability, but our understanding of white matter microstructure in children with DS remains limited. Previous studies have reported reductions in white matter integrity, but nearly all studies to date have been conducted in adults or relied solely on diffusion tensor imaging (DTI), which lacks the ability to disentangle underlying properties of white matter organization. This study examined white matter microstructural differences in 7- to 12-year-old children with DS (n = 23), autism (n = 27), and typical development (n = 50) using DTI as well as High Angular Resolution Diffusion Imaging, and Neurite Orientation and Dispersion Imaging. There was a spatially specific pattern of results that showed a dissociation between intra- and inter-hemispheric pathways. Intra-hemispheric pathways (e.g., inferior fronto-occipital fasciculus, superior longitudinal fasciculus) exhibited reduced organization and structural integrity. Inter-hemispheric pathways (e.g., corpus callosum projections) and motor pathways (e.g., corticospinal tract) showed denser neurite packing and lower neurite dispersion. The current findings provide early insight into white matter development in school-aged children with DS and have the potential to further elucidate microstructural differences and inform more targeted clinical trials than what has previously been observed through DTI models alone.
Keywords: Axonal density; Diffusion imaging; Down syndrome; Fiber pathways; Neurite dispersion; White matter development.
Published by Elsevier Ltd.
Conflict of interest statement
Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Robert C. McKinstry reports a relationship with Turing Medical that includes: board membership and consulting or advisory. Robert C. McKinstry reports a relationship with Siemens Healthcare that includes: speaking and lecture fees and travel reimbursement. If there are other authors, they declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
Figures



Similar articles
-
White matter correlates of language ability in chinese boys with autism spectrum disorder: a diffusional kurtosis imaging study.Eur J Pediatr. 2025 Jul 14;184(8):480. doi: 10.1007/s00431-025-06325-z. Eur J Pediatr. 2025. PMID: 40658215
-
Elucidating Microstructural Alterations in Neurodevelopmental Disorders: Application of Advanced Diffusion-Weighted Imaging in Children With Rasopathies.Hum Brain Mapp. 2024 Dec 1;45(17):e70087. doi: 10.1002/hbm.70087. Hum Brain Mapp. 2024. PMID: 39665502 Free PMC article.
-
White-matter tract abnormalities and antisocial behavior: A systematic review of diffusion tensor imaging studies across development.Neuroimage Clin. 2017 Jan 16;14:201-215. doi: 10.1016/j.nicl.2017.01.014. eCollection 2017. Neuroimage Clin. 2017. PMID: 28180079 Free PMC article.
-
Longitudinal diffusion tensor imaging correlates with amyloid burden in Down syndrome.Alzheimers Dement. 2025 Aug;21(8):e70572. doi: 10.1002/alz.70572. Alzheimers Dement. 2025. PMID: 40779433 Free PMC article.
-
Alteration of fractional anisotropy in preterm-born individuals: a systematic review and meta-analysis.J Obstet Gynaecol. 2024 Dec;44(1):2371956. doi: 10.1080/01443615.2024.2371956. Epub 2024 Jul 10. J Obstet Gynaecol. 2024. PMID: 38984803
Cited by
-
Early White Matter Microstructure Alterations in Infants with Down Syndrome.medRxiv [Preprint]. 2025 Feb 27:2025.02.26.25322913. doi: 10.1101/2025.02.26.25322913. medRxiv. 2025. PMID: 40061339 Free PMC article. Preprint.
References
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
Medical