4.8 Article

Quantitative MRI reveals differences in striatal myelin in children with DLD

期刊

ELIFE
卷 11, 期 -, 页码 -

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eLIFE SCIENCES PUBL LTD
DOI: 10.7554/eLife.74242

关键词

qMRI; microstructure; language impairment; children; caudate nucleus; speech motor; neurodevelopmental disorder; SLI; histological MRI; Human

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资金

  1. Medical Research Council
  2. NIHR Oxford Health Biomedical Research Centre
  3. Wellcome Trust
  4. [MR/P024149/1]
  5. [203139/Z/16/Z]

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This study used a novel imaging protocol to investigate microstructural neural differences in children with DLD, revealing lower MTsat values in certain brain regions and globally lower R1 values in DLD children, suggesting the presence of microstructural abnormalities.
authors Abstract Developmental language disorder (DLD) is a common neurodevelopmental disorder characterised by receptive or expressive language difficulties or both. While theoretical frameworks and empirical studies support the idea that there may be neural correlates of DLD in frontostriatal loops, findings are inconsistent across studies. Here, we use a novel semiquantitative imaging protocol - multi-parameter mapping (MPM) - to investigate microstructural neural differences in children with DLD. The MPM protocol allows us to reproducibly map specific indices of tissue micro-structure. In 56 typically developing children and 33 children with DLD, we derived maps of (1) longitudinal relaxation rate R1 (1/T1), (2) transverse relaxation rate R2* (1/T2*), and (3) Magnetization Transfer saturation (MTsat). R1 and MTsat predominantly index myelin, while R2* is sensitive to iron content. Children with DLD showed reductions in MTsat values in the caudate nucleus bilaterally, as well as in the left ventral sensorimotor cortex and Heschl & scaron; gyrus. They also had globally lower R1 values. No group differences were noted in R2* maps. Differences in MTsat and R1 were coincident in the caudate nucleus bilaterally. These findings support our hypothesis of corticostriatal abnormali-ties in DLD and indicate abnormal levels of myelin in the dorsal striatum in children with DLD.

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