In:
Human Brain Mapping, Wiley, Vol. 40, No. 17 ( 2019-12), p. 4888-4900
Abstract:
Children with unilateral cerebral palsy (UCP) due to early brain injury exhibit disrupted connectivity of corticospinal tracts (CSTs), which can be quantified using diffusion‐weighted magnetic resonance imaging (DWI). Diffusion tensor imaging (DTI) is commonly used to quantify white matter organization, however, this model lacks the biological specificity to accurately describe underlying microstructural properties. Newer approaches, such as neurite orientation dispersion and density imaging (NODDI), may provide more biologically accurate information regarding CST microstructure. In this study, we directly compared metrics of CST microstructure using NODDI and DTI models to characterize the microstructural organization of corticospinal pathways. Twenty participants with UCP participating in a neuromodulation/rehabilitation intervention underwent imaging including multi‐shell DWI; 10 participants' datasets were adequately completed for neuroimaging analysis. Task fMRI‐guided probabilistic tractography from motor cortex to brainstem was performed at baseline and follow‐up to reconstruct the CSTs. Diffusion metrics were compared between hemispheres at baseline, and between baseline and follow‐up to test for intervention effects. Correlation analyses were used to compare baseline metrics to changes in hand function following the intervention. DTI results showed that mean fractional anisotropy in lesioned and nonlesioned CSTs did not significantly differ, but mean, axial, and radial diffusivity were greater in the lesioned CST. For NODDI, intracellular volume fraction (ICVF) and orientation dispersion index (ODI) were lower in the lesioned CST. Unimanual function was strongly correlated with ICVF, but not FA. NODDI may reveal distinct properties of CST microstructure that are linked to motor function, indicating their potential in characterizing brain structure and development.
Type of Medium:
Online Resource
ISSN:
1065-9471
,
1097-0193
Language:
English
Publisher:
Wiley
Publication Date:
2019
detail.hit.zdb_id:
1492703-2
