AUTHOR=Papadelis Christos , Kaye Harper , Shore Benjamin , Snyder Brian , Grant Patricia Ellen , Rotenberg Alexander TITLE=Maturation of Corticospinal Tracts in Children With Hemiplegic Cerebral Palsy Assessed by Diffusion Tensor Imaging and Transcranial Magnetic Stimulation JOURNAL=Frontiers in Human Neuroscience VOLUME=Volume 13 - 2019 YEAR=2019 URL=https://www.frontiersin.org/journals/human-neuroscience/articles/10.3389/fnhum.2019.00254 DOI=10.3389/fnhum.2019.00254 ISSN=1662-5161 ABSTRACT=Aim: To assess changes in the developmental trajectory of corticospinal tracts maturation in children with hemiplegic cerebral palsy (HCP). Methods: Neuroimaging data were obtained from 36 children with HCP for both the more affected and less affected hemispheres, and, for purposes of direct comparison, between groups, 15 typically developing children. With diffusion tensor imaging, we estimated the mean fractional anisotropy, axial diffusivity, mean diffusivity, and radial diffusivity of the corticospinal tract, parameters indicative of factors including myelination and axon density. Transcranial magnetic stimulation (TMS) was performed as a neurophysiologic measure of corticospinal tract integrity and organization. Resting motor threshold was obtained per hemisphere, per patient. Results: We observed a significant axial diffusivity and mean diffusivity developmental trajectory, both of which were inversely related to age (decrease in axial diffusivity and diffusivity corresponding to increased age) in both hemispheres of typically developing children (p<0.001). This maturation process was absent in both more affected and less affected hemispheres of children with HCP. Additionally, the TMS-derived previously established resting motor threshold developmental trajectory was preserved in the less affected hemisphere of children with HCP (n=26; p<0.0001) but this trajectory was absent in the more affected hemisphere. Conclusions: Corticospinal tract maturation arrests in both hemispheres of children with hemiplegic cerebral palsy, possibly reflecting perinatal disruption of corticospinal tract myelination and axonal integrity.