RT Journal Article
SR Electronic
T1 Developmental neuroplasticity of the white matter connectome in children with perinatal stroke
JF Neurology
JO Neurology
FD Lippincott Williams & Wilkins
SP e2476
OP e2486
DO 10.1212/WNL.0000000000010669
VO 95
IS 18
A1 Craig, Brandon T.
A1 Hilderley, Alicia
A1 Kinney-Lang, Eli
A1 Long, Xiangyu
A1 Carlson, Helen L.
A1 Kirton, Adam
YR 2020
UL http://n.neurology.org/content/95/18/e2476.abstract
AB Objective To employ diffusion imaging connectome methods to explore network development in the contralesional hemisphere of children with perinatal stroke and its relationship to clinical function. We hypothesized alterations in global efficiency of the intact hemisphere would correlate with clinical disability.Methods Children with unilateral perinatal arterial (n = 26) or venous (n = 27) stroke and typically developing controls (n = 32) underwent 3T diffusion and T1 anatomical MRI and completed established motor assessments. A validated atlas coregistered to whole-brain tractography for each individual was used to estimate connectivity between 47 regions. Graph theory metrics (assortativity, hierarchical coefficient of regression, global and local efficiency, and small worldness) were calculated for the left hemisphere of controls and the intact contralesioned hemisphere of both stroke groups. Validated clinical motor assessments were then correlated with connectivity outcomes.Results Global efficiency was higher in arterial strokes compared to venous strokes (p < 0.001) and controls (p < 0.001) and was inversely associated with all motor assessments (all p < 0.012). Additional graph theory metrics including assortativity, hierarchical coefficient of regression, and local efficiency also demonstrated consistent differences in the intact hemisphere associated with clinical function.Conclusions The structural connectome of the contralesional hemisphere is altered after perinatal stroke and correlates with clinical function. Connectomics represents a powerful tool to understand whole brain developmental plasticity in children with disease-specific cerebral palsy.AAL2=automated anatomic labeling 2; ACT=anatomically constrained tractography; AHA=Assisting Hand Assessment; AIS=arterial ischemic stroke; BBTA=Box and Block Test, affected; BBTU=Box and Block Test, unaffected; CI=confidence interval; CSD=constrained spherical deconvolution; CST=corticospinal tract; dMRI=diffusion MRI; FSL=FMRIB Software Library; GM=gray matter; GRETNA=graph-theoretical network analysis toolbox; HCP=hemiparetic cerebral palsy; HCR=hierarchical coefficient of regression; JTHFA=Jebsen Taylor Hand Function, affected; JTHFU=Jebsen Taylor Hand Function, unaffected; MUUL=Melbourne Assessment of Unilateral Upper Limb Function; PVI=periventricular venous infarction; TDC=typically developing control; TE=echo time; TR=repetition time; WM=white matter