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Fronto‐temporal vulnerability to disconnection in paediatric moderate and severe traumatic brain injury
Author(s) -
Molteni E.,
Pagani E.,
Strazzer S.,
Arrigoni F.,
Beretta E.,
Boffa G.,
Galbiati S.,
Filippi M.,
Rocca M. A.
Publication year - 2019
Publication title -
european journal of neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.881
H-Index - 124
eISSN - 1468-1331
pISSN - 1351-5101
DOI - 10.1111/ene.13963
Subject(s) - medicine , atrophy , white matter , uncinate fasciculus , corpus callosum , fasciculus , frontal lobe , diffusion mri , magnetic resonance imaging , cardiology , pathology , fractional anisotropy , radiology , psychiatry
Background In patients with moderate and severe paediatric traumatic brain injury (TBI), we investigated the presence and severity of white matter (WM) tract damage, cortical lobar and deep grey matter (GM) atrophies, their interplay and their correlation with outcome rating scales. Methods Diffusion tensor (DT) and 3D T1‐weighted MRI scans were obtained from 22 TBI children (13 boys; mean age at insult = 11.6 years; 72.7% in chronic condition) and 31 age‐matched healthy children. Patients were tested with outcome rating scales and the Wechsler Intelligence Scale for Children (WISC). DT MRI indices were obtained from several supra‐ and infra‐tentorial WM tracts. Cortical lobar and deep GM volumes were derived. Comparisons between patients and controls, and between patients in acute (<6 months from the event) vs. chronic (≥6 months) condition were performed. Results Patients showed a widespread pattern of decreased WM FA and GM atrophy. Compared to acute, chronic patients showed severer atrophy in the right frontal lobe and reduced FA in the left inferior longitudinal fasciculus and corpus callosum (CC). Decreased axial diffusivity was observed in acute patients versus controls in the inferior fronto‐occipital fasciculus and CC. Chronic patients showed increased axial diffusivity in the same structures. Uncinate fasciculus DT MRI abnormalities correlated with atrophy in the frontal and temporal lobes. Hippocampal atrophy correlated with reduced WISC scores, whereas putamen atrophy correlated with lower functional independence measure scores. Conclusions The study isolated a distributed fronto‐temporal network of structures particularly vulnerable to axonal damage and atrophy that may contribute to cognitive deficits following TBI.