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Long‐term white matter tract reorganization following prolonged febrile seizures

OBJECTIVE: Diffusion magnetic resonance imaging (MRI) studies have demonstrated acute white matter changes following prolonged febrile seizures (PFS), but their longer‐term evolution is unknown. We investigated a population‐based cohort to determine white matter diffusion properties 8 years after PF...

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Autores principales: Pujar, Suresh S., Seunarine, Kiran K., Martinos, Marina M., Neville, Brian G. R., Scott, Rod C., Chin, Richard F. M., Clark, Chris A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5484997/
https://www.ncbi.nlm.nih.gov/pubmed/28332711
http://dx.doi.org/10.1111/epi.13724
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author Pujar, Suresh S.
Seunarine, Kiran K.
Martinos, Marina M.
Neville, Brian G. R.
Scott, Rod C.
Chin, Richard F. M.
Clark, Chris A.
author_facet Pujar, Suresh S.
Seunarine, Kiran K.
Martinos, Marina M.
Neville, Brian G. R.
Scott, Rod C.
Chin, Richard F. M.
Clark, Chris A.
author_sort Pujar, Suresh S.
collection PubMed
description OBJECTIVE: Diffusion magnetic resonance imaging (MRI) studies have demonstrated acute white matter changes following prolonged febrile seizures (PFS), but their longer‐term evolution is unknown. We investigated a population‐based cohort to determine white matter diffusion properties 8 years after PFS. METHODS: We used diffusion tensor imaging (DTI) and applied Tract‐Based Spatial Statistics for voxel‐wise comparison of white matter microstructure between 26 children with PFS and 27 age‐matched healthy controls. Age, gender, handedness, and hippocampal volumes were entered as covariates for voxel‐wise analysis. RESULTS: Mean duration between the episode of PFS and follow‐up was 8.2 years (range 6.7–9.6). All children were neurologically normal, and had normal conventional neuroimaging. On voxel‐wise analysis, compared to controls, the PFS group had (1) increased fractional anisotropy in early maturing central white matter tracts, (2) increased mean and axial diffusivity in several peripheral white matter tracts and late‐maturing central white matter tracts, and (3) increased radial diffusivity in peripheral white matter tracts. None of the tracts had reduced fractional anisotropy or diffusivity indices in the PFS group. SIGNIFICANCE: In this homogeneous, population‐based sample, we found increased fractional anisotropy in early maturing central white matter tracts and increased mean and axial diffusivity with/without increased radial diffusivity in several late‐maturing peripheral white matter tracts 8 years post‐PFS. We propose disruption in white matter maturation secondary to seizure‐induced axonal injury, with subsequent neuroplasticity and microstructural reorganization as a plausible explanation.
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spelling pubmed-54849972017-07-10 Long‐term white matter tract reorganization following prolonged febrile seizures Pujar, Suresh S. Seunarine, Kiran K. Martinos, Marina M. Neville, Brian G. R. Scott, Rod C. Chin, Richard F. M. Clark, Chris A. Epilepsia Full‐length Original Research OBJECTIVE: Diffusion magnetic resonance imaging (MRI) studies have demonstrated acute white matter changes following prolonged febrile seizures (PFS), but their longer‐term evolution is unknown. We investigated a population‐based cohort to determine white matter diffusion properties 8 years after PFS. METHODS: We used diffusion tensor imaging (DTI) and applied Tract‐Based Spatial Statistics for voxel‐wise comparison of white matter microstructure between 26 children with PFS and 27 age‐matched healthy controls. Age, gender, handedness, and hippocampal volumes were entered as covariates for voxel‐wise analysis. RESULTS: Mean duration between the episode of PFS and follow‐up was 8.2 years (range 6.7–9.6). All children were neurologically normal, and had normal conventional neuroimaging. On voxel‐wise analysis, compared to controls, the PFS group had (1) increased fractional anisotropy in early maturing central white matter tracts, (2) increased mean and axial diffusivity in several peripheral white matter tracts and late‐maturing central white matter tracts, and (3) increased radial diffusivity in peripheral white matter tracts. None of the tracts had reduced fractional anisotropy or diffusivity indices in the PFS group. SIGNIFICANCE: In this homogeneous, population‐based sample, we found increased fractional anisotropy in early maturing central white matter tracts and increased mean and axial diffusivity with/without increased radial diffusivity in several late‐maturing peripheral white matter tracts 8 years post‐PFS. We propose disruption in white matter maturation secondary to seizure‐induced axonal injury, with subsequent neuroplasticity and microstructural reorganization as a plausible explanation. John Wiley and Sons Inc. 2017-03-23 2017-05 /pmc/articles/PMC5484997/ /pubmed/28332711 http://dx.doi.org/10.1111/epi.13724 Text en © 2017 The Authors. Epilepsia published by Wiley Periodicals, Inc. on behalf of International League Against Epilepsy. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Full‐length Original Research
Pujar, Suresh S.
Seunarine, Kiran K.
Martinos, Marina M.
Neville, Brian G. R.
Scott, Rod C.
Chin, Richard F. M.
Clark, Chris A.
Long‐term white matter tract reorganization following prolonged febrile seizures
title Long‐term white matter tract reorganization following prolonged febrile seizures
title_full Long‐term white matter tract reorganization following prolonged febrile seizures
title_fullStr Long‐term white matter tract reorganization following prolonged febrile seizures
title_full_unstemmed Long‐term white matter tract reorganization following prolonged febrile seizures
title_short Long‐term white matter tract reorganization following prolonged febrile seizures
title_sort long‐term white matter tract reorganization following prolonged febrile seizures
topic Full‐length Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5484997/
https://www.ncbi.nlm.nih.gov/pubmed/28332711
http://dx.doi.org/10.1111/epi.13724
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