Literature DB >> 28370719

Brain structure and organization five decades after childhood onset epilepsy.

Camille Garcia-Ramos1,2, Sam Bobholz1, Kevin Dabbs1, Bruce Hermann1, Juho Joutsa3,4,5, Juha O Rinne3,4, Mira Karrasch6, Vivek Prabhakaran7, Shlomo Shinnar8, Matti Sillanpää9,10.   

Abstract

The purpose of this project was to characterize brain structure and organization in persons with active and remitted childhood onset epilepsy 50 years after diagnosis compared with healthy controls. Participants from a population-based investigation of uncomplicated childhood onset epilepsy were followed up 5 decades later. Forty-one participants had a history of childhood onset epilepsy (mean age of onset = 5.2 years, current chronological age = 56.0 years) and were compared with 48 population-based controls (mean age = 55.9 years). Of the epilepsy participants, 8 had persisting active epilepsy and in 33 the epilepsy had remitted. All participants underwent 3T MRI with subsequent vertex analysis of cortical volume, thickness, surface area and gyral complexity. In addition, cortical and subcortical volumes, including regions of the frontal, parietal, temporal, and occipital lobes, and subcortical structures including amygdala, thalamus, and hippocampus, were analyzed using graph theory techniques. There were modest group differences in traditional vertex-based analyses of cortical volume, thickness, surface area and gyral index, as well as across volumes of subcortical structures, after correction for multiple comparisons. Graph theory analyses revealed suboptimal topological structural organization with enhanced network segregation and reduced global integration in the epilepsy participants compared with controls, these patterns significantly more extreme in the active epilepsy group. Furthermore, both groups with epilepsy presented a greater number of higher Z-score regions in betweenness centrality (BC) than lower Z-score regions compared with controls. Also, contrary to the group with remitted epilepsy, patients with active epilepsy presented most of their high BC Z-score regions in subcortical areas including the amygdala, thalamus, hippocampus, pallidum, and accumbens. Overall, this population-based investigation of long term outcome (5 decades) of childhood onset epilepsy reveals persisting abnormalities, especially when examined by graph theoretical measurements, and provides new insights into the very long-term outcomes of active and remitted epilepsy. Hum Brain Mapp 38:3289-3299, 2017.
© 2017 Wiley Periodicals, Inc. © 2017 Wiley Periodicals, Inc.

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Keywords:  MRI; brain development; epilepsy; graph theory

Mesh:

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Year:  2017        PMID: 28370719      PMCID: PMC5479770          DOI: 10.1002/hbm.23593

Source DB:  PubMed          Journal:  Hum Brain Mapp        ISSN: 1065-9471            Impact factor:   5.038


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  2 in total

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Authors:  Bruce Hermann; Lisa L Conant; Cole J Cook; Gyujoon Hwang; Camille Garcia-Ramos; Kevin Dabbs; Veena A Nair; Jedidiah Mathis; Charlene N Rivera Bonet; Linda Allen; Dace N Almane; Karina Arkush; Rasmus Birn; Edgar A DeYoe; Elizabeth Felton; Rama Maganti; Andrew Nencka; Manoj Raghavan; Umang Shah; Veronica N Sosa; Aaron F Struck; Candida Ustine; Anny Reyes; Erik Kaestner; Carrie McDonald; Vivek Prabhakaran; Jeffrey R Binder; Mary E Meyerand
Journal:  Neuroimage Clin       Date:  2020-07-10       Impact factor: 4.881

2.  A Purinergic P2 Receptor Family-Mediated Increase in Thrombospondin-1 Bolsters Synaptic Density and Epileptic Seizure Activity in the Amygdala-Kindling Rat Model.

Authors:  Hongliu Sun; Luyu Ma; Yurong Zhang; Xiaohong Pan; Chaoyun Wang; Jinjin Zhang; Xiuli Zhang; Hongwei Sun; Qiaoyun Wang; Wei Zhu
Journal:  Front Cell Neurosci       Date:  2018-10-01       Impact factor: 5.505

  2 in total

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