Literature DB >> 26333833

Brain regions with abnormal network properties in severe epilepsy of Lennox-Gastaut phenotype: Multivariate analysis of task-free fMRI.

Mangor Pedersen1,2, Evan K Curwood2, John S Archer3,4, David F Abbott1,2, Graeme D Jackson1,2,3,4.   

Abstract

OBJECTIVE: Lennox-Gastaut syndrome, and the similar but less tightly defined Lennox-Gastaut phenotype, describe patients with severe epilepsy, generalized epileptic discharges, and variable intellectual disability. Our previous functional neuroimaging studies suggest that abnormal diffuse association network activity underlies the epileptic discharges of this clinical phenotype. Herein we use a data-driven multivariate approach to determine the spatial changes in local and global networks of patients with severe epilepsy of the Lennox-Gastaut phenotype.
METHODS: We studied 9 adult patients and 14 controls. In 20 min of task-free blood oxygen level-dependent functional magnetic resonance imaging data, two metrics of functional connectivity were studied: Regional homogeneity or local connectivity, a measure of concordance between each voxel to a focal cluster of adjacent voxels; and eigenvector centrality, a global connectivity estimate designed to detect important neural hubs. Multivariate pattern analysis of these data in a machine-learning framework was used to identify spatial features that classified disease subjects.
RESULTS: Multivariate pattern analysis was 95.7% accurate in classifying subjects for both local and global connectivity measures (22/23 subjects correctly classified). Maximal discriminating features were the following: increased local connectivity in frontoinsular and intraparietal areas; increased global connectivity in posterior association areas; decreased local connectivity in sensory (visual and auditory) and medial frontal cortices; and decreased global connectivity in the cingulate cortex, striatum, hippocampus, and pons. SIGNIFICANCE: Using a data-driven analysis method in task-free functional magnetic resonance imaging, we show increased connectivity in critical areas of association cortex and decreased connectivity in primary cortex. This supports previous findings of a critical role for these association cortical regions as a final common pathway in generating the Lennox-Gastaut phenotype. Abnormal function of these areas is likely to be important in explaining the intellectual problems characteristic of this disorder. Wiley Periodicals, Inc.
© 2015 International League Against Epilepsy.

Entities:  

Keywords:  Functional connectivity; Lennox-Gastaut syndrome; Multivariate pattern analysis; Secondary generalized epilepsy; fMRI

Mesh:

Year:  2015        PMID: 26333833     DOI: 10.1111/epi.13135

Source DB:  PubMed          Journal:  Epilepsia        ISSN: 0013-9580            Impact factor:   5.864


  4 in total

1.  Understanding Lennox-Gastaut syndrome: insights from focal epilepsy patients with Lennox-Gastaut features.

Authors:  Sophie Dupont; Raluca Banica-Wolters; Isabelle An-Gourfinkel; Virginie Lambrecq; Vincent Navarro; Claude Adam; Vi-Huong Nguyen-Michel
Journal:  J Neurol       Date:  2017-06-05       Impact factor: 4.849

Review 2.  A Hitchhiker's Guide to Functional Magnetic Resonance Imaging.

Authors:  José M Soares; Ricardo Magalhães; Pedro S Moreira; Alexandre Sousa; Edward Ganz; Adriana Sampaio; Victor Alves; Paulo Marques; Nuno Sousa
Journal:  Front Neurosci       Date:  2016-11-10       Impact factor: 4.677

3.  The dynamics of functional connectivity in neocortical focal epilepsy.

Authors:  Mangor Pedersen; Amir Omidvarnia; Evan K Curwood; Jennifer M Walz; Genevieve Rayner; Graeme D Jackson
Journal:  Neuroimage Clin       Date:  2017-04-11       Impact factor: 4.881

4.  Characteristics of Genetic Variations Associated With Lennox-Gastaut Syndrome in Korean Families.

Authors:  Jin Ok Yang; Min-Hyuk Choi; Ji-Yong Yoon; Jeong-Ju Lee; Sang Ook Nam; Soo Young Jun; Hyeok Hee Kwon; Sohyun Yun; Su-Jin Jeon; Iksu Byeon; Debasish Halder; Juhyun Kong; Byungwook Lee; Jeehun Lee; Joon-Won Kang; Nam-Soon Kim
Journal:  Front Genet       Date:  2021-01-20       Impact factor: 4.599

  4 in total

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