Altered resting-state connectivity during interictal generalized spike-wave discharges in drug-naïve childhood absence epilepsy.

Abstract:

PURPOSE:To investigate the intrinsic brain connections at the time of interictal generalized spike-wave discharges (GSWDs) to understand their mechanism of effect on brain function in untreated childhood absence epilepsy (CAE). METHODS:The EEG-functional MRI (fMRI) was used to measure the resting state functional connectivity during interictal GSWDs in drug-naïve CAE, and three different brain networks-the default mode network (DMN), cognitive control network (CCN), and affective network (AN)-were investigated. RESULTS:Cross-correlation functional connectivity analysis with priori seed revealed decreased functional connectivity within each of these three networks in the CAE patients during interictal GSWDS. It included precuneus-dorsolateral prefrontal cortex (DLPFC), dorsomedial prefrontal cortex (DMPFC), and inferior parietal lobule in the DMN; DLPFC-inferior frontal junction (IFJ), and pre-supplementary motor area (pre-SMA) subregions connectivity disruption in CCN; ACC-ventrolateral prefrontal cortex (VLPFC) and DMPFC in AN; There were also some regions, primarily the parahippcampus, paracentral in AN, and the left frontal mid orb in the CCN, which showed increased connectivity. CONCLUSIONS:The current findings demonstrate significant alterations of resting-state networks in drug naïve CAE subjects during interictal GSWDs and interictal GSWDs can cause dysfunction in specific networks important for psychosocial function. Impairment of these networks may cause deficits both during and between seizures. Our study may contribute to the understanding of neuro-pathophysiological mechanism of psychosocial function impairments in patients with CAE.

journal_name

Hum Brain Mapp

journal_title

Human brain mapping

authors

Yang T,Luo C,Li Q,Guo Z,Liu L,Gong Q,Yao D,Zhou D

doi

10.1002/hbm.22025

subject

Has Abstract

pub_date

2013-08-01 00:00:00

pages

1761-7

issue

8

eissn

1065-9471

issn

1097-0193

journal_volume

34

pub_type

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