Literature DB >> 16180210

Negative BOLD responses to epileptic spikes.

Eliane Kobayashi1, Andrew P Bagshaw, Christophe Grova, François Dubeau, Jean Gotman.   

Abstract

Simultaneous electroencephalogram/functional magnetic resonance imaging (EEG-fMRI) during interictal epileptiform discharges can result in positive (activation) and negative (deactivation) changes in the blood oxygenation level-dependent (BOLD) signal. Activation probably reflects increased neuronal activity and energy demand, but deactivation is more difficult to explain. Our objective was to evaluate the occurrence and significance of deactivations related to epileptiform discharges in epilepsy. We reviewed all EEG-fMRI studies from our database, identified those with robust responses (P = 0.01, with > or =5 contiguous voxels with a |t| > 3.1, including > or =1 voxel at |t| > 5.0), and divided them into three groups: activation (A = 8), deactivation (D = 9), and both responses (AD = 43). We correlated responses with discharge type and location and evaluated their spatial relationship with regions involved in the "default" brain state (Raichle et al. [2001]: Proc Natl Acad Sci 98:676-682]. Deactivations were seen in 52/60 studies (AD + D): 26 related to focal discharges, 12 bilateral, and 14 generalized. Deactivations were usually distant from anatomical areas related to the discharges and more frequently related to polyspike- and spike-and-slow waves than to spikes. The "default" pattern occurred in 10/43 AD studies, often associated with bursts of generalized discharges. In conclusion, deactivations are frequent, mostly with concomitant activation, for focal and generalized discharges. Discharges followed by a slow wave are more likely to result in deactivation, suggesting neuronal inhibition as the underlying phenomenon. Involvement of the "default" areas, related to bursts of generalized discharges, provides evidence of a subclinical effect of the discharges, temporarily suspending normal brain function in the resting state. Copyright 2005 Wiley-Liss, Inc.

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Year:  2006        PMID: 16180210      PMCID: PMC6871405          DOI: 10.1002/hbm.20193

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


  31 in total

1.  A default mode of brain function.

Authors:  M E Raichle; A M MacLeod; A Z Snyder; W J Powers; D A Gusnard; G L Shulman
Journal:  Proc Natl Acad Sci U S A       Date:  2001-01-16       Impact factor: 11.205

2.  Reduction of excitability ("inhibition") in the ipsilateral primary motor cortex is mirrored by fMRI signal decreases.

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3.  Reciprocal modulation and attenuation in the prefrontal cortex: an fMRI study on emotional-cognitive interaction.

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4.  Cortical functional architecture and local coupling between neuronal activity and the microcirculation revealed by in vivo high-resolution optical imaging of intrinsic signals.

Authors:  R D Frostig; E E Lieke; D Y Ts'o; A Grinvald
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5.  Intrinsic epileptogenicity in polymicrogyric cortex suggested by EEG-fMRI BOLD responses.

Authors:  E Kobayashi; A P Bagshaw; A Jansen; F Andermann; E Andermann; J Gotman; F Dubeau
Journal:  Neurology       Date:  2005-04-12       Impact factor: 9.910

6.  Spatio-temporal imaging of focal interictal epileptiform activity using EEG-triggered functional MRI.

Authors:  K Krakow; L Lemieux; D Messina; C A Scott; M R Symms; J S Duncan; D R Fish
Journal:  Epileptic Disord       Date:  2001-06       Impact factor: 1.819

7.  The BOLD response to interictal epileptiform discharges.

Authors:  Christian G Bénar; Donald W Gross; Yunhua Wang; Valentina Petre; Bruce Pike; François Dubeau; Jean Gotman
Journal:  Neuroimage       Date:  2002-11       Impact factor: 6.556

8.  Analysis of the EEG-fMRI response to prolonged bursts of interictal epileptiform activity.

Authors:  Andrew P Bagshaw; Colin Hawco; Christian-G Bénar; Eliane Kobayashi; Yahya Aghakhani; François Dubeau; G Bruce Pike; Jean Gotman
Journal:  Neuroimage       Date:  2004-12-01       Impact factor: 6.556

Review 9.  Searching for a baseline: functional imaging and the resting human brain.

Authors:  D A Gusnard; M E Raichle; M E Raichle
Journal:  Nat Rev Neurosci       Date:  2001-10       Impact factor: 34.870

10.  Hemodynamic and metabolic responses to neuronal inhibition.

Authors:  Bojana Stefanovic; Jan M Warnking; G Bruce Pike
Journal:  Neuroimage       Date:  2004-06       Impact factor: 6.556

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  60 in total

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Journal:  Hum Brain Mapp       Date:  2015-04-16       Impact factor: 5.038

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4.  ICA decomposition of EEG signal for fMRI processing in epilepsy.

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Review 5.  Endogenous brain oscillations and related networks detected by surface EEG-combined fMRI.

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Journal:  Hum Brain Mapp       Date:  2008-07       Impact factor: 5.038

6.  Localization of focal epileptic discharges using functional connectivity magnetic resonance imaging.

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Journal:  J Neurosurg       Date:  2011-02-25       Impact factor: 5.115

7.  EEG-fMRI: adding to standard evaluations of patients with nonlesional frontal lobe epilepsy.

Authors:  F Moeller; L Tyvaert; D K Nguyen; P LeVan; A Bouthillier; E Kobayashi; D Tampieri; F Dubeau; J Gotman
Journal:  Neurology       Date:  2009-12-08       Impact factor: 9.910

8.  The neural correlates of volitional attention: A combined fMRI and ERP study.

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Journal:  Hum Brain Mapp       Date:  2015-03-02       Impact factor: 5.038

9.  Different structures involved during ictal and interictal epileptic activity in malformations of cortical development: an EEG-fMRI study.

Authors:  L Tyvaert; C Hawco; E Kobayashi; P LeVan; F Dubeau; J Gotman
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10.  The spatio-temporal mapping of epileptic networks: combination of EEG-fMRI and EEG source imaging.

Authors:  S Vulliemoz; R Thornton; R Rodionov; D W Carmichael; M Guye; S Lhatoo; A W McEvoy; L Spinelli; C M Michel; J S Duncan; L Lemieux
Journal:  Neuroimage       Date:  2009-07-01       Impact factor: 6.556

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