Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/12393
Full metadata record
DC FieldValueLanguage
dc.contributor.authorCarney, Patrick Wen
dc.contributor.authorJackson, Graeme Den
dc.date.accessioned2015-05-16T02:05:14Z
dc.date.available2015-05-16T02:05:14Z
dc.date.issued2014-09-01en
dc.identifier.citationFrontiers in Neurology 2014; 5(): 162en
dc.identifier.govdoc25225491en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/12393en
dc.description.abstractAbsence seizures (AS) are brief epileptic events characterized by loss of awareness with subtle motor features. They may be very frequent, and impact on attention, learning, and memory. A number of pathophysiological models have been developed to explain the mechanism of absence seizure generation, which relies heavily on observations from animal studies. Studying the structural and functional relationships between large-scale brain networks in humans is only practical with non-invasive whole brain techniques. EEG with functional MRI (EEG-fMRI) is one such technique that provides an opportunity to explore the interactions between brain structures involved in AS generation. A number of fMRI techniques including event-related analysis, time-course analysis, and functional connectivity (FC) have identified a common network of structures involved in AS. This network comprises the thalamus, midline, and lateral parietal cortex [the default mode network (DMN)], caudate nuclei, and the reticular structures of the pons. The main component displaying an increase in blood oxygen level dependent (BOLD) signal relative to the resting state, in group studies, is the thalamus while the most consistent cortical change is reduced BOLD signal in the DMN. Time-course analysis shows that, rather than some structures being activated or inactivated during AS, there appears to be increase in activity across components of the network preceding or following the electro-clinical onset of the seizure. The earliest change in BOLD signal occurs in the DMN, prior to the onset of epileptiform events. This region also shows altered FC in patients with AS. Hence, it appears that engagement of this network is central to AS. In this review, we will explore the insights of EEG-fMRI studies into the mechanisms of AS and consider how the DMN is likely to be the major large-scale brain network central to both seizure generation and seizure manifestations.en
dc.language.isoenen
dc.subject.otherabsence seizuresen
dc.subject.otherdefault mode networken
dc.subject.otherepilepsyen
dc.subject.otherfunctional MRIen
dc.subject.otherfunctional connectivityen
dc.titleInsights into the mechanisms of absence seizure generation provided by EEG with functional MRI.en
dc.typeJournal Articleen
dc.identifier.journaltitleFrontiers in neurologyen
dc.identifier.affiliationThe Florey Institute for Neuroscience and Mental Health , Heidelberg, VIC , Australia ; The University of Melbourne , Parkville, VIC , Australia ; Austin Health , Heidelberg, VIC , Australiaen
dc.identifier.doi10.3389/fneur.2014.00162en
dc.description.pages162en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/25225491en
dc.type.austinJournal Articleen
local.name.researcherCarney, Patrick W
item.languageiso639-1en-
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.cerifentitytypePublications-
crisitem.author.deptNeurology-
crisitem.author.deptNeurology-
crisitem.author.deptThe Florey Institute of Neuroscience and Mental Health-
Appears in Collections:Journal articles
Show simple item record

Page view(s)

48
checked on Nov 7, 2024

Google ScholarTM

Check


Items in AHRO are protected by copyright, with all rights reserved, unless otherwise indicated.