Show simple item record

dc.contributor.authorAbela, E
dc.contributor.authorPawley, AD
dc.contributor.authorTangwiriyasakul, C
dc.contributor.authorYaakub, Siti Nurbaya
dc.contributor.authorChowdhury, FA
dc.contributor.authorElwes, RDC
dc.contributor.authorBrunnhuber, F
dc.contributor.authorRichardson, MP
dc.date.accessioned2023-02-20T14:56:00Z
dc.date.issued2018-12-18
dc.identifier.issn2328-9503
dc.identifier.issn2328-9503
dc.identifier.urihttp://hdl.handle.net/10026.1/20480
dc.description.abstract

<jats:title>Abstract</jats:title><jats:sec><jats:title>Objective</jats:title><jats:p>Slowing and frontal spread of the alpha rhythm have been reported in multiple epilepsy syndromes. We investigated whether these phenomena are associated with seizure control.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>We prospectively acquired resting‐state electroencephalogram (<jats:styled-content style="fixed-case">EEG</jats:styled-content>) in 63 patients with focal and idiopathic generalized epilepsy (<jats:styled-content style="fixed-case">FE</jats:styled-content> and <jats:styled-content style="fixed-case">IGE</jats:styled-content>) and 39 age‐ and gender‐matched healthy subjects (HS). Patients were divided into good and poor (≥4 seizures/12 months) seizure control groups based on self‐reports and clinical records. We computed spectral power from 20‐sec <jats:styled-content style="fixed-case">EEG</jats:styled-content> segments during eyes‐closed wakefulness, free of interictal abnormalities, and quantified power in high‐ and low‐alpha bands. Analysis of covariance and post hoc <jats:italic>t</jats:italic>‐tests were used to assess group differences in alpha‐power shift across all <jats:styled-content style="fixed-case">EEG</jats:styled-content> channels. Permutation‐based statistics were used to assess the topography of this shift across the whole scalp.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>Compared to HS, patients showed a statistically significant shift of spectral power from high‐ to low‐alpha frequencies (effect size <jats:italic>g</jats:italic> = 0.78 [95% confidence interval 0.43, 1.20]). This alpha‐power shift was driven by patients with poor seizure control in both <jats:styled-content style="fixed-case">FE</jats:styled-content> and <jats:styled-content style="fixed-case">IGE</jats:styled-content> (<jats:italic>g</jats:italic> = 1.14, [0.65, 1.74]), and occurred over midline frontal and bilateral occipital regions. <jats:styled-content style="fixed-case">IGE</jats:styled-content> exhibited less alpha power shift compared to <jats:styled-content style="fixed-case">FE</jats:styled-content> over bilateral frontal regions (<jats:italic>g</jats:italic> = −1.16 [−0.68, −1.74]). There was no interaction between syndrome and seizure control. Effects were independent of antiepileptic drug load, time of day, or subgroup definitions.</jats:p></jats:sec><jats:sec><jats:title>Interpretation</jats:title><jats:p>Alpha slowing and anteriorization are a robust finding in patients with epilepsy and might represent a generic indicator of seizure liability.</jats:p></jats:sec>

dc.format.extent333-343
dc.format.mediumElectronic-eCollection
dc.languageen
dc.language.isoeng
dc.publisherWiley
dc.subjectAdolescent
dc.subjectAdult
dc.subjectAlpha Rhythm
dc.subjectElectroencephalography
dc.subjectEpilepsy
dc.subjectEpilepsy, Generalized
dc.subjectFemale
dc.subjectFrontal Lobe
dc.subjectHumans
dc.subjectImage Processing, Computer-Assisted
dc.subjectMale
dc.subjectMiddle Aged
dc.subjectSeizures
dc.subjectYoung Adult
dc.titleSlower alpha rhythm associates with poorer seizure control in epilepsy
dc.typejournal-article
dc.typeJournal Article
dc.typeResearch Support, Non-U.S. Gov't
plymouth.author-urlhttps://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000459708100012&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=11bb513d99f797142bcfeffcc58ea008
plymouth.issue2
plymouth.volume6
plymouth.publication-statusPublished
plymouth.journalAnnals of Clinical and Translational Neurology
dc.identifier.doi10.1002/acn3.710
plymouth.organisational-group/Plymouth
plymouth.organisational-group/Plymouth/Faculty of Health
plymouth.organisational-group/Plymouth/Faculty of Health/School of Psychology
plymouth.organisational-group/Plymouth/Users by role
plymouth.organisational-group/Plymouth/Users by role/Academics
dc.publisher.placeUnited States
dcterms.dateAccepted2018-11-26
dc.rights.embargodate2023-2-21
dc.identifier.eissn2328-9503
dc.rights.embargoperiodNot known
rioxxterms.versionofrecord10.1002/acn3.710
rioxxterms.licenseref.urihttp://www.rioxx.net/licenses/all-rights-reserved
rioxxterms.licenseref.startdate2019-02
rioxxterms.typeJournal Article/Review


Files in this item

Thumbnail
Thumbnail

This item appears in the following Collection(s)

Show simple item record


All items in PEARL are protected by copyright law.
Author manuscripts deposited to comply with open access mandates are made available in accordance with publisher policies. Please cite only the published version using the details provided on the item record or document. In the absence of an open licence (e.g. Creative Commons), permissions for further reuse of content should be sought from the publisher or author.
Theme by 
Atmire NV