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dc.contributor.authorYaakub, SN
dc.contributor.authorTangwiriyasakul, C
dc.contributor.authorAbela, E
dc.contributor.authorKoutroumanidis, M
dc.contributor.authorElwes, RDC
dc.contributor.authorBarker, GJ
dc.contributor.authorRichardson, MP
dc.date.accessioned2023-02-20T14:51:36Z
dc.date.issued2020-04-25
dc.identifier.issn2328-9503
dc.identifier.issn2328-9503
dc.identifier.urihttp://hdl.handle.net/10026.1/20479
dc.description.abstract

<jats:title>Abstract</jats:title><jats:sec><jats:title>Objective</jats:title><jats:p>Electroencephalography (EEG) features in the alpha band have been shown to differ between people with epilepsy and healthy controls. Here, in a group of patients with mesial temporal lobe epilepsy (mTLE), we seek to confirm these EEG features, and using simultaneous functional magnetic resonance imaging, we investigate whether brain networks related to the alpha rhythm differ between patients and healthy controls. Additionally, we investigate whether alpha abnormalities are found as an inherited endophenotype in asymptomatic relatives.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>We acquired scalp EEG and simultaneous EEG and functional magnetic resonance imaging in 24 unrelated patients with unilateral mTLE, 23 asymptomatic first‐degree relatives of patients with mTLE, and 32 healthy controls. We compared peak alpha power and frequency from electroencephalographic data in patients and relatives to healthy controls. We identified brain networks associated with alpha oscillations and compared these networks in patients and relatives to healthy controls.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>Patients had significantly reduced peak alpha frequency (PAF) across all parietal and occipital electrodes. Asymptomatic relatives also had significantly reduced PAF over 14 of 17 parietal and occipital electrodes. Both patients and asymptomatic relatives showed a combination of increased activation and a failure of deactivation in relation to alpha oscillations compared to healthy controls in the sensorimotor network.</jats:p></jats:sec><jats:sec><jats:title>Interpretation</jats:title><jats:p>Genetic factors may contribute to the shift in PAF and alterations in brain networks related to alpha oscillations. These may not entirely be a consequence of anti‐epileptic drugs, seizures or hippocampal sclerosis and deserve further investigation as mechanistic contributors to mTLE.</jats:p></jats:sec>

dc.format.extent667-676
dc.format.mediumPrint-Electronic
dc.languageen
dc.language.isoeng
dc.publisherWiley
dc.subjectAdult
dc.subjectAlpha Rhythm
dc.subjectElectroencephalography
dc.subjectEpilepsy, Temporal Lobe
dc.subjectFemale
dc.subjectFunctional Neuroimaging
dc.subjectHumans
dc.subjectMagnetic Resonance Imaging
dc.subjectMale
dc.subjectMiddle Aged
dc.subjectNerve Net
dc.subjectOccipital Lobe
dc.subjectParietal Lobe
dc.subjectSensorimotor Cortex
dc.titleHeritability of alpha and sensorimotor network changes in temporal lobe epilepsy
dc.typejournal-article
dc.typeArticle
plymouth.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/32333640
plymouth.issue5
plymouth.volume7
plymouth.publisher-urlhttp://dx.doi.org/10.1002/acn3.51032
plymouth.publication-statusPublished
plymouth.journalAnnals of Clinical and Translational Neurology
dc.identifier.doi10.1002/acn3.51032
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.dateAccepted2020-03-11
dc.rights.embargodate2023-2-21
dc.identifier.eissn2328-9503
dc.rights.embargoperiodNot known
rioxxterms.versionofrecord10.1002/acn3.51032
rioxxterms.licenseref.urihttp://www.rioxx.net/licenses/all-rights-reserved
rioxxterms.licenseref.startdate2020-05
rioxxterms.typeJournal Article/Review


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