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Phaseâ amplitude coupling between interictal highâ frequency activity and slow waves in epilepsy surgery

dc.contributor.authorMotoi, Hirotaka
dc.contributor.authorMiyakoshi, Makoto
dc.contributor.authorAbel, Taylor J.
dc.contributor.authorJeong, Jeong‐won
dc.contributor.authorNakai, Yasuo
dc.contributor.authorSugiura, Ayaka
dc.contributor.authorLuat, Aimee F.
dc.contributor.authorAgarwal, Rajkumar
dc.contributor.authorSood, Sandeep
dc.contributor.authorAsano, Eishi
dc.date.accessioned2018-11-20T15:34:58Z
dc.date.available2019-12-02T14:55:09Zen
dc.date.issued2018-10
dc.identifier.citationMotoi, Hirotaka; Miyakoshi, Makoto; Abel, Taylor J.; Jeong, Jeong‐won ; Nakai, Yasuo; Sugiura, Ayaka; Luat, Aimee F.; Agarwal, Rajkumar; Sood, Sandeep; Asano, Eishi (2018). "Phaseâ amplitude coupling between interictal highâ frequency activity and slow waves in epilepsy surgery." Epilepsia 59(10): 1954-1965.
dc.identifier.issn0013-9580
dc.identifier.issn1528-1167
dc.identifier.urihttps://hdl.handle.net/2027.42/146440
dc.description.abstractObjectiveWe hypothesized that the modulation index (MI), a summary measure of the strength of phaseâ amplitude coupling between highâ frequency activity (>150 Hz) and the phase of slow waves (3â 4 Hz), would serve as a useful interictal biomarker for epilepsy presurgical evaluation.MethodsWe investigated 123 patients who underwent focal cortical resection following extraoperative electrocorticography recording and had at least 1 year of postoperative followâ up. We examined whether consideration of MI would improve the prediction of postoperative seizure outcome. MI was measured at each intracranial electrode site during interictal slowâ wave sleep. We compared the accuracy of prediction of patients achieving International League Against Epilepsy class 1 outcome between the full multivariate logistic regression model incorporating MI in addition to conventional clinical, seizure onset zone (SOZ), and neuroimaging variables, and the reduced logistic regression model incorporating all variables other than MI.ResultsNinety patients had class 1 outcome at the time of most recent followâ up (mean followâ up = 5.7 years). The full model had a noteworthy outcome predictive ability, as reflected by regression model fit R2 of 0.409 and area under the curve (AUC) of receiver operating characteristic plot of 0.838. Incomplete resection of SOZ (P < 0.001), larger number of antiepileptic drugs at the time of surgery (P = 0.007), and larger MI in nonresected tissues relative to that in resected tissue (P = 0.020) were independently associated with a reduced probability of class 1 outcome. The reduced model had a lower predictive ability as reflected by R2 of 0.266 and AUC of 0.767. Anatomical variability in MI existed among nonepileptic electrode sites, defined as those unaffected by magnetic resonance imaging lesion, SOZ, or interictal spike discharges. With MI adjusted for anatomical variability, the full model yielded the outcome predictive ability of R2 of 0.422, AUC of 0.844, and sensitivity/specificity of 0.86/0.76.SignificanceMI during interictal recording may provide useful information for the prediction of postoperative seizure outcome.
dc.publisherWiley Periodicals, Inc.
dc.subject.otherepileptogenic zone
dc.subject.otherhighâ frequency oscillations
dc.subject.otherinvasive recording
dc.subject.otherirritative zone
dc.subject.othervideoâ EEG monitoring
dc.titlePhaseâ amplitude coupling between interictal highâ frequency activity and slow waves in epilepsy surgery
dc.typeArticleen_US
dc.rights.robotsIndexNoFollow
dc.subject.hlbsecondlevelMedicine (General)
dc.subject.hlbtoplevelHealth Sciences
dc.description.peerreviewedPeer Reviewed
dc.description.bitstreamurlhttps://deepblue.lib.umich.edu/bitstream/2027.42/146440/1/epi14544_am.pdf
dc.description.bitstreamurlhttps://deepblue.lib.umich.edu/bitstream/2027.42/146440/2/epi14544.pdf
dc.identifier.doi10.1111/epi.14544
dc.identifier.sourceEpilepsia
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dc.owningcollnameInterdisciplinary and Peer-Reviewed


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