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dc.contributor.authorKim, Jeong-Youn-
dc.contributor.authorShin, Jeongyoon-
dc.contributor.authorKim, Laehyun-
dc.contributor.authorKim, Se Hee-
dc.date.accessioned2024-01-12T06:34:24Z-
dc.date.available2024-01-12T06:34:24Z-
dc.date.created2023-09-08-
dc.date.issued2023-09-
dc.identifier.issn1664-2295-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/79843-
dc.description.abstractObjective: To investigate the quantitative electroencephalography (EEG) features associated with a high risk of sudden unexpected death in epilepsy (SUDEP) in patients with Dravet syndrome (DS). Methods: Patients with DS and healthy controls (HCs) who underwent EEG were included in the study. EEG signals were recorded using a 21 channel digital EEG system, and pre-processed data were analyzed to identify quantitative EEG features associated with a high SUDEP risk. To assess the risk of SUDEP, SUDEP-7 scores were used. Results: A total of 64 patients with DS [38 males and 26 females, aged: 128.51?±?75.50?months (range: 23?380?months)], and 13 HCs [7 males and 6 females, aged: 95.46?±?86.48?months (range: 13?263?months)] were included. For the absolute band power, the theta power was significantly higher in the high-SUDEP group than in the low-SUDEP group in the central brain region. For the relative band power, the theta power was also significantly higher in the high-SUDEP group than in the low-SUDEP group in the central and occipital brain regions. The alpha power was significantly lower in the high-SUDEP group than in the low-SUDEP group in the central and parietal brain regions. Conclusion: Patients with high SUDEP-7 scores have different EEG features from those with low SUDEP-7 scores, suggesting that EEG may be used as a biomarker of SUDEP in DS. Significance: Early intervention in patients with DS at a high risk of SUDEP can reduce mortality and morbidity. Patients with high theta band powers warrant high-level supervision.-
dc.languageEnglish-
dc.publisherFrontiers Media S.A.-
dc.titleElectroencephalography characteristics related to risk of sudden unexpected death in epilepsy in patients with Dravet syndrome-
dc.typeArticle-
dc.identifier.doi10.3389/fneur.2023.1222721-
dc.description.journalClass1-
dc.identifier.bibliographicCitationFrontiers in Neurology, v.14-
dc.citation.titleFrontiers in Neurology-
dc.citation.volume14-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid001068389900001-
dc.relation.journalWebOfScienceCategoryClinical Neurology-
dc.relation.journalWebOfScienceCategoryNeurosciences-
dc.relation.journalResearchAreaNeurosciences & Neurology-
dc.type.docTypeArticle-
dc.subject.keywordPlusMOUSE MODEL-
dc.subject.keywordPlusEEG-
dc.subject.keywordPlusMORTALITY-
dc.subject.keywordPlusFEATURES-
dc.subject.keywordPlusRHYTHMS-
dc.subject.keywordPlusSCN1A-
dc.subject.keywordAuthorepilepsy-
dc.subject.keywordAuthorDravet syndrome (DS)-
dc.subject.keywordAuthorsudden unexpected death in epilepsy (SUDEP)-
dc.subject.keywordAuthorelectroencephalography (EEG)-
dc.subject.keywordAuthormortality-
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