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dc.contributor.authorTüray, Sevim
dc.contributor.authorCangür, Şengül
dc.contributor.authorKahraman, Gözde
dc.contributor.authorKayabaşı, Eda
dc.contributor.authorÇetiner, Ömer Faruk
dc.contributor.authorAydın, Burak
dc.contributor.authorÖztürk, Cihadiye Elif
dc.date.accessioned2023-06-05T07:29:54Z
dc.date.available2023-06-05T07:29:54Z
dc.date.issued2023en_US
dc.identifier.citationTuray, S., Cangur, S., Kahraman, G., Kayabasi, E., Cetiner, O. F., Aydin, B., & Ozturk, C. E. (2023). Can the gut microbiota serve as a guide to the diagnosis and treatment of childhood epilepsy?. Pediatric Neurology.en_US
dc.identifier.issn0887-8994
dc.identifier.urihttps://doi.org/10.1016/j.pediatrneurol.2023.04.006
dc.identifier.urihttps://hdl.handle.net/20.500.12294/3883
dc.description.abstractBackground: To investigate the activity of the gut-brain axis in the pathogenesis of childhood epilepsy and to define biomarkers capable of assisting with determining new strategies in that context. Methods: Twenty children with epilepsy of “unknown etiology” and seven healthy controls in the same age group were included in the study. The groups were compared using a questionnaire. Stool samples were stored in tubes containing DNA/RNA Shield (Zymo Research) with a sterile swab. Sequencing was carried out using the MiSeq System (Illumina). The 16S rRNA sequencing of samples using next-generation sequencing involved V4 variable region polymerase chain reaction amplification concluded by 2 × 250-bp paired-end sequencing of amplicons and at least 50,000 reads (>Q30) per sample. DNA sequences were classified at the genus level using the Kraken program. Bioinformatics and statistical analysis were then performed. Results: Individuals’ gut microbiota relative abundance values differed between the groups at the genus, order, class, family, and phylum levels. Flavihumibacter, Niabella, Anoxybacillus, Brevundimonas, Devosia, and Delftia were seen only in the control group, whereas Megamonas and Coriobacterium were observed only in the epilepsy group. The linear discriminant analysis effect size method identified 33 taxa as important in differentiating the groups. Conclusions: We think that bacterial varieties (such as Megamonas and Coriobacterium) that differ between the two groups can be employed as useful biomarkers in the diagnosis and follow-up of epileptic patients. We also predict that, in addition to epilepsy treatment protocols, the restoration of eubiotic microbiota may increase the success of treatment. © 2023 Elsevier Inc.en_US
dc.language.isoengen_US
dc.publisherElsevier Inc.en_US
dc.relation.ispartofPediatric Neurologyen_US
dc.identifier.doi10.1016/j.pediatrneurol.2023.04.006en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBiomarkeren_US
dc.subjectChildhood Epilepsyen_US
dc.subjectDiagnosisen_US
dc.subjectGut Microbiotaen_US
dc.subjectSeizure Controlen_US
dc.subjectTreatmenten_US
dc.titleCan the Gut Microbiota Serve as a Guide to the Diagnosis and Treatment of Childhood Epilepsy?en_US
dc.typearticleen_US
dc.departmentTıp Fakültesi, Temel Tıp Bilimleri Bölümüen_US
dc.identifier.volume145en_US
dc.identifier.startpage11en_US
dc.identifier.endpage21en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.institutionauthorÖztürk, Cihadiye Elif
dc.authorscopusid35571535100en_US
dc.identifier.scopus2-s2.0-85160321548en_US


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