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dc.contributor.authorÇokyaman, Turgay
dc.contributor.authorKasap, Tolga
dc.contributor.authorŞehitoğlu, Hilal
dc.date.accessioned2023-04-18T08:45:35Z
dc.date.available2023-04-18T08:45:35Z
dc.date.issued2021en_US
dc.identifier.citationCokyaman, T., Kasap, T., & Şehitoğlu, H. (2021). Serum brain‐derived neurotrophic factor in the diagnosis of febrile seizure. Pediatrics International, 63(9), 1082–1086. https://doi.org/10.1111/ped.14567en_US
dc.identifier.issn1328-8067 / 1442-200X
dc.identifier.uridoi:10.1111/ped.14567
dc.identifier.urihttps://hdl.handle.net/20.500.12428/4039
dc.description.abstractBackground Brain-derived neurotrophic factor (BDNF) is a noncovalently linked homodimer protein from the neurotrophic growth factor family. Although it is expressed throughout the brain, it is produced more intensively in the entorhinal cortex and hippocampus and can cross the blood-brain barrier in two directions easily. The aim of this study is to understand, for the first time, whether there is a relationship between febrile seizure (FS) and BDNF. Methods The study included cases diagnosed with FS and febrile illness, of similar age, weight, and height, between 6 months and 6 years. Samples for serum BDNF measurement were taken within the first 24-48 h of admission at the hospital and levels were measured using the commercial enzyme-linked immunosorbent assay kit and expressed in ng/mL. Results Eighty cases (40 FS, 40 febrile illness) were included in the study. The mean serum BDNF was found to be 6.7 +/- 2.4 ng/mL in the FS group and 4.5 +/- 2.6 ng/mL in the febrile illness group (P = 0.001). No relation was found between gender, age, body weight, length, and platelet counts and serum BDNF levels. The optimal cut-off value for serum BDNF was found to be 5.2 ng/mL (75% sensitivity, 62.5% specificity, AUC: 0.723) to distinguish between FS and febrile illness. Conclusions Excluding demographic variables such as gender, age, weight, length, and platelet counts serum BDNF levels have increased in children with FS. Considering the hippocampal origin of FS, we can suggest that the pathophysiology of FS may be related to the BDNF.en_US
dc.language.isoengen_US
dc.publisherJohn Wiley and Sons Incen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBrain-Derived Neurotrophic Factoren_US
dc.subjectChildrenen_US
dc.subjectFebrile Seizureen_US
dc.titleSerum brain-derived neurotrophic factor in the diagnosis of febrile seizureen_US
dc.typearticleen_US
dc.authorid0000-0002-7108-6839en_US
dc.authorid-en_US
dc.authorid0000-0003-4436-9160en_US
dc.relation.ispartofPediatrics Internationalen_US
dc.departmentFakülteler, Güzel Sanatlar Fakültesi, Seramik ve Cam Bölümüen_US
dc.departmentFakülteler, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümüen_US
dc.departmentFakülteler, Tıp Fakültesi, Temel Tıp Bilimleri Bölümüen_US
dc.identifier.volume63en_US
dc.identifier.issue9en_US
dc.identifier.startpage1082en_US
dc.identifier.endpage1086en_US
dc.institutionauthorÇokyaman, Turgay
dc.institutionauthorKasap, Tolga
dc.institutionauthorŞehitoğlu, Hilal
dc.identifier.doi10.1111/ped.14567en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.authorwosidAAP-6709-2021en_US
dc.authorwosidDWC-4842-2022en_US
dc.authorwosidFWG-5628-2022en_US
dc.authorscopusid56422292600en_US
dc.authorscopusid57221477967en_US
dc.authorscopusid57221785513en_US
dc.identifier.wosqualityQ4en_US
dc.identifier.wosWOS:000661029000001en_US
dc.identifier.scopus2-s2.0-85107767128en_US
dc.identifier.pmid33289227en_US


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