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Vitamin B6 in acute encephalopathy with biphasic seizures and late reduced diffusion.
Akiyama, Tomoyuki; Toda, Soichiro; Kimura, Nobusuke; Mogami, Yukiko; Hanaoka, Yoshiyuki; Tokorodani, Chiho; Ito, Tomoshiro; Miyahara, Hiroyuki; Hyodo, Yuki; Kobayashi, Katsuhiro.
Afiliación
  • Akiyama T; Department of Child Neurology, Okayama University Hospital, Okayama, Japan; Department of Child Neurology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan. Electronic address: takiyama@okayama-u.ac.jp.
  • Toda S; Department of Pediatrics, Kameda Medical Center, Chiba, Japan.
  • Kimura N; Department of Pediatrics, Japanese Red Cross Otsu Hospital, Shiga, Japan.
  • Mogami Y; Department of Pediatric Neurology, Osaka Women's and Children's Hospital, Osaka, Japan.
  • Hanaoka Y; Department of Child Neurology, Okayama University Hospital, Okayama, Japan.
  • Tokorodani C; Department of Pediatrics, Kochi Health Sciences Center, Kochi, Japan.
  • Ito T; Department of Pediatrics, Sapporo City General Hospital, Hokkaido, Japan.
  • Miyahara H; Department of Pediatrics, Kurashiki Central Hospital, Okayama, Japan.
  • Hyodo Y; Department of Child Neurology, Okayama University Hospital, Okayama, Japan; Department of Child Neurology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.
  • Kobayashi K; Department of Child Neurology, Okayama University Hospital, Okayama, Japan; Department of Child Neurology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.
Brain Dev ; 42(5): 402-407, 2020 May.
Article en En | MEDLINE | ID: mdl-32107100
BACKGROUND: The initial presentation of acute encephalopathy with biphasic seizures and late reduced diffusion (AESD) is indistinguishable from that of complex febrile seizures (FS), which poses a great diagnostic challenge for clinicians. Excitotoxicity is speculated to be the pathogenesis of AESD. Vitamin B6 (VB6) is essential for the biosynthesis of gamma-aminobutyric acid, an inhibitory neurotransmitter. The aim of this study is to investigate our hypothesis that VB6 deficiency in the brain may play a role in AESD. METHODS: We obtained cerebrospinal fluid (CSF) samples from pediatric patients with AESD after early seizures and those with FS. We measured pyridoxal 5'-phosphate (PLP) and pyridoxal (PL) concentrations in the CSF samples using high-performance liquid chromatography with fluorescence detection. RESULTS: The subjects were 5 patients with AESD and 17 patients with FS. Age did not differ significantly between AESD and FS. In AESD, CSF PLP concentration was marginally lower (p = 0.0999) and the PLP-to-PL ratio was significantly (p = 0.0417) reduced compared to those in FS. CONCLUSIONS: Although it is impossible to conclude that low PLP concentration and PLP-to-PL ratio are causative of AESD, this may be a risk factor for developing AESD. When combined with other markers, this finding may be useful in distinguishing AESD from FS upon initial presentation.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Piridoxal / Fosfato de Piridoxal / Convulsiones / Encefalopatías Tipo de estudio: Risk_factors_studies Límite: Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Brain Dev Año: 2020 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Piridoxal / Fosfato de Piridoxal / Convulsiones / Encefalopatías Tipo de estudio: Risk_factors_studies Límite: Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Brain Dev Año: 2020 Tipo del documento: Article