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ID 65507
フルテキストURL
著者
Akiyama, Mari Department of Child Neurology, Okayama University Hospital
Akiyama, Tomoyuki Department of Paediatrics (Child Neurology), Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences Kaken ID researchmap
Saigusa, Daisuke Tohoku Medical Megabank Organization, Tohoku University
Hishinuma, Eiji Tohoku Medical Megabank Organization, Tohoku University
Matsukawa, Naomi Tohoku Medical Megabank Organization, Tohoku University
Shibata, Takashi Department of Child Neurology, Okayama University Hospital
Tsuchiya, Hiroki Department of Child Neurology, Okayama University Hospital
Mori, Atsushi Department of Neurology, Shiga Medical Centre for Children
Fujii, Yuji Department of Paediatrics, Hiroshima City Funairi Citizens Hospital
Mogami, Yukiko Department of Paediatric Neurology, Osaka Women's and Children's Hospital
Tokorodani, Chiho Department of Paediatrics, Kochi Health Sciences Centre
Kuwahara, Kozue Department of Paediatrics, Ehime Prefectural Central Hospital,
Numata-Uematsu, Yurika Department of Paediatrics, Tohoku University School of Medicine
Inoue, Kenji Department of Neurology, Shiga Medical Centre for Children
Kobayashi, Katsuhiro Department of Paediatrics (Child Neurology), Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences Kaken ID publons researchmap
抄録
Objective: The ketogenic diet (KD), a high-fat and low-carbohydrate diet, is effective for a subset of patients with drug-resistant epilepsy, although the mechanisms of the KD have not been fully elucidated. The aims of this observational study were to investigate comprehensive short-term metabolic changes induced by the KD and to explore candidate metabolites or pathways for potential new therapeutic targets.
Methods: Subjects included patients with intractable epilepsy who had undergone the KD therapy (the medium-chain triglyceride [MCT] KD or the modified Atkins diet using MCT oil). Plasma and urine samples were obtained before and at 2–4 weeks after initiation of the KD. Targeted metabolome analyses of these samples were performed using gas chromatography-tandem mass spectrometry (GC/MS/MS) and liquid chromatography-tandem mass spectrometry (LC/MS/MS).
Results: Samples from 10 and 11 patients were analysed using GC/MS/MS and LC/MS/MS, respectively. The KD increased ketone bodies, various fatty acids, lipids, and their conjugates. In addition, levels of metabolites located upstream of acetyl-CoA and propionyl-CoA, including catabolites of branched-chain amino acids and structural analogues of γ-aminobutyric acid and lactic acid, were elevated.
Conclusions: The metabolites that were significantly changed after the initiation of the KD and related metabolites may be candidates for further studies for neuronal actions to develop new anti-seizure medications.
キーワード
Amino acids
Biomarkers
Intractable epilepsy
Ketone bodies
Organic acids
備考
© 2023 British Epilepsy Association. This manuscript version is made available under the CC-BY-NC-ND 4.0 License. http://creativecommons.org/licenses/by-nc-nd/4.0/. This is the accepted manuscript version. The formal published version is available at https://doi.org/10.1016/j.seizure.2023.03.014.
This fulltext file will be available in Apr. 2024.
発行日
2023-04
出版物タイトル
Seizure
107巻
出版者
Elsevier BV
開始ページ
52
終了ページ
59
ISSN
1059-1311
NCID
AA1091615X
資料タイプ
学術雑誌論文
言語
英語
OAI-PMH Set
岡山大学
著作権者
© 2023 British Epilepsy Association.
論文のバージョン
author
PubMed ID
DOI
Web of Science KeyUT
関連URL
isVersionOf https://doi.org/10.1016/j.seizure.2023.03.014
ライセンス
http://creativecommons.org/licenses/by-nc-nd/4.0/
助成機関名
Japan Epilepsy Research Foundation
Ministry of Education, Culture, Sports, Science and Technology
Japan Agency for Medical Research and Development
Japan Society for the Promotion of Science
助成番号
JERF TENKAN 19001
JP20km0105001
JP21tm0124005
JP20H03374