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ID 71219
フルテキストURL
著者
Kitagawa, Kohei Department of Neuropsychiatry, Okayama Psychiatric Medical Center
Nawa, Hideki Department of Pharmacy, Faculty of Pharmacy, Shujitsu University
Asai, Shota Department of Pharmacy, Faculty of Pharmacy, Shujitsu University
Iwata, Naohiro Department of Pharmacy, Okayama University Hospital
Niimura, Takahiro Department of Clinical Pharmacology and Therapeutics, Tokushima University Graduate School of Biomedical Sciences
Hamano, Hirofumi Department of Pharmacy, Okayama University Hospital
Goda, Mitsuhiro Department of Clinical Pharmacology and Therapeutics, Graduate School of Biomedical and Health Sciences, Hiroshima University
Zamami, Yoshito Department of Pharmacy, Okayama University Hospital ORCID Kaken ID publons researchmap
Ishizawa, Keisuke Department of Clinical Pharmacology and Therapeutics, Tokushima University Graduate School of Biomedical Sciences
抄録
Huntington’s disease (HD) is a progressive neurodegenerative disorder characterized by motor, cognitive, and psychiatric symptoms. Tetrabenazine (TBZ), a vesicular monoamine transporter 2 inhibitor, is commonly used to manage chorea; however, it may exhibit fluctuating plasma levels and elicit frequent adverse events. In this study, we aimed to clarify the effects of TBZ deuteration on its safety profile. We compared the safety profiles of TBZ and deutetrabenazine (DTBZ) in real-world clinical practice using disproportionality analysis and the large-scale pharmacovigilance database, VigiBase—the WHO’s global database of adverse drug reactions. Adverse event signals were assessed using the information component (IC). Seriousness was classified according to clinical outcome, and time to onset (TTO) was analyzed for selected events. TBZ showed signals for disorientation, dystonia, and sleep disorders (IC025 > 0), whereas DTBZ did not. Serious adverse events were reported in 54.7% of TBZ cases and 37.9% of DTBZ cases. The TTO of sleep disorder was also evaluated; however, the number of cases with available TTO information was limited. DTBZ showed fewer adverse event signals and a lower proportion of serious adverse events than TBZ. These findings suggest potential differences in the safety profiles of the two drugs, which may influence tolerability in the treatment of HD.
キーワード
deuterated drug
VigiBase
heavy drug
safety advantage
pharmacovigilance analysis
発行日
2026-06-20
出版物タイトル
Biological and Pharmaceutical Bulletin
巻
49巻
号
6号
出版者
Pharmaceutical Society of Japan
開始ページ
983
終了ページ
988
ISSN
0918-6158
NCID
AA10885497
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
© 2026 The Author(s).
論文のバージョン
publisher
PubMed ID
DOI
CRID
関連URL
isVersionOf https://doi.org/10.1248/bpb.b25-00768
ライセンス
https://creativecommons.org/licenses/by-nc/4.0/
助成情報
24K09927: 大規模医療情報とオミクスデータを活用した新たな薬剤性間質性肺疾患予防薬の開発 ( 独立行政法人日本学術振興会 / Japan Society for the Promotion of Science )