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Update on the Genetic Polymorphisms of Drug-Metabolizing Enzymes in Antiepileptic Drug Therapy
http://hdl.handle.net/2298/20238
http://hdl.handle.net/2298/20238387fa17f-5585-4047-bce9-80f6846233cd
名前 / ファイル | ライセンス | アクション |
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pharmaceuticals-03-02709.pdf (222.6 kB)
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Item type | 学術雑誌論文 / Journal Article(1) | |||||
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公開日 | 2011-07-12 | |||||
タイトル | ||||||
タイトル | Update on the Genetic Polymorphisms of Drug-Metabolizing Enzymes in Antiepileptic Drug Therapy | |||||
言語 | ||||||
言語 | eng | |||||
キーワード | ||||||
主題 | pharmacogenetics, genetic polymorphisms, antiepileptic drugs, drug-metabolizing enzyme, population pharmacokinetics | |||||
資源タイプ | ||||||
資源タイプ | journal article | |||||
著者 |
Saruwatari, Junji
× Saruwatari, Junji× Ishitsu, Takateru× Nakagawa, Kazuko |
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別言語の著者 |
猿渡, 淳二
× 猿渡, 淳二× 石津, 棟暎× 中川, 和子 |
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内容記述 | ||||||
内容記述 | Genetic polymorphisms in the genes that encode drug-metabolizing enzymes are implicated in the inter-individual variability in the pharmacokinetics and pharmaco-dynamics of antiepileptic drugs (AEDs). However, the clinical impact of these polymorphisms on AED therapy still remains controversial. The defective alleles of cytochrome P450 (CYP) 2C9 and/or CYP2C19 could affect not only the pharmacokinetics, but also the pharmacodynamics of phenytoin therapy. CYP2C19 deficient genotypes were associated with the higher serum concentration of an active metabolite of clobazam, N-desmethylclobazam, and with the higher clinical efficacy of clobazam therapy than the other CYP2C19 genotypes. The defective alleles of CYP2C9 and/or CYP2C19 were also found to have clinically significant effects on the inter-individual variabilities in the population pharmacokinetics of phenobarbital, valproic acid and zonisamide. EPHX1 polymorphisms may be associated with the pharmacokinetics of carbamazepine and the risk of phenytoin-induced congenital malformations. Similarly, the UDP-glucuronosyltransferase 2B7 genotype may affect the pharmacokinetics of lamotrigine. Gluthatione S-transferase null genotypes are implicated in an increased risk of hepatotoxicity caused by carbamazepine and valproic acid. This article summarizes the state of research on the effects of mutations of drug-metabolizing enzymes on the pharmacokinetics and pharmacodynamics of AED therapies. Future directions for the dose-adjustment of AED are discussed. | |||||
書誌情報 |
Pharmaceuticals 巻 3, 号 8, p. 2709-2732, 発行年 2010-08-20 |
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DOI | ||||||
関連タイプ | isIdenticalTo | |||||
関連識別子 | 10.3390/ph3082709 | |||||
情報源(ISSN) | ||||||
関連名称 | 14248247 | |||||
フォーマット | ||||||
内容記述 | application/pdf | |||||
形態 | ||||||
222588 bytes | ||||||
著者版フラグ | ||||||
出版タイプ | VoR | |||||
日本十進分類法 | ||||||
主題 | 499 | |||||
出版者 | ||||||
出版者 | MDPI Publishing | |||||
資源タイプ | ||||||
内容記述 | 論文(Article) | |||||
資源タイプ・ローカル | ||||||
雑誌掲載論文 | ||||||
資源タイプ・NII | ||||||
Journal Article | ||||||
資源タイプ・DCMI | ||||||
text | ||||||
資源タイプ・ローカル表示コード | ||||||
01 | ||||||
URL | ||||||
内容記述 | http://www.mdpi.com/1424-8247/3/8/2709/ |