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HLA-B*51:01 and CYP2C9*3 Are Risk Factors for Phenytoin-Induced Eruption in the Japanese Population: Analysis of Data From the Biobank Japan Project

  • Keiko Hikino
  • , Takeshi Ozeki
  • , Masaru Koido
  • , Chikashi Terao
  • , Yoichiro Kamatani
  • , Yoshiko Mizukawa
  • , Tetsuo Shiohara
  • , Mikiko Tohyama
  • , Hiroaki Azukizawa
  • , Michiko Aihara
  • , Hiroyuki Nihara
  • , Eishin Morita
  • , Yoshinori Murakami
  • , Michiaki Kubo
  • , Taisei Mushiroda

研究成果: ジャーナルへの寄稿学術論文査読

18   !!Link opens in a new tab 被引用数 (Scopus)

抄録

CYP2C9*3 and HLA-B alleles are reportedly associated with phenytoin-induced eruption in some East Asian populations; however, this finding is not readily applicable to the Japanese population. Thus, we aimed to investigate the risk alleles using samples and data from BioBank Japan. A total of 747 patients (24 cases and 723 tolerant controls) were selected for analysis. Case-control association studies were conducted, using CYP2C9*3, CYP2C9*27, CYP2C19*2, CYP2C19*3, and HLA-B allele genotype data. CYP2C9*3 carrier status was significantly associated with phenytoin-induced eruption (P = 0.0022, odds ratio 7.05, 95% confidence interval, 2.44–20.4). HLA-B*51:01 showed the most prominent association (P = 0.010, odds ratio 3.19, 95% confidence interval, 1.37–7.48). Including both of these features improved predictive performance, measured as area under the receiver operating characteristic curve, by 10%. CYP2C9*3 and HLA-B*51:01 allele carrier statuses are significantly associated with phenytoin-induced eruption; thus, checking this carrier status before prescription would decrease the incidence of phenytoin-induced eruption in clinical practice.

本文言語英語
ページ(範囲)1170-1178
ページ数9
ジャーナルClinical Pharmacology and Therapeutics
107
5
DOI
出版ステータス出版済み - 01-05-2020
外部発表はい

All Science Journal Classification (ASJC) codes

  • 薬理学
  • 薬理学(医学)

フィンガープリント

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