4.6 Review

Clinical Pharmacogenetics Implementation Consortium (CPIC) Guideline forCYP2C9andHLA-BGenotypes and Phenytoin Dosing: 2020 Update

期刊

CLINICAL PHARMACOLOGY & THERAPEUTICS
卷 109, 期 2, 页码 302-309

出版社

WILEY
DOI: 10.1002/cpt.2008

关键词

-

资金

  1. National Institutes of Health (NIH) [R24GM115264, U24HG010135, R24 GM61374, R24GM123930, GM092666, GM32165, UO1 GM092676, U01 HL0105918]
  2. NIH's National Heart Lung and Blood Institute (NHLBI) [K01HL143137]
  3. American College of Clinical Pharmacy
  4. Flinn Foundation
  5. National Health and Medical Research Council of Australia [APP108798]
  6. NIH [R01 HG010863-01, 1P50GM115305-01, R21AI139021, R34AI136815]
  7. NHMRC [APP1123499]

向作者/读者索取更多资源

Phenytoin, an antiepileptic drug, is influenced by genetic variations in patients, with individuals carrying the variant allele HLA-B*15:02 having an increased risk of severe skin reactions when receiving phenytoin treatment.
Phenytoin is an antiepileptic drug with a narrow therapeutic index and large interpatient pharmacokinetic variability, partly due to genetic variation inCYP2C9. Furthermore, the variant alleleHLA-B*15:02is associated with an increased risk of Stevens-Johnson syndrome and toxic epidermal necrolysis in response to phenytoin treatment. We summarize evidence from the published literature supporting these associations and provide therapeutic recommendations for the use of phenytoin based onCYP2C9and/orHLA-Bgenotypes (updates on cpicpgx.org).

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据