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