Literature DB >> 25096692

Genetic variants associated with phenytoin-related severe cutaneous adverse reactions.

Wen-Hung Chung1, Wan-Chun Chang2, Yun-Shien Lee3, Ying-Ying Wu2, Chih-Hsun Yang4, Hsin-Chun Ho5, Ming-Jing Chen4, Jing-Yi Lin5, Rosaline Chung-Yee Hui4, Ji-Chen Ho6, Wei-Ming Wu6, Ting-Jui Chen7, Tony Wu8, Yih-Ru Wu8, Mo-Song Hsih8, Po-Hsun Tu9, Chen-Nen Chang9, Chien-Ning Hsu10, Tsu-Lan Wu11, Siew-Eng Choon12, Chao-Kai Hsu13, Der-Yuan Chen14, Chin-San Liu15, Ching-Yuang Lin16, Nahoko Kaniwa17, Yoshiro Saito17, Yukitoshi Takahashi18, Ryosuke Nakamura17, Hiroaki Azukizawa19, Yongyong Shi20, Tzu-Hao Wang21, Shiow-Shuh Chuang22, Shih-Feng Tsai23, Chee-Jen Chang24, Yu-Sun Chang25, Shuen-Iu Hung2.   

Abstract

IMPORTANCE: The antiepileptic drug phenytoin can cause cutaneous adverse reactions, ranging from maculopapular exanthema to severe cutaneous adverse reactions, which include drug reactions with eosinophilia and systemic symptoms, Stevens-Johnson syndrome, and toxic epidermal necrolysis. The pharmacogenomic basis of phenytoin-related severe cutaneous adverse reactions remains unknown.
OBJECTIVE: To investigate the genetic factors associated with phenytoin-related severe cutaneous adverse reactions. DESIGN, SETTING, AND PARTICIPANTS: Case-control study conducted in 2002-2014 among 105 cases with phenytoin-related severe cutaneous adverse reactions (n=61 Stevens-Johnson syndrome/toxic epidermal necrolysis and n=44 drug reactions with eosinophilia and systemic symptoms), 78 cases with maculopapular exanthema, 130 phenytoin-tolerant control participants, and 3655 population controls from Taiwan, Japan, and Malaysia. A genome-wide association study (GWAS), direct sequencing of the associated loci, and replication analysis were conducted using the samples from Taiwan. The initial GWAS included samples of 60 cases with phenytoin-related severe cutaneous adverse reactions and 412 population controls from Taiwan. The results were validated in (1) 30 cases with severe cutaneous adverse reactions and 130 phenytoin-tolerant controls from Taiwan, (2) 9 patients with Stevens-Johnson syndrome/toxic epidermal necrolysis and 2869 population controls from Japan, and (3) 6 cases and 374 population controls from Malaysia. MAIN OUTCOMES AND MEASURES: Specific genetic factors associated with phenytoin-related severe cutaneous adverse reactions.
RESULTS: The GWAS discovered a cluster of 16 single-nucleotide polymorphisms in CYP2C genes at 10q23.33 that reached genome-wide significance. Direct sequencing of CYP2C identified missense variant rs1057910 (CYP2C9*3) that showed significant association with phenytoin-related severe cutaneous adverse reactions (odds ratio, 12; 95% CI, 6.6-20; P=1.1 × 10(-17)). The statistically significant association between CYP2C9*3 and phenytoin-related severe cutaneous adverse reactions was observed in additional samples from Taiwan, Japan, and Malaysia. A meta-analysis using the data from the 3 populations showed an overall odds ratio of 11 (95% CI, 6.2-18; z=8.58; P < .00001) for CYP2C9*3 association with phenytoin-related severe cutaneous adverse reactions. Delayed clearance of plasma phenytoin was detected in patients with severe cutaneous adverse reactions, especially CYP2C9*3 carriers, providing a functional link of the associated variants to the disease. CONCLUSIONS AND RELEVANCE: This study identified CYP2C variants, including CYP2C9*3, known to reduce drug clearance, as important genetic factors associated with phenytoin-related severe cutaneous adverse reactions.

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Year:  2014        PMID: 25096692     DOI: 10.1001/jama.2014.7859

Source DB:  PubMed          Journal:  JAMA        ISSN: 0098-7484            Impact factor:   56.272


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