Allergy Asthma Immunol Res. 2012;4(3):132-6.
Genetic Variations in TXNRD1 as Potential Predictors of Drug-Induced Liver Injury.
제1저자 권재우 · 교신저자 박흥우
소속 (1)
- Department of Internal Medicine, Seoul National University College of Medicine, Seoul, Korea.
Abstract
PURPOSE Drug-induced liver injury (DILI) is the most common adverse drug reaction; however, it is not easily predicted. We hypothesize that DILI has a common genetic basis. Based on the findings of previous animal studies on toxic hepatitis, we selected the thioredoxin reductase 1 gene (TXNRD1) as a candidate marker of DILI for this genetic association study.
METHODS Records from 118 patients with DILI were extracted from the database of the Adverse Drug Reaction Research Group in South Korea. Causative drugs included antituberculosis drugs (n=68, 57.6%), antibiotics (n=22, 18.6%), antiepileptic drugs (n=7, 5.9%), non-steroidal anti-inflammatory drugs (n=5, 4.2%), and others (n=16, 13.7%). Seven single nucleotide polymorphisms (SNPs) in TXNRD1 (rs10735393, rs4964287, rs4595619, rs10861201, rs11111997, rs4246270, and rs4246271) were scored in 118 DILI patients and in 120 drug-matched controls without liver injury.
RESULTS No differences were found between the frequencies of any of the 7 SNPs in the cases and controls; however, a significant association was found between a TTA haplotype composed of rs10735393, rs4964287, and rs4595619 and DILI using an allele model (odds ratio, 1.79; 95% confidence interval, 1.18-2.73; P=0.008; Bonferroni corrected P=0.024).
CONCLUSIONS These results suggest that genetic variations in TXNRD1 favor the development of DILI, although a larger confirmative study is needed.
Keywords
Drug-induced liver injurygenetic association studygenetic polymorphismsingle nucleotide polymorphismsthioredoxin reductase 1
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그림 출처: PubMed Central 공개 논문 (PMC3328729)
Conflict of interest statement
There are no financial or other issues that might lead to conflict of interest.
그 밖의 정보
- 출판 형태
- Journal Article
- 저널
- Allergy, asthma & immunology research · eISSN 2092-7363
- 전자 출판
- 2011-11-10
- 참고문헌
- 20편