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Positive and negative associations of HLA class I alleles with allopurinol-induced SCARs in Koreans.

Authors
  • Kang, Hye-Ryun1
  • Jee, Young Koo
  • Kim, Yon-Soo
  • Lee, Chang Hwa
  • Jung, Jae-Woo
  • Kim, Sae Hoon
  • Park, Heung-Woo
  • Chang, Yoon-Seok
  • Jang, In-Jin
  • Cho, Sang-Heon
  • Min, Kyung-Up
  • Kim, Sang-Heon
  • Lee, Kyung Wha
  • 1 Department of Internal Medicine, Seoul National University College of Medicine, Seoul, Korea. , (North Korea)
Type
Published Article
Journal
Pharmacogenetics and genomics
Publication Date
May 01, 2011
Volume
21
Issue
5
Pages
303–307
Identifiers
DOI: 10.1097/FPC.0b013e32834282b8
PMID: 21301380
Source
Medline
License
Unknown

Abstract

Recent investigations suggest genetic susceptibility of allopurinol-induced severe cutaneous adverse reactions (SCARs). However, the strength of association was variable according to phenotypes and ethnic backgrounds. To explore genetic markers for allopurinol-induced SCARs in Koreans, we genotyped human leukocyte antigen (HLA) class I alleles of 25 cases of allopurinol-induced SCARs (20 cases of drug-induced hypersensitivity syndrome and five cases of Stevens-Johnson syndrome/toxic epidermal necrolysis) and 57 patients tolerant to allopurinol. Frequencies of B*5801 [92.0 vs. 10.5%, P(c)=2.45×10(-11), odds ratio (OR)=97.8], Cw*0302 (92.0 vs. 12.3%, P(c)=9.39×10(-11), OR=82.1), and A*3303 (88.0 vs. 26.3%, P(c)=3.31×10(-6), OR=20.5) were significantly higher in SCARs compared with tolerant controls. In contrast, A*0201 was not found in SCARs patients despite relatively high frequency in tolerant controls (29.8%). We found strong positive association of HLA-B*5801 and negative association of HLA-A*0201 with the development of allopurinol-induced SCARs in the Korean population.

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