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

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...

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Veröffentlicht in:Pharmacogenetics and genomics 2011-05, Vol.21 (5), p.303-307
Hauptverfasser: Kang, Hye-Ryun, 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
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Sprache:eng
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Zusammenfassung: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%, Pc=2.45×10, odds ratio (OR)=97.8], Cw*0302 (92.0 vs. 12.3%, Pc=9.39×10, OR=82.1), and A*3303 (88.0 vs. 26.3%, Pc=3.31×10, 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.
ISSN:1744-6872
1744-6880
DOI:10.1097/FPC.0b013e32834282b8