Niwat SaksitWichittra TassaneeyakulNontaya NakkamParinya KonyoungUsanee KhunarkornsiriPansu ChumworathayiChonlaphat SukasemSumitra SuttisaiNapacha PiriyachananusornPawinee TiwongNathorn ChaiyakunaprukKittisak SawanyawisuthTicha RerkpattanapipatWongwiwat TassaneeyakulKhon Kaen UniversityPharmacy UnitFaculty of MedicineResearch and Diagnostic Center for Emerging Infectious DiseasesResearch Center in BackSleep Apnea Research GroupUniversity of PhayaoUdon Thani Center HospitalDivision of Pharmacogenomics and Personalized MedicineSomdech Phra Debaratana Medical CenterMahidol UniversityPhrae HospitalNaresuan UniversitySchool of PharmacyMonash University MalaysiaUniversity of Wisconsin Madison2018-12-212019-03-142018-12-212019-03-142017-01-01Pharmacogenetics and Genomics. Vol.27, No.7 (2017), 255-26317446880174468722-s2.0-85019608236https://repository.li.mahidol.ac.th/handle/20.500.14594/42106Copyright © 2017 Wolters Kluwer Health, Inc. All rights reserved. Background Allopurinol is one of the most common causes of severe cutaneous adverse drug reactions (SCARs) including drug reactions with eosinophilia and systemic symptoms (DRESS), Stevens-Johnson syndrome (SJS), and toxic epidermal necrolysis (TEN). This study identified the risk factors associated with the development of allopurinol-induced SCARs in a Thai population. Patients and methods Eighty-six allopurinol-induced SCARs (i.e. 19 DRESS and 67 SJS/TEN) and 182 allopurinol-tolerant patients were enrolled in the study. The HLA-B∗58:01 allele was determined. Clinical and medicinal data were collected. Results Results from multivariate analysis showed that only the HLA-B∗58:01 and female sex were identified as risk factors of allopurinol-induced SCARs in this Thai population. Patients who carried the HLA-B∗58:01 allele were at a higher risk of allopurinol-induced DRESS [odds ratio (OR)=149.2, 95% confidence interval (CI)=24.0-∞, P<1.00X10-4]. Similar results were observed in allopurinol-induced SJS/TEN (OR=175.0, 95% CI=44.3-690.9, P=1.69X10-13). The risk of allopurinolinduced SCARs in women was higher than that in men (OR=4.6, 95% CI=1.4-15.6, P=1.44×10-2). The overall mortality rate of allopurinol-induced SCARs was 11.39% and a higher mortality rate was observed in elderly women. Conclusion Among the risk factors identified, the HLAB∗58:01 allele had the greatest impact on the development of both phenotypes of allopurinol-induced SCARs in this studied Thai population. In case HLA-B∗58:01 genotyping cannot be accessed, close monitoring of allopurinol usage, especially in elderly women with impaired renal function, is necessary to reduce the mortality rate of these lifethreatening SCARs.Mahidol UniversityBiochemistry, Genetics and Molecular BiologyArticleSCOPUS10.1097/FPC.0000000000000285