Associations between HLA class i and cytochrome P450 2C9 genetic polymorphisms and phenytoin-related severe cutaneous adverse reactions in a Thai population
© 2016 Wolters Kluwer Health, Inc. All rights reserved. Background Phenytoin is one of the most common causative drugs of several types of severe cutaneous adverse reactions (SCAR) such as Stevens-Johnson syndrome (SJS), toxic epidermal necrolysis (TEN), and drug reactions with eosinophilia and syst...
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th-mahidol.432292019-03-14T15:04:18Z Associations between HLA class i and cytochrome P450 2C9 genetic polymorphisms and phenytoin-related severe cutaneous adverse reactions in a Thai population Wichittra Tassaneeyakul Napat Prabmeechai Chonlaphat Sukasem Thachanan Kongpan Parinya Konyoung Pansu Chumworathayi Somsak Tiamkao Usanee Khunarkornsiri Kongkiat Kulkantrakorn Niwat Saksit Nontaya Nakkam Patompong Satapornpong Suda Vannaprasaht Alisara Sangviroon Surakameth Mahasirimongkol Nuanjun Wichukchinda Ticha Rerkpattanapipat Wongwiwat Tassaneeyakul Khon Kaen University Faculty of Medicine Integrated Epilepsy Research Group Division of Pharmacogenomics and Personalized Medicine Somdech Phra Debaratana Medical Center (SDMC) Mahidol University Police General Hospital Udonthani Hospital Faculty of Medicine, Thammasat University Thailand Ministry of Public Health Biochemistry, Genetics and Molecular Biology © 2016 Wolters Kluwer Health, Inc. All rights reserved. Background Phenytoin is one of the most common causative drugs of several types of severe cutaneous adverse reactions (SCAR) such as Stevens-Johnson syndrome (SJS), toxic epidermal necrolysis (TEN), and drug reactions with eosinophilia and systemic symptoms (DRESS). Genetic polymorphisms of the human leukocyte antigens (HLA) and cytochromes P450 (CYP) have been proposed as key elements for the susceptibility to phenytoin-related SCAR in certain ethnicities. This study investigated the associations between the genetic polymorphisms of HLA class I and CYP2C9 and phenytoin-related SCAR in a Thai population. Materials and methods Sixty phenytoin-related SCAR (i.e. 39 SJS/TEN and 21 DRESS) and 92 phenytoin-tolerant patients were enrolled in the study. The genotypes of HLA class I and CYP2C9 were determined. Results Six HLA alleles including HLA-A∗33:03, HLAB∗c 38:02, HLA-B∗51:01, HLA-B∗56:02, HLA-B∗c58:01, and HLA-C∗14:02 were significantly associated with phenytoinrelated SJS/TEN, whereas only the HLA-B∗51:01 was significantly associated with phenytoin-related DRESS. The odds ratios of phenytoin-related SJS/TEN in the patients who carried one of these alleles ranged from 4-to 10-fold. The frequencies of patients who carried the HLA-B∗15:02 in the SJS/TEN (12.82%) or the DRESS (9.52%) groups were not significantly different from that of the controls (14.13%). The higher risk of phenytoin-related SJS/TEN was observed in the patients with CYP2C9∗3 (odds ratio=4.30, 95% confidence interval=1.41-13.09, P<0.05). Conclusion Neither SJS/TEN nor DRESS caused by phenytoin was significantly associated with the HLAB∗ 15:02. The CYP2C9∗3 variant was significantly associated with phenytoin-related SJS/TEN, but not DRESS. Certain alleles of HLA, particularly HLA-B∗56:02, were significantly associated with phenytoin-related SCAR in the study population. 2018-12-11T02:26:31Z 2019-03-14T08:04:18Z 2018-12-11T02:26:31Z 2019-03-14T08:04:18Z 2016-01-01 Article Pharmacogenetics and Genomics. Vol.26, No.5 (2016), 225-234 10.1097/FPC.0000000000000211 17446880 17446872 2-s2.0-84959257971 https://repository.li.mahidol.ac.th/handle/123456789/43229 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84959257971&origin=inward |
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Biochemistry, Genetics and Molecular Biology Wichittra Tassaneeyakul Napat Prabmeechai Chonlaphat Sukasem Thachanan Kongpan Parinya Konyoung Pansu Chumworathayi Somsak Tiamkao Usanee Khunarkornsiri Kongkiat Kulkantrakorn Niwat Saksit Nontaya Nakkam Patompong Satapornpong Suda Vannaprasaht Alisara Sangviroon Surakameth Mahasirimongkol Nuanjun Wichukchinda Ticha Rerkpattanapipat Wongwiwat Tassaneeyakul Associations between HLA class i and cytochrome P450 2C9 genetic polymorphisms and phenytoin-related severe cutaneous adverse reactions in a Thai population |
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© 2016 Wolters Kluwer Health, Inc. All rights reserved. Background Phenytoin is one of the most common causative drugs of several types of severe cutaneous adverse reactions (SCAR) such as Stevens-Johnson syndrome (SJS), toxic epidermal necrolysis (TEN), and drug reactions with eosinophilia and systemic symptoms (DRESS). Genetic polymorphisms of the human leukocyte antigens (HLA) and cytochromes P450 (CYP) have been proposed as key elements for the susceptibility to phenytoin-related SCAR in certain ethnicities. This study investigated the associations between the genetic polymorphisms of HLA class I and CYP2C9 and phenytoin-related SCAR in a Thai population. Materials and methods Sixty phenytoin-related SCAR (i.e. 39 SJS/TEN and 21 DRESS) and 92 phenytoin-tolerant patients were enrolled in the study. The genotypes of HLA class I and CYP2C9 were determined. Results Six HLA alleles including HLA-A∗33:03, HLAB∗c 38:02, HLA-B∗51:01, HLA-B∗56:02, HLA-B∗c58:01, and HLA-C∗14:02 were significantly associated with phenytoinrelated SJS/TEN, whereas only the HLA-B∗51:01 was significantly associated with phenytoin-related DRESS. The odds ratios of phenytoin-related SJS/TEN in the patients who carried one of these alleles ranged from 4-to 10-fold. The frequencies of patients who carried the HLA-B∗15:02 in the SJS/TEN (12.82%) or the DRESS (9.52%) groups were not significantly different from that of the controls (14.13%). The higher risk of phenytoin-related SJS/TEN was observed in the patients with CYP2C9∗3 (odds ratio=4.30, 95% confidence interval=1.41-13.09, P<0.05). Conclusion Neither SJS/TEN nor DRESS caused by phenytoin was significantly associated with the HLAB∗ 15:02. The CYP2C9∗3 variant was significantly associated with phenytoin-related SJS/TEN, but not DRESS. Certain alleles of HLA, particularly HLA-B∗56:02, were significantly associated with phenytoin-related SCAR in the study population. |
author2 |
Khon Kaen University |
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Khon Kaen University Wichittra Tassaneeyakul Napat Prabmeechai Chonlaphat Sukasem Thachanan Kongpan Parinya Konyoung Pansu Chumworathayi Somsak Tiamkao Usanee Khunarkornsiri Kongkiat Kulkantrakorn Niwat Saksit Nontaya Nakkam Patompong Satapornpong Suda Vannaprasaht Alisara Sangviroon Surakameth Mahasirimongkol Nuanjun Wichukchinda Ticha Rerkpattanapipat Wongwiwat Tassaneeyakul |
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Article |
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Wichittra Tassaneeyakul Napat Prabmeechai Chonlaphat Sukasem Thachanan Kongpan Parinya Konyoung Pansu Chumworathayi Somsak Tiamkao Usanee Khunarkornsiri Kongkiat Kulkantrakorn Niwat Saksit Nontaya Nakkam Patompong Satapornpong Suda Vannaprasaht Alisara Sangviroon Surakameth Mahasirimongkol Nuanjun Wichukchinda Ticha Rerkpattanapipat Wongwiwat Tassaneeyakul |
author_sort |
Wichittra Tassaneeyakul |
title |
Associations between HLA class i and cytochrome P450 2C9 genetic polymorphisms and phenytoin-related severe cutaneous adverse reactions in a Thai population |
title_short |
Associations between HLA class i and cytochrome P450 2C9 genetic polymorphisms and phenytoin-related severe cutaneous adverse reactions in a Thai population |
title_full |
Associations between HLA class i and cytochrome P450 2C9 genetic polymorphisms and phenytoin-related severe cutaneous adverse reactions in a Thai population |
title_fullStr |
Associations between HLA class i and cytochrome P450 2C9 genetic polymorphisms and phenytoin-related severe cutaneous adverse reactions in a Thai population |
title_full_unstemmed |
Associations between HLA class i and cytochrome P450 2C9 genetic polymorphisms and phenytoin-related severe cutaneous adverse reactions in a Thai population |
title_sort |
associations between hla class i and cytochrome p450 2c9 genetic polymorphisms and phenytoin-related severe cutaneous adverse reactions in a thai population |
publishDate |
2018 |
url |
https://repository.li.mahidol.ac.th/handle/123456789/43229 |
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1763487690538352640 |