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Spectrum of cutaneous adverse reactions to aromatic antiepileptic drugs and human leukocyte antigen genotypes in Thai patients and meta-analysis
Aromatic antiepileptic drugs (AEDs)-induced cutaneous adverse drug reactions (cADRs) add up to the limited use of the AEDs in the treatment and prevention of seizures. Human leukocyte antigen-B (HLA-B) alleles have been linked to AEDs-induced cADRs. We investigated the association between cADRs (inc...
Autores principales: | , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8602035/ https://www.ncbi.nlm.nih.gov/pubmed/34175889 http://dx.doi.org/10.1038/s41397-021-00247-3 |
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author | Sukasem, Chonlaphat Sririttha, Suthida Chaichan, Chonlawat Nakkrut, Thapanat Satapornpong, Patompong Jaruthamsophon, Kanoot Jantararoungtong, Thawinee Koomdee, Napatrupron Medhasi, Sadeep Oo-Puthinan, Sarawut Rerkpattanapipat, Ticha Klaewsongkram, Jettanong Rerknimitr, Pawinee Tuchinda, Papapit Chularojanamontri, Leena Tovanabutra, Napatra Suvannang, Naravut Rungrotmongkol, Thanyada Saokaew, Surasak Aekplakorn, Wichai Puangpetch, Apichaya |
author_facet | Sukasem, Chonlaphat Sririttha, Suthida Chaichan, Chonlawat Nakkrut, Thapanat Satapornpong, Patompong Jaruthamsophon, Kanoot Jantararoungtong, Thawinee Koomdee, Napatrupron Medhasi, Sadeep Oo-Puthinan, Sarawut Rerkpattanapipat, Ticha Klaewsongkram, Jettanong Rerknimitr, Pawinee Tuchinda, Papapit Chularojanamontri, Leena Tovanabutra, Napatra Suvannang, Naravut Rungrotmongkol, Thanyada Saokaew, Surasak Aekplakorn, Wichai Puangpetch, Apichaya |
author_sort | Sukasem, Chonlaphat |
collection | PubMed |
description | Aromatic antiepileptic drugs (AEDs)-induced cutaneous adverse drug reactions (cADRs) add up to the limited use of the AEDs in the treatment and prevention of seizures. Human leukocyte antigen-B (HLA-B) alleles have been linked to AEDs-induced cADRs. We investigated the association between cADRs (including Stevens–Johnson syndrome; SJS/toxic epidermal necrolysis; TEN, drug reaction with eosinophilia and systemic symptoms; DRESS, and Maculopapular eruption; MPE) caused by AEDs (phenytoin, carbamazepine, lamotrigine, phenobarbital and oxcarbazepine) and HLA-B alleles in Thai population. Through the case-control study, 166 patients with AEDs-induced cADRs, 426 AEDs-tolerant patients (AEDs-tolerant controls), and 470 healthy subjects (Thai population) were collected. The HLA genotypes were detected using the polymerase chain reaction-sequence specific oligonucleotide probe (PCR-SSOP) method. We also performed a meta-analysis with these data and other populations. The carrier rate of HLA-B*15:02 was significantly different between AEDs-induced cADRs group and AEDs-tolerant group (Odds ratio; OR 4.28, 95% Confidence interval; CI 2.64–6.95, p < 0.001), AEDs-induced cADRs group and Thai population (OR 2.15, 95%CI 1.41–3.29, p < 0.001). In meta-analysis showed the strong association HLA-B*15:02 with AEDs-induced cADRs (OR 4.77, 95%CI 1.79–12.73, p < 0.001). Furthermore, HLA-B*15:02 was associated with SJS/TEN induced by AEDs (OR 10.28, 95%CI 6.50–16.28, p < 0.001) Phenytoin (OR 4.12, 95%CI 1.77–9.59, p = 0.001) and carbamazepine (OR 137.69, 95%CI 50.97–371.98, p < 0.001). This study demonstrated that genetic association for AEDs-induced cADRs was phenotype-specific. A strong association between HLA-B*15:02 and AEDs-induced SJS/TEN was demonstrated with an OR of 10.79 (95%CI 5.50–21.16, p < 0.001) when compared with AEDs-tolerant group. On the other hand, the carrier rates of HLA-B*08:01, HLA-B*13:01, and HLA-B*56:02 were significantly higher in the DRESS group compared with the AEDs-tolerant group (p = 0.029, 0.007, and 0.017, respectively). The HLA-B*15:02 allele may represent a risk factor for AEDs-induced cADRs. |
format | Online Article Text |
id | pubmed-8602035 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-86020352021-12-02 Spectrum of cutaneous adverse reactions to aromatic antiepileptic drugs and human leukocyte antigen genotypes in Thai patients and meta-analysis Sukasem, Chonlaphat Sririttha, Suthida Chaichan, Chonlawat Nakkrut, Thapanat Satapornpong, Patompong Jaruthamsophon, Kanoot Jantararoungtong, Thawinee Koomdee, Napatrupron Medhasi, Sadeep Oo-Puthinan, Sarawut Rerkpattanapipat, Ticha Klaewsongkram, Jettanong Rerknimitr, Pawinee Tuchinda, Papapit Chularojanamontri, Leena Tovanabutra, Napatra Suvannang, Naravut Rungrotmongkol, Thanyada Saokaew, Surasak Aekplakorn, Wichai Puangpetch, Apichaya Pharmacogenomics J Article Aromatic antiepileptic drugs (AEDs)-induced cutaneous adverse drug reactions (cADRs) add up to the limited use of the AEDs in the treatment and prevention of seizures. Human leukocyte antigen-B (HLA-B) alleles have been linked to AEDs-induced cADRs. We investigated the association between cADRs (including Stevens–Johnson syndrome; SJS/toxic epidermal necrolysis; TEN, drug reaction with eosinophilia and systemic symptoms; DRESS, and Maculopapular eruption; MPE) caused by AEDs (phenytoin, carbamazepine, lamotrigine, phenobarbital and oxcarbazepine) and HLA-B alleles in Thai population. Through the case-control study, 166 patients with AEDs-induced cADRs, 426 AEDs-tolerant patients (AEDs-tolerant controls), and 470 healthy subjects (Thai population) were collected. The HLA genotypes were detected using the polymerase chain reaction-sequence specific oligonucleotide probe (PCR-SSOP) method. We also performed a meta-analysis with these data and other populations. The carrier rate of HLA-B*15:02 was significantly different between AEDs-induced cADRs group and AEDs-tolerant group (Odds ratio; OR 4.28, 95% Confidence interval; CI 2.64–6.95, p < 0.001), AEDs-induced cADRs group and Thai population (OR 2.15, 95%CI 1.41–3.29, p < 0.001). In meta-analysis showed the strong association HLA-B*15:02 with AEDs-induced cADRs (OR 4.77, 95%CI 1.79–12.73, p < 0.001). Furthermore, HLA-B*15:02 was associated with SJS/TEN induced by AEDs (OR 10.28, 95%CI 6.50–16.28, p < 0.001) Phenytoin (OR 4.12, 95%CI 1.77–9.59, p = 0.001) and carbamazepine (OR 137.69, 95%CI 50.97–371.98, p < 0.001). This study demonstrated that genetic association for AEDs-induced cADRs was phenotype-specific. A strong association between HLA-B*15:02 and AEDs-induced SJS/TEN was demonstrated with an OR of 10.79 (95%CI 5.50–21.16, p < 0.001) when compared with AEDs-tolerant group. On the other hand, the carrier rates of HLA-B*08:01, HLA-B*13:01, and HLA-B*56:02 were significantly higher in the DRESS group compared with the AEDs-tolerant group (p = 0.029, 0.007, and 0.017, respectively). The HLA-B*15:02 allele may represent a risk factor for AEDs-induced cADRs. Nature Publishing Group UK 2021-06-26 2021 /pmc/articles/PMC8602035/ /pubmed/34175889 http://dx.doi.org/10.1038/s41397-021-00247-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Sukasem, Chonlaphat Sririttha, Suthida Chaichan, Chonlawat Nakkrut, Thapanat Satapornpong, Patompong Jaruthamsophon, Kanoot Jantararoungtong, Thawinee Koomdee, Napatrupron Medhasi, Sadeep Oo-Puthinan, Sarawut Rerkpattanapipat, Ticha Klaewsongkram, Jettanong Rerknimitr, Pawinee Tuchinda, Papapit Chularojanamontri, Leena Tovanabutra, Napatra Suvannang, Naravut Rungrotmongkol, Thanyada Saokaew, Surasak Aekplakorn, Wichai Puangpetch, Apichaya Spectrum of cutaneous adverse reactions to aromatic antiepileptic drugs and human leukocyte antigen genotypes in Thai patients and meta-analysis |
title | Spectrum of cutaneous adverse reactions to aromatic antiepileptic drugs and human leukocyte antigen genotypes in Thai patients and meta-analysis |
title_full | Spectrum of cutaneous adverse reactions to aromatic antiepileptic drugs and human leukocyte antigen genotypes in Thai patients and meta-analysis |
title_fullStr | Spectrum of cutaneous adverse reactions to aromatic antiepileptic drugs and human leukocyte antigen genotypes in Thai patients and meta-analysis |
title_full_unstemmed | Spectrum of cutaneous adverse reactions to aromatic antiepileptic drugs and human leukocyte antigen genotypes in Thai patients and meta-analysis |
title_short | Spectrum of cutaneous adverse reactions to aromatic antiepileptic drugs and human leukocyte antigen genotypes in Thai patients and meta-analysis |
title_sort | spectrum of cutaneous adverse reactions to aromatic antiepileptic drugs and human leukocyte antigen genotypes in thai patients and meta-analysis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8602035/ https://www.ncbi.nlm.nih.gov/pubmed/34175889 http://dx.doi.org/10.1038/s41397-021-00247-3 |
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