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DC Field | Value | Language |
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dc.contributor.author | Chonlaphat Sukasem | en_US |
dc.contributor.author | Suthida Sririttha | en_US |
dc.contributor.author | Chonlawat Chaichan | en_US |
dc.contributor.author | Thapanat Nakkrut | en_US |
dc.contributor.author | Patompong Satapornpong | en_US |
dc.contributor.author | Kanoot Jaruthamsophon | en_US |
dc.contributor.author | Thawinee Jantararoungtong | en_US |
dc.contributor.author | Napatrupron Koomdee | en_US |
dc.contributor.author | Sadeep Medhasi | en_US |
dc.contributor.author | Sarawut Oo-Puthinan | en_US |
dc.contributor.author | Ticha Rerkpattanapipat | en_US |
dc.contributor.author | Jettanong Klaewsongkram | en_US |
dc.contributor.author | Pawinee Rerknimitr | en_US |
dc.contributor.author | Papapit Tuchinda | en_US |
dc.contributor.author | Leena Chularojanamontri | en_US |
dc.contributor.author | Napatra Tovanabutra | en_US |
dc.contributor.author | Naravut Suvannang | en_US |
dc.contributor.author | Thanyada Rungrotmongkol | en_US |
dc.contributor.author | Surasak Saokaew | en_US |
dc.contributor.author | Wichai Aekplakorn | en_US |
dc.contributor.author | Apichaya Puangpetch | en_US |
dc.date.accessioned | 2022-10-16T07:00:19Z | - |
dc.date.available | 2022-10-16T07:00:19Z | - |
dc.date.issued | 2021-12-01 | en_US |
dc.identifier.issn | 14731150 | en_US |
dc.identifier.issn | 1470269X | en_US |
dc.identifier.other | 2-s2.0-85108814525 | en_US |
dc.identifier.other | 10.1038/s41397-021-00247-3 | en_US |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85108814525&origin=inward | en_US |
dc.identifier.uri | http://cmuir.cmu.ac.th/jspui/handle/6653943832/75503 | - |
dc.description.abstract | 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. | en_US |
dc.subject | Biochemistry, Genetics and Molecular Biology | en_US |
dc.subject | Pharmacology, Toxicology and Pharmaceutics | en_US |
dc.title | Spectrum of cutaneous adverse reactions to aromatic antiepileptic drugs and human leukocyte antigen genotypes in Thai patients and meta-analysis | en_US |
dc.type | Journal | en_US |
article.title.sourcetitle | Pharmacogenomics Journal | en_US |
article.volume | 21 | en_US |
article.stream.affiliations | Ramathibodi Hospital | en_US |
article.stream.affiliations | Siriraj Hospital | en_US |
article.stream.affiliations | Faculty of Tropical Medicine, Mahidol University | en_US |
article.stream.affiliations | University of Phayao | en_US |
article.stream.affiliations | Chulalongkorn University | en_US |
article.stream.affiliations | Faculty of Medicine, Prince of Songkia University | en_US |
article.stream.affiliations | Rangsit University | en_US |
article.stream.affiliations | Naresuan University | en_US |
article.stream.affiliations | Bumrungrad International Hospital | en_US |
article.stream.affiliations | Faculty of Medicine Ramathibodi Hospital, Mahidol University | en_US |
article.stream.affiliations | Mahidol University | en_US |
article.stream.affiliations | Faculty of Medicine, Chulalongkorn University | en_US |
article.stream.affiliations | Chiang Mai University | en_US |
article.stream.affiliations | Triamwitpattana school | en_US |
article.stream.affiliations | The Thai Severe Cutaneous Adverse Drug Reaction (THAI-SCAR) Research Group | en_US |
article.stream.affiliations | Neurological Institute of Thailand | en_US |
Appears in Collections: | CMUL: Journal Articles |
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