Publication:
Association of oxcarbazepine-induced cutaneous adverse drug reactions with HLA-B*15:02 Allele

dc.contributor.authorPramote Euasobhonen_US
dc.contributor.authorSukunya Jirachaipitaken_US
dc.contributor.authorSuwanna Chanpraduben_US
dc.contributor.authorPranee Rushatamukayanunten_US
dc.contributor.authorChanin Limwongseen_US
dc.contributor.authorPeter Courtneyen_US
dc.contributor.otherBangkok Metropolitan Administrationen_US
dc.contributor.otherFaculty of Medicine, Siriraj Hospital, Mahidol Universityen_US
dc.contributor.otherRoyal Melbourne Hospitalen_US
dc.date.accessioned2020-08-25T11:21:22Z
dc.date.available2020-08-25T11:21:22Z
dc.date.issued2020-01-01en_US
dc.description.abstract© 2019 Faculty of Medicine Siriraj Hospital, Mahidol University. Objective: Oxcarbazepine (OXC) has similar structure and efficacy to carbamazepine (CBZ), but with fewer side effects. However, there have been only a few reports of serious cutaneous adverse reactions to OXC. HLA-B*15:02's association with cutaneous adverse drug reactions (cADRs) induced by OXC is still inconsistent. This study investigated the incidence of cADRs that were induced by OXC and their association with the HLA-B*15:02 allele in Thais. Methods: A retrospective cohort study of 494 patients receiving oxcarbazepine between January 2012 and January 2018 was undertaken. HLA-B*15:02 testing had been carried out on 79 of the 494 patients. Results: No incidents of serious cutaneous adverse reactions, Stevens-Johnson syndrome (SJS), or toxic epidermal necrolysis (TEN) were found. A 2.4% (12/494) of OXC-related cADRs was determined. Four out of six patients with maculopapular eruptions (MPE) were HLA-B*15:02 positive. Patients who had the allele potentially developed OXC-induced MPE, with an odds ratio of 6.58 (95% CI 1.11-39.15, p=0.040). Only a history of other antiepileptic drug (AED) allergies demonstrated a significant risk factor of OXC-induced MPE. Conclusion: Our research demonstrated that the association between the HLA-B*15:02 allele and MPE induced by OXC was significant. Patients with a history of other AED allergies were also at risk of developing OXC-induced MPE.en_US
dc.identifier.citationSiriraj Medical Journal. Vol.72, No.2 (2020), 174-180en_US
dc.identifier.doi10.33192/Smj.2020.23en_US
dc.identifier.issn22288082en_US
dc.identifier.other2-s2.0-85088626175en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/58299
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85088626175&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleAssociation of oxcarbazepine-induced cutaneous adverse drug reactions with HLA-B*15:02 Alleleen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85088626175&origin=inwarden_US

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