Publication:
Genotyping HLA alleles to predict the development of Severe cutaneous adverse drug reactions (SCARs): state-of-the-art

dc.contributor.authorThawinee Jantararoungtongen_US
dc.contributor.authorTherdpong Temparken_US
dc.contributor.authorNapatrupron Koomdeeen_US
dc.contributor.authorSadeep Medhasien_US
dc.contributor.authorChonlaphat Sukasemen_US
dc.contributor.otherRamathibodi Hospitalen_US
dc.contributor.otherChulalongkorn Universityen_US
dc.contributor.otherBumrungrad International Hospitalen_US
dc.date.accessioned2022-08-04T11:24:10Z
dc.date.available2022-08-04T11:24:10Z
dc.date.issued2021-01-01en_US
dc.description.abstractIntroduction: Pharmacogenomics has great potential in reducing drug-induced severe cutaneous adverse drug reactions (SCARs). Pharmacogenomic studies have revealed an association between HLA genes and SCARs including acute generalized exanthematous pustulosis (AGEP), drug reaction with eosinophilia and systemic symptoms (DRESS), Stevens-Johnson syndrome (SJS), and toxic epidermal necrolysis (TEN). Areas covered: Pharmacogenomics-guided therapy could prevent severe drug hypersensitivity reactions. The US Food and Drug Administration (FDA), Clinical Pharmacogenetics Implementation Consortium (CPIC), and Dutch Pharmacogenetics Working Group (DPWG) provided guidelines in the translation of clinically relevant and evidence-based SCARs pharmacogenomics research into clinical practice. In this review, we intended to summarize the significant HLA alleles associated with SCARs induced by different drugs in different populations. We also summarize the SCARs associated with genetic and non-genetic factors and the cost-effectiveness of screening tests. Expert opinion: The effectiveness of HLA screening on a wider scale in clinical practice requires significant resources, including state-of-the-art laboratory; multidisciplinary team approach and health care provider education and engagement; clinical decision support alert system via electronic medical record (EMR); laboratory standards and quality assurance; evidence of cost-effectiveness; and cost of pharmacogenomics tests and reimbursement.en_US
dc.identifier.citationExpert Opinion on Drug Metabolism and Toxicology. Vol.17, No.9 (2021), 1049-1064en_US
dc.identifier.doi10.1080/17425255.2021.1946514en_US
dc.identifier.issn17447607en_US
dc.identifier.issn17425255en_US
dc.identifier.other2-s2.0-85110221270en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/78976
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85110221270&origin=inwarden_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleGenotyping HLA alleles to predict the development of Severe cutaneous adverse drug reactions (SCARs): state-of-the-arten_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85110221270&origin=inwarden_US

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