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Pharmacogenetic Testing for Prevention of Severe Cutaneous Adverse Drug Reactions

Chih‐Jung Chang, Chun‐Bing Chen, Wen‐Hung Chung, Chao Ji, Wen‐Hung Chung

2020Frontiers in Pharmacology57 citationsDOIOpen Access PDF

Abstract

Severe cutaneous adverse reactions (SCAR), such as Stevens-Johnson syndrome (SJS), toxic epidermal necrolysis (TEN), and drug rash with eosinophilia and systemic symptoms (DRESS), are idiosyncratic and unpredictable drug-hypersensitivity reactions with a high-mortality rate ranging from 10% to over 30%, thus causing a major burden on the healthcare system. Recent pharmacogenomic studies have revealed strong associations between SCAR and the genes encoding human-leukocyte antigens (HLAs) or drug-metabolizing enzymes. Some of pharmacogenetic markers have been successfully applied in clinical practice to protect patients from SCAR, such as HLA-B*15:02 and HLA-A*31:01 for new users of carbamazepine, HLA-B*58:01 for allopurinol, and HLA-B*57:01 for abacavir. This article aims to update the current knowledge in the field of pharmacogenomics of drug hypersensitivities or SCAR, and its implementation in the clinical practice.

Topics & Concepts

PharmacogenomicsMedicineToxic epidermal necrolysisAllopurinolAbacavirPharmacogeneticsDrugAdverse effectDermatologyRashCarbamazepineEosinophiliaAdverse drug reactionPharmacologyHuman leukocyte antigenBioinformaticsImmunologyInternal medicineGenotypeEpilepsyAntigenGeneBiologyPsychiatryBiochemistryHepatitis B virusLamivudineVirusDrug-Induced Adverse ReactionsUrticaria and Related ConditionsMast cells and histamine
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