Pharmacogenetic Testing for Prevention of Severe Cutaneous Adverse Drug Reactions

Chih Jung Chang, Chun Bing Chen, Shuen Iu Hung, Chao Ji, Wen Hung Chung*

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

50 Scopus citations

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.

Original languageEnglish
Article number969
JournalFrontiers in Pharmacology
Volume11
DOIs
StatePublished - 02 07 2020

Bibliographical note

Publisher Copyright:
© Copyright © 2020 Chang, Chen, Hung, Ji and Chung.

Keywords

  • T cell receptor
  • drug hypersensitivity
  • human-leukocyte antigen
  • pharmacogenetics
  • severe cutaneous adverse reactions

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