Pharmacogenetics of opioid response

Clin Pharmacol Ther. 2015 Feb;97(2):125-7. doi: 10.1002/cpt.23. Epub 2014 Dec 9.

Abstract

For opioids requiring CYP2D6 O-demethylation to active metabolites, poor metabolizers have reduced metabolite formation and minimal pain reduction. Clinically, this has only reliably been shown for tramadol. Ultra-rapid metabolizers have an increased risk of toxicity especially for codeine. ABCB1 genetics show no consistent findings. In Asian populations, the high OPRM1 118A>G frequency associates with higher opioid dosage requirements. Clinical translation of opioid genetics is premature because many important pain and addiction phenotype factors contribute.

MeSH terms

  • Analgesics, Opioid / pharmacokinetics
  • Analgesics, Opioid / therapeutic use*
  • Cytochrome P-450 Enzyme System / genetics*
  • Glucuronosyltransferase / genetics*
  • Humans
  • Pain / drug therapy*
  • Pain / genetics

Substances

  • Analgesics, Opioid
  • Cytochrome P-450 Enzyme System
  • Glucuronosyltransferase