Prolonged clonazepam-induced withdrawal symptoms in an NAT2 ultraslow acetylator

Pharmacogenomics. 2019 Jan;20(2):69-73. doi: 10.2217/pgs-2018-0145. Epub 2018 Dec 6.

Abstract

Clonazepam undergoes nitroreduction to 7-amino-clonazepam via CYP3A4/5, followed by acetylation to 7-acetamido-clonazepam via NAT2 enzyme. While no pharmacological activity is attributed to the metabolites of clonazepam, 7-amino-clonazepam has some affinity for the benzodiazepine receptor as a partial agonist for the gamma aminobutyric acid-A receptor and can compete with clonazepam. Interindividual variability in the incidence of adverse events in patients may, in part, be attributable to differences in clonazepam metabolism. Here, we report on a case of a 70-year-old Caucasian female with insomnia and difficulty weaning off long-term use of clonazepam suggesting that a slow acetylator phenotype contributing to patient's presentation. This hypothesis was confirmed by NAT2 gene sequencing. NAT2 genotyping may play a role in guiding clonazepam therapy.

Keywords: genotype; pharmacogenomics; clonazepam; personalized clonazepam therapy.

Publication types

  • Case Reports

MeSH terms

  • Acetylation / drug effects
  • Aged
  • Arylamine N-Acetyltransferase / genetics*
  • Clonazepam / administration & dosage
  • Clonazepam / adverse effects*
  • Cytochrome P-450 CYP3A / genetics
  • Drug-Related Side Effects and Adverse Reactions / genetics*
  • Drug-Related Side Effects and Adverse Reactions / pathology
  • Female
  • Genotype
  • Humans
  • Polymorphism, Genetic
  • Precision Medicine
  • Substance Withdrawal Syndrome / genetics*
  • Substance Withdrawal Syndrome / pathology

Substances

  • Clonazepam
  • Cytochrome P-450 CYP3A
  • Arylamine N-Acetyltransferase
  • NAT2 protein, human