An analysis of allele, genotype and phenotype frequencies, actionable pharmacogenomic (PGx) variants and phenoconversion in 5408 Australian patients genotyped for CYP2D6, CYP2C19, CYP2C9 and VKORC1 genes

J Neural Transm (Vienna). 2019 Jan;126(1):5-18. doi: 10.1007/s00702-018-1922-0. Epub 2018 Sep 6.

Abstract

Common polymorphisms in the genes encoding CYP2D6, CYP2C19, CYP2C9 and VKORC1 enzymes have an important role in predicting the occurrence of adverse effects and the efficacy of substrate medications. Drug-induced changes to the enzyme's phenotype, a process called phenoconversion, comprise another important factor contributing to interindividual variability in drug response. To date, there is lack of data on the frequency of these common polymorphisms and phenoconversion in the pan-ethnic Australian population. The aim of this study was to (1) describe allele, genotype and phenotype frequencies for CYP2D6, CYP2C19, CYP2C9 and VKORC1 enzymes in the pan-ethnic Australian population and (2) evaluate the frequency of actionable pharmacogenomic (PGx) variants and phenoconversion. Frequencies were calculated using the records of 5408 Australian patients (obtained from myDNA's propriety database), who were consecutively tested with the DNAdose PGx test which included the CYP2D6, CYP2C19, CYP2C9 and VKORC1 genes. In 2509 patients with listed medications at the time of testing, phenoconversion frequencies were calculated for CYP2D6, CYP2C19 and CYP2C9 enzymes. Allele, genotype and phenotype frequencies in our Australian patients correlated with a Caucasian population. Approximately 96% of patients had at least one actionable PGx variant. A five-fold increase in the frequency of poor metabolisers (PMs) for CYP2D6 and CYP2C19 was predicted by phenoconversion. Our study results indicate a high frequency of actionable PGx variants in our Australian population. With the addition of drug-induced phenoconversion, our results provide further support for the utilisation of PGx testing in clinical practice as another tool assisting prescribers in the application of personalised medicine.

Keywords: Actionable; CYP2C19; CYP2C9; CYP2D6; Pharmacogenomic; Phenoconversion; VKORC1.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Australia
  • Child
  • Child, Preschool
  • Cytochrome P-450 CYP2C19* / drug effects
  • Cytochrome P-450 CYP2C19* / genetics
  • Cytochrome P-450 CYP2C9* / drug effects
  • Cytochrome P-450 CYP2C9* / genetics
  • Cytochrome P-450 CYP2D6* / drug effects
  • Cytochrome P-450 CYP2D6* / genetics
  • Drug Prescriptions
  • Drug-Related Side Effects and Adverse Reactions / enzymology*
  • Drug-Related Side Effects and Adverse Reactions / genetics*
  • Female
  • Genotype
  • Humans
  • Infant
  • Male
  • Middle Aged
  • Pharmacogenomic Variants*
  • Phenotype
  • Polymorphism, Genetic
  • Precision Medicine*
  • Vitamin K Epoxide Reductases* / drug effects
  • Vitamin K Epoxide Reductases* / genetics
  • Young Adult

Substances

  • Cytochrome P-450 CYP2C9
  • CYP2C19 protein, human
  • Cytochrome P-450 CYP2C19
  • Cytochrome P-450 CYP2D6
  • VKORC1 protein, human
  • Vitamin K Epoxide Reductases