Comparison of cytochrome P450 2C9 genotyping methods and implications for the clinical laboratory

Pharmacotherapy. 2004 Jun;24(6):720-6. doi: 10.1592/phco.24.8.720.36074.

Abstract

Study objective: To compare the accuracy, speed, and cost of two methodologies used for genotyping known variants in the cytochrome P450 (CYP) 2C9 metabolizing enzyme gene.

Design: Comparative study.

Setting: University research center.

Samples: Fifteen-milliliter mouthwash samples collected from 253 subjects participating in a warfarin pharmacogenomic study.

Intervention: Genotyping for the isoleucine-to-leucine change at codon 359 (Ile359Leu [*3] polymorphism) was performed by using the Pyrosequencing and polymerase chain reaction (PCR)-restriction fragment length polymorphism (RFLP) methods in all 253 samples. Genotyping for the arginine-to-cysteine change at codon 144 (Arg144Cys [*2] polymorphism) was performed by using Pyrosequencing in all samples and by PCR-RFLP in a random subset of 136 samples.

Measurements and main results: Comparisons of genotyping success rates, time efficiency, and cost analyses were conducted for Pyrosequencing and PCR-RFLP at each variant site. Pyrosequencing and PCR-RFLP produced similar success rates on the first genotyping attempt for the Arg144Cys variant (93.3% vs 90.4%, respectively) and the Ile359Leu variant (83.8% vs 79.1%, respectively). With Pyrosequencing, genotyping 96 samples for either polymorphism could be performed in 1 hour. In contrast, genotyping 96 samples by RFLP took 10 hours for the Arg144Cys variant and 20 hours for the Ile359Leu variant. Total cost/sample for Arg144Cys genotyping was dollars 1.90 with PCR-Pyrosequencing and dollars 3.14 with PCR-RFLP. Total cost/sample for Ile359Leu genotyping was dollars 1.88 with PCR-Pyrosequencing and dollars 10.18 with PCR-RFLP CONCLUSION: Compared with RFLP, genotype determination by Pyrosequencing is a more time-efficient, cost-effective, and robust method for CYP2C9 genotyping. Because of its wide applicability and ease of use, Pyrosequencing is a promising technology for future pharmacogenomic investigations.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Alleles
  • Cost-Benefit Analysis
  • Cytochrome P-450 Enzyme System / genetics*
  • Genotype
  • Humans
  • Laboratories
  • Pharmacogenetics / economics
  • Pharmacogenetics / methods*
  • Polymerase Chain Reaction / economics
  • Polymorphism, Restriction Fragment Length*
  • Sequence Analysis, DNA* / economics
  • Time Factors
  • Warfarin / pharmacology*

Substances

  • Warfarin
  • Cytochrome P-450 Enzyme System