[HIGH FREQUENCY OF CYP2C19 ULTRARAPID METABOLIZERS IN RUSSIAN PATIENTS WITH PEPTIC ULCER]

Eksp Klin Gastroenterol. 2015:(6):11-5.
[Article in Russian]

Abstract

Introduction: The main enzyme responsible for metabolism of proton pump inhibitors (PPI) is cytochrome P-4502C19 (CYP2C19). Among all CYP2C19 polymorphisms ulrarapid CYP2C19*17 allele plays an important role in clinical practice as in CYP2C19*17 allele carriers acid suppression achieved with PPI including eradication regimens may be insufficient.

The aim of the study: To find the frequency of CYP2C19 ultrarapid metabolizers in Russian patients with peptic ulcer

Methods: We retrospectively reviewed the results of pharmacogenetic tests of 971 Russian patients with endoscopically and histologically proven ulcers, 428 male (44%) and 543 female (56%). The mean age was 44.6 ± 11.9 years (range 15-88 years). DNA was extracted from EDTA whole blood samples (10 mL). The polymorphisms CYP2C19 *2, *3 *17 were evaluated using real-time polymerase chain reaction (RT-PCR).

Results: We found that among 971 peptic ulcer patients ultrarapid metabolizers (CYP2C19*1/*17, CYP2C19*17/*17) were the most frequent genotype--39.75%. Extensive metabolizers with CYP2C19*1/*1 genotype were less frequent--32.65%. Frequency of poor and intermediate metabolizers was found to be 1.5% and 25.85% respectively. We were the first to investigate CYP2C19*17 allele frequency in Russian patients with peptic ulcer which was found to be 27.4%.

Conclusion: High frequency of CYP2C19 ultrarapid metabolizers in Russian patients with peptic ulcer may be associated with insufficient response to proton pump inhibitors.

MeSH terms

  • Adult
  • Cytochrome P-450 CYP2C19* / genetics
  • Cytochrome P-450 CYP2C19* / metabolism
  • Female
  • Gene Frequency*
  • Genotype*
  • Humans
  • Male
  • Middle Aged
  • Moscow
  • Peptic Ulcer* / drug therapy
  • Peptic Ulcer* / enzymology
  • Peptic Ulcer* / genetics
  • Polymorphism, Genetic*
  • Proton Pump Inhibitors* / administration & dosage
  • Proton Pump Inhibitors* / pharmacokinetics
  • Retrospective Studies

Substances

  • Proton Pump Inhibitors
  • CYP2C19 protein, human
  • Cytochrome P-450 CYP2C19