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Clinical relevance of pharmacogenetic testing of cytochrome P450 gene (CYP2C19) polymorphisms to personalize the selection of proton pump inhibitors

[Original research] [Clinical Pharmacology] [Pharmacology]
Vladimir Ivanovich Petrov; Anzhelika Viktorovna Ponomareva; Анна Михайловна Доценко; Olga Viktorovna Razvalyaeva; Irina Vyacheslavovna Ivakhnenko;

In the study examined the prevalence of genotypes of the polymorphic 681G/A locus (rs 4244285) and the G636A locus (rs 4986893) of the CYP2C19 gene among the population of the Volgograd region; assess the need for genotyping of this polymorphic locus in clinical practice. Genetic typing of CYP2C19*2 (681G>A), CYP2C19*3 (363G>A) was performed in 183 healthy volunteers aged 18 to 55 years living in Volgograd region. Statistical processing of the results was performed using MS Excel, Statistica 8.0, and GraphPad Prism 5.0. Genotyping of the 681G/A polymorphic locus of the CYP2C19 gene showed that the G/G genotype has the highest prevalence in the population – 76 % of people, the heterozygous G/A variant is observed less frequently – 20.3 % of respondents, 3.3 % had the A/A genotype. Another ratio was found when genotyping the G636A polymorphic locus of the CYP2C19 gene: G/G genotype was 97.82 %, G/A – 1.64 % of respondents, and only 0.54 % of participants had the A/A genotype. Thus, despite the predominance of extensive metabolizers in the population of people living in Volgograd region, there is a need for genotyping of polymorphic locus 681G/A (rs 4244285) and locus G636A (rs 4986893) of CYP2C19 gene in patients with acid-dependent diseases for personalization of PPI selection and its dose.

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Keywords: proton pump inhibitors, genetic polymorphism, CYP2C19, acid-dependent diseases


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