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Original Article
130 (
4
); 437-443
doi:
10.25259/IJMR_20091304_437

Importance of CYP2C19 genetic polymorphism in the eradication of Helicobacter pylori in north Indians

Department of Biochemistry, Postgraduate Institute of Medical Education & Research, Chandigarh, India
Department of Gastroenterology, Postgraduate Institute of Medical Education & Research, Chandigarh, India

Reprint requests: Dr Krishan K. Kohli, Department of Biochemistry, Postgraduate Institute of Medical Education & Research Chandigarh 160 012, India e-mail: kris_kohli2003@yahoo.com

Licence
This open access article is licensed under Creative Commons Attribution 4.0 International (CC BY 4.0). http://creativecommons.org/licenses/by/4.0

Abstract

Background & objectives:

Genetic polymorphism of CYP2C19 is known to occur with a frequency of 12 per cent in north Indian population. But no study correlated CYP2C19 genetic polymorphism with eradication of Helicobacter pylori in north Indian gastritis patients positive for H. pylori and hence this study.

Methods:

Ninety one consecutive patients positive for H. pylori fulfilling the study criteria were phenotyped and genotyped for CYP2C19. They were given 20 mg omeprazole (OPZ), 750 mg amoxicillin (AMC) and 500 mg tinidazole (TNZ) (bid) for 7 days followed by 20 mg OPZ (qd) for 21 days. Non eradicated extensive metabolizers (EMs) were retreated with 40 mg OPZ (bid) and 500 mg AMC (qid) for 14 days.

Results:

EMs and poor metabolizers (PMs) excreted 4.26 ± 0.34 (95% CI 3.59-4.92) and 0.73 ± 0.05 (95% CI 0.63-0.82) μmol 5-OH-OPZ in 8 h, respectively. After initial therapy, EMs demonstrated 37 per cent (95% CI: 24.5-49.5) and PMs 92 per cent (95% CI: 77-107) eradication of H. pylori. Non eradicated EMs after retreatment demonstrated 90 per cent (95% CI: 79-101) eradication.

Interpretation & conclusions:

This study demonstrated a direct correlation between CYP2C19 genetic polymorphism and H. pylori eradication in north Indian patients with gastritis. Knowing the CYP2C19 phenotype of a patient may help in prescribing optimum dose of proton pump inhibitor to achieve better therapeutic outcome.

Keywords

CYP2C19
Genetic polymorphism
Helicobacter pylori
pharmacogenetics
proton pump inhibitors

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