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Influence of CYP2C19 on Helicobacter pylori eradication in Brazilian patients with functional dyspepsia

Authors :
E F Nardelli
Débora Dreher Nabinger
Guilherme Becker Sander
Rafael do Amaral Cristovam
Daniel Simon
Mirelli Gabardo Klein
G S de Moraes
Carlos Fernando de Magalhães Francesconi
M C Osório
L. Basso da Silva
Felipe Mazzoleni
Tássia Flores Rech
Luiz Edmundo Mazzoleni
Source :
Repositório Institucional da UFRGS, Universidade Federal do Rio Grande do Sul (UFRGS), instacron:UFRGS
Publication Year :
2016
Publisher :
Genetics and Molecular Research, 2016.

Abstract

The aim of this study was to examine the effect of polymorphisms in the cytochrome P450 (CYP) 2C19 gene (CYP2C19) on the Helicobacter pylori eradication rate in Brazilian patients with functional dyspepsia. Adults diagnosed with functional dyspepsia based on the ROME III criteria and infected with H. pylori were recruited to this study. The patients were subjected to gastrointestinal endoscopy and the H. pylori status was defined when both urease test and histopathology results were negative or positive. The patients were treated with proton pump inhibitor-based triple therapy (omeprazole, amoxicillin, and clarithromycin). CYP2C19*2 and CYP2C19*3 were genotyped by polymerase chain reaction-restriction fragment length polymorphism. One hundred and forty-eight patients (81.8% women) with a mean (± SD) age of 46.1 (12.2) years were included in this study. Based on the CYP2C19 genotypes, the patients were classified as homozygous extensive metabolizer (HomEM; 67.6%), heterozygous extensive metabolizer (HetEM; 26.3%), or poor metabolizer (PM; 6.1%). The H. pylori eradication rates in patients with HomEM, HetEM, and PM were 85.0, 89.7, and 100.0% (P = 0.376), respectively. The included study population comprised a high frequency of patients carrying the HomEM genotype. Although the genotypes of CYP2C19 variants were not statistically significant, the results of this study suggest a possible effect of the PM genotype on the efficacy of H. pylori eradication.

Details

ISSN :
16765680
Volume :
15
Database :
OpenAIRE
Journal :
Genetics and Molecular Research
Accession number :
edsair.doi.dedup.....705a207cb3fe9ffba6d0b8d49574516f
Full Text :
https://doi.org/10.4238/gmr.15038734