Prevalence of Helicobacter pylori Antimicrobial Resistance Among Chilean Patients.


Journal

Archives of medical research
ISSN: 1873-5487
Titre abrégé: Arch Med Res
Pays: United States
ID NLM: 9312706

Informations de publication

Date de publication:
07 2021
Historique:
received: 06 10 2020
revised: 16 12 2020
accepted: 21 01 2021
pubmed: 16 2 2021
medline: 15 12 2021
entrez: 15 2 2021
Statut: ppublish

Résumé

Treatments for Helicobacter pylori (H. pylori) eradication include the use of antibiotics and a proton-pump inhibitor. Antibiotic resistance is a major concern for two drugs: levofloxacin and clarithromycin. The aim was to determine the prevalence of levofloxacin resistance (LevoR) and clarithromycin resistance (ClaR) in an urban population in Santiago, Chile. Gastric mucosa biopsies were obtained for DNA isolation from 143 H. pylori-positive individuals aged 18-80 years. Direct sequencing of the quinolone-resistance determining region (QRDR) of the gyrA gene was used to determine LevoR. ClaR was determined using restriction-fragment length polymorphism or 5'exonuclease assay. The prevalences of LevoR and ClaR were 29 and 27%, respectively. LevoR was higher in women than in men (39 vs. 13%, p <0.001), while no sex difference was observed for ClaR (p = 0.123). The prevalence of LevoR increased with age (p-trend = 0.004) but not for ClaR (p-trend = 0.054). In sex-stratified analyses, both LevoR and ClaR increased with age only among women. Older women (>50 years) had a higher probability to carry LevoR strains as compared to men. The prevalence of dual LevoR and ClaR was 12.6%. The prevalence of ClaR and LevoR is high in Santiago, according to International guidelines that recommend avoiding schemes with antibiotic resistance >15%. Our findings provide evidence to re-evaluate current therapies and guide empirical first- and second-line eradication treatments in Chile.

Sections du résumé

BACKGROUND
Treatments for Helicobacter pylori (H. pylori) eradication include the use of antibiotics and a proton-pump inhibitor. Antibiotic resistance is a major concern for two drugs: levofloxacin and clarithromycin. The aim was to determine the prevalence of levofloxacin resistance (LevoR) and clarithromycin resistance (ClaR) in an urban population in Santiago, Chile.
METHODS
Gastric mucosa biopsies were obtained for DNA isolation from 143 H. pylori-positive individuals aged 18-80 years. Direct sequencing of the quinolone-resistance determining region (QRDR) of the gyrA gene was used to determine LevoR. ClaR was determined using restriction-fragment length polymorphism or 5'exonuclease assay.
RESULTS
The prevalences of LevoR and ClaR were 29 and 27%, respectively. LevoR was higher in women than in men (39 vs. 13%, p <0.001), while no sex difference was observed for ClaR (p = 0.123). The prevalence of LevoR increased with age (p-trend = 0.004) but not for ClaR (p-trend = 0.054). In sex-stratified analyses, both LevoR and ClaR increased with age only among women. Older women (>50 years) had a higher probability to carry LevoR strains as compared to men. The prevalence of dual LevoR and ClaR was 12.6%.
CONCLUSIONS
The prevalence of ClaR and LevoR is high in Santiago, according to International guidelines that recommend avoiding schemes with antibiotic resistance >15%. Our findings provide evidence to re-evaluate current therapies and guide empirical first- and second-line eradication treatments in Chile.

Identifiants

pubmed: 33583603
pii: S0188-4409(21)00034-5
doi: 10.1016/j.arcmed.2021.01.011
pmc: PMC8520490
mid: NIHMS1744750
pii:
doi:

Substances chimiques

Anti-Bacterial Agents 0
Levofloxacin 6GNT3Y5LMF
Clarithromycin H1250JIK0A

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

529-534

Subventions

Organisme : Intramural NIH HHS
ID : ZIA CP000185
Pays : United States

Informations de copyright

Copyright © 2021. Published by Elsevier Inc.

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Auteurs

Patricio González-Hormazábal (P)

Program de Genética Humana, Instituto de Ciencias Biomédicas, Facultad de Medicina, Universidad de Chile. Electronic address: patriciogonzalez@uchile.cl.

Alex Arenas (A)

Hospital Dr. Sótero del Río, Santiago, Chile; Departamento de Gastroenterología, Escuela de Medicina, Pontificia Universidad Católica de Chile.

Carolina Serrano (C)

Departamento de Gastroenterología y Nutrición Pediátrica. Escuela de Medicina, Pontificia Universidad Católica de Chile.

Margarita Pizarro (M)

Departamento de Gastroenterología, Escuela de Medicina, Pontificia Universidad Católica de Chile.

Eduardo Fuentes-López (E)

Departamento de Ciencias de la Salud, Facultad de Medicina. Pontificia Universidad Católica de Chile.

Jorge Arnold (J)

Departamento de Gastroenterología, Escuela de Medicina, Pontificia Universidad Católica de Chile.

Zoltan Berger (Z)

Sección de Gastroenterología, Hospital Clínico de la Universidad de Chile, Santiago, Chile.

Maher Musleh (M)

Departamento de Cirugía, Hospital Clínico de la Universidad de Chile, Santiago, Chile.

Héctor Valladares (H)

Departamento de Cirugía, Hospital Clínico de la Universidad de Chile, Santiago, Chile.

Enrique Lanzarini (E)

Departamento de Cirugía, Hospital Clínico de la Universidad de Chile, Santiago, Chile.

Lilian Jara (L)

Program de Genética Humana, Instituto de Ciencias Biomédicas, Facultad de Medicina, Universidad de Chile.

V Gonzalo Castro (VG)

Program de Genética Humana, Instituto de Ciencias Biomédicas, Facultad de Medicina, Universidad de Chile.

M Constanza Camargo (MC)

Division of Cancer Epidemiology and Genetics, National Cancer Institute, USA.

Arnoldo Riquelme (A)

Departamento de Gastroenterología, Escuela de Medicina, Pontificia Universidad Católica de Chile; Departamento de Ciencias de la Salud, Facultad de Medicina. Pontificia Universidad Católica de Chile.

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