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The distribution of cagA and dupA genes in Helicobacter pylori strains in Kurdistan region, northern Iraq
BACKGROUND AND OBJECTIVES: Helicobacter pylori is a Gram negative bacteria that causes peptic ulceration and gastric adenocarcinoma. H pylori virulence factors, such as cagA and dupA, are important to study in populations as they contribute to disease risk. This study aimed to look at the distributi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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King Faisal Specialist Hospital and Research Centre
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6078529/ https://www.ncbi.nlm.nih.gov/pubmed/23793434 http://dx.doi.org/10.5144/0256-4947.2013.290 |
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author | Salih, Azad M. Goreal, Amer Hussein, Nawfal R. Abdullah, Shahla M. Hawrami, Khidir Assafi, Mahde |
author_facet | Salih, Azad M. Goreal, Amer Hussein, Nawfal R. Abdullah, Shahla M. Hawrami, Khidir Assafi, Mahde |
author_sort | Salih, Azad M. |
collection | PubMed |
description | BACKGROUND AND OBJECTIVES: Helicobacter pylori is a Gram negative bacteria that causes peptic ulceration and gastric adenocarcinoma. H pylori virulence factors, such as cagA and dupA, are important to study in populations as they contribute to disease risk. This study aimed to look at the distribution of the cagA and dupA genes in H pylori strains isolated from patients suffering from gastroduodenal diseases in Kurdistan region, Iraq. DESIGN AND SETTINGS: A cross-sectional study conducted between June 2011 and January 2012. Biopsies were collected from the Endoscopy Department in Duhok and Sulaimania hospitals, Kurdistan region, northern Iraq. PATIENTS AND METHODS: Upper gastrointestinal (GI) endoscopy examination was performed and 4 gastric biopsies (2 from the antrum and 2 from the corpus) were obtained from 204 patients. H pylori positivity was examined by CLO test; then the association between disease status and virulence factors was assessed by polymerase chain reaction. RESULTS: 154 (75%) of our samples were found to be H pylori + by CLO test. Endoscopic diagnoses for those who were positive were as follows: peptic ulcer disease (PUD) including duodenal ulcer, 45; gastric ulcer, 23; and no ulcer (NPUD), 86. The overall prevalence rates of cagA and dupA were 72.7% and 18.8%, respectively. While a significant association between cagA and PUD was observed (P ≤ .017; OR=0.4; CI=0.18–0.85), no relationship between dupA and PUD could be seen. CONCLUSION: These data suggested that the presence of cagA may be a predictor of clinical outcome in Kurdistan region, northern Iraq. |
format | Online Article Text |
id | pubmed-6078529 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | King Faisal Specialist Hospital and Research Centre |
record_format | MEDLINE/PubMed |
spelling | pubmed-60785292018-09-21 The distribution of cagA and dupA genes in Helicobacter pylori strains in Kurdistan region, northern Iraq Salih, Azad M. Goreal, Amer Hussein, Nawfal R. Abdullah, Shahla M. Hawrami, Khidir Assafi, Mahde Ann Saudi Med Brief Report BACKGROUND AND OBJECTIVES: Helicobacter pylori is a Gram negative bacteria that causes peptic ulceration and gastric adenocarcinoma. H pylori virulence factors, such as cagA and dupA, are important to study in populations as they contribute to disease risk. This study aimed to look at the distribution of the cagA and dupA genes in H pylori strains isolated from patients suffering from gastroduodenal diseases in Kurdistan region, Iraq. DESIGN AND SETTINGS: A cross-sectional study conducted between June 2011 and January 2012. Biopsies were collected from the Endoscopy Department in Duhok and Sulaimania hospitals, Kurdistan region, northern Iraq. PATIENTS AND METHODS: Upper gastrointestinal (GI) endoscopy examination was performed and 4 gastric biopsies (2 from the antrum and 2 from the corpus) were obtained from 204 patients. H pylori positivity was examined by CLO test; then the association between disease status and virulence factors was assessed by polymerase chain reaction. RESULTS: 154 (75%) of our samples were found to be H pylori + by CLO test. Endoscopic diagnoses for those who were positive were as follows: peptic ulcer disease (PUD) including duodenal ulcer, 45; gastric ulcer, 23; and no ulcer (NPUD), 86. The overall prevalence rates of cagA and dupA were 72.7% and 18.8%, respectively. While a significant association between cagA and PUD was observed (P ≤ .017; OR=0.4; CI=0.18–0.85), no relationship between dupA and PUD could be seen. CONCLUSION: These data suggested that the presence of cagA may be a predictor of clinical outcome in Kurdistan region, northern Iraq. King Faisal Specialist Hospital and Research Centre 2013 /pmc/articles/PMC6078529/ /pubmed/23793434 http://dx.doi.org/10.5144/0256-4947.2013.290 Text en Copyright © 2013, Annals of Saudi Medicine This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Brief Report Salih, Azad M. Goreal, Amer Hussein, Nawfal R. Abdullah, Shahla M. Hawrami, Khidir Assafi, Mahde The distribution of cagA and dupA genes in Helicobacter pylori strains in Kurdistan region, northern Iraq |
title | The distribution of cagA and dupA genes in Helicobacter pylori strains in Kurdistan region, northern Iraq |
title_full | The distribution of cagA and dupA genes in Helicobacter pylori strains in Kurdistan region, northern Iraq |
title_fullStr | The distribution of cagA and dupA genes in Helicobacter pylori strains in Kurdistan region, northern Iraq |
title_full_unstemmed | The distribution of cagA and dupA genes in Helicobacter pylori strains in Kurdistan region, northern Iraq |
title_short | The distribution of cagA and dupA genes in Helicobacter pylori strains in Kurdistan region, northern Iraq |
title_sort | distribution of caga and dupa genes in helicobacter pylori strains in kurdistan region, northern iraq |
topic | Brief Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6078529/ https://www.ncbi.nlm.nih.gov/pubmed/23793434 http://dx.doi.org/10.5144/0256-4947.2013.290 |
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