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Association between Helicobacter pylori Infection and Pancreatic Cancer Development: A Meta-Analysis

BACKGROUND: Pancreatic cancer is one of the most troublesome malignancies with dismal prognosis. H. pylori has been recognized as a type I carcinogen. Several studies have evaluated the association between H. pylori infection and pancreatic cancer development, however, the conclusions are inconsiste...

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Autores principales: Xiao, Mingjia, Wang, Yiming, Gao, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3784458/
https://www.ncbi.nlm.nih.gov/pubmed/24086571
http://dx.doi.org/10.1371/journal.pone.0075559
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author Xiao, Mingjia
Wang, Yiming
Gao, Yi
author_facet Xiao, Mingjia
Wang, Yiming
Gao, Yi
author_sort Xiao, Mingjia
collection PubMed
description BACKGROUND: Pancreatic cancer is one of the most troublesome malignancies with dismal prognosis. H. pylori has been recognized as a type I carcinogen. Several studies have evaluated the association between H. pylori infection and pancreatic cancer development, however, the conclusions are inconsistent. METHODS: Literature search was carried out in PubMed, EMBASE, Cochrane Library and CNKI databases to identify eligible researches. We performed overall meta-analysis of all studies included and subgroup analysis based on regional distribution. Quality of the studies (assessed by Newcastle-Ottawa quality assessment scale for case-control studies) and CagA+ strains of H. pylori were taken into consideration, and we conducted additional analyses including high-quality researches and those concerning CagA+ H. pylori respectively. RESULTS: 9 studies involving 3033 subjects (1083 pancreatic cancer cases, 1950 controls) were included. Summary OR and 95%CI of the overall meta-analysis of all included studies were 1.47 and 1.22-1.77, pooled data of the 4 high-quality studies were OR 1.28, 95%CI 1.01-1.63. OR of the 5 studies examined CagA+ strains was 1.42, corresponding 95%CI was 0.79 to 2.57. Summary estimates of subgroup analysis based on regional distribution are as follows, Europe group: OR 1.56, 95%CI 1.15-2.10; East Asia group: OR 2.01, 95%CI 1.33-3.02; North America group: OR 1.17, 95%CI 0.87-1.58. There was not obvious heterogeneity across the 9 studies. No publication bias was detected. CONCLUSION: H. pylori infection is significantly, albeit weakly, associated with pancreatic cancer development. The association is prominent in Europe and East Asia, but not in North America. CagA+ H. pylori strains appear not to be associated with pancreatic cancer. However, more studies, especially prospective studies, are needed to validate our results.
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spelling pubmed-37844582013-10-01 Association between Helicobacter pylori Infection and Pancreatic Cancer Development: A Meta-Analysis Xiao, Mingjia Wang, Yiming Gao, Yi PLoS One Research Article BACKGROUND: Pancreatic cancer is one of the most troublesome malignancies with dismal prognosis. H. pylori has been recognized as a type I carcinogen. Several studies have evaluated the association between H. pylori infection and pancreatic cancer development, however, the conclusions are inconsistent. METHODS: Literature search was carried out in PubMed, EMBASE, Cochrane Library and CNKI databases to identify eligible researches. We performed overall meta-analysis of all studies included and subgroup analysis based on regional distribution. Quality of the studies (assessed by Newcastle-Ottawa quality assessment scale for case-control studies) and CagA+ strains of H. pylori were taken into consideration, and we conducted additional analyses including high-quality researches and those concerning CagA+ H. pylori respectively. RESULTS: 9 studies involving 3033 subjects (1083 pancreatic cancer cases, 1950 controls) were included. Summary OR and 95%CI of the overall meta-analysis of all included studies were 1.47 and 1.22-1.77, pooled data of the 4 high-quality studies were OR 1.28, 95%CI 1.01-1.63. OR of the 5 studies examined CagA+ strains was 1.42, corresponding 95%CI was 0.79 to 2.57. Summary estimates of subgroup analysis based on regional distribution are as follows, Europe group: OR 1.56, 95%CI 1.15-2.10; East Asia group: OR 2.01, 95%CI 1.33-3.02; North America group: OR 1.17, 95%CI 0.87-1.58. There was not obvious heterogeneity across the 9 studies. No publication bias was detected. CONCLUSION: H. pylori infection is significantly, albeit weakly, associated with pancreatic cancer development. The association is prominent in Europe and East Asia, but not in North America. CagA+ H. pylori strains appear not to be associated with pancreatic cancer. However, more studies, especially prospective studies, are needed to validate our results. Public Library of Science 2013-09-26 /pmc/articles/PMC3784458/ /pubmed/24086571 http://dx.doi.org/10.1371/journal.pone.0075559 Text en © 2013 Xiao et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Xiao, Mingjia
Wang, Yiming
Gao, Yi
Association between Helicobacter pylori Infection and Pancreatic Cancer Development: A Meta-Analysis
title Association between Helicobacter pylori Infection and Pancreatic Cancer Development: A Meta-Analysis
title_full Association between Helicobacter pylori Infection and Pancreatic Cancer Development: A Meta-Analysis
title_fullStr Association between Helicobacter pylori Infection and Pancreatic Cancer Development: A Meta-Analysis
title_full_unstemmed Association between Helicobacter pylori Infection and Pancreatic Cancer Development: A Meta-Analysis
title_short Association between Helicobacter pylori Infection and Pancreatic Cancer Development: A Meta-Analysis
title_sort association between helicobacter pylori infection and pancreatic cancer development: a meta-analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3784458/
https://www.ncbi.nlm.nih.gov/pubmed/24086571
http://dx.doi.org/10.1371/journal.pone.0075559
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