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Autoimmune Diseases and Gastric Cancer Risk: A Systematic Review and Meta-Analysis

PURPOSE: Autoimmunity is an alternative etiology of gastric inflammation, the initiating event in the gastric carcinogenic cascade. This mechanism may be an increasingly important cause of gastric cancer with the waning prevalence of its primary etiologic factor, chronic Helicobacter pylori infectio...

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Autores principales: Song, Minkyo, Latorre, Gonzalo, Ivanovic-Zuvic, Danisa, Camargo, M. Constanza, Rabkin, Charles S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Cancer Association 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6639229/
https://www.ncbi.nlm.nih.gov/pubmed/31048663
http://dx.doi.org/10.4143/crt.2019.151
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author Song, Minkyo
Latorre, Gonzalo
Ivanovic-Zuvic, Danisa
Camargo, M. Constanza
Rabkin, Charles S.
author_facet Song, Minkyo
Latorre, Gonzalo
Ivanovic-Zuvic, Danisa
Camargo, M. Constanza
Rabkin, Charles S.
author_sort Song, Minkyo
collection PubMed
description PURPOSE: Autoimmunity is an alternative etiology of gastric inflammation, the initiating event in the gastric carcinogenic cascade. This mechanism may be an increasingly important cause of gastric cancer with the waning prevalence of its primary etiologic factor, chronic Helicobacter pylori infection. MATERIALS AND METHODS: PubMed and EMBASE were searched up to September 2018. Autoimmunity and 96 specific manifestations were considered for associations with gastric cancer risk. Random effects analysis was used to calculate pooled relative risk estimates (RR) and 95% confidence intervals (CI). RESULTS: We found a total of 52 observational studies representing 30 different autoimmune diseases. Overall, the presence of an autoimmune condition was associated with a gastric cancer pooled RR of 1.37 (95% CI, 1.24 to 1.52). Among the 24 autoimmune conditions with two or more independent reports, nine were significantly associated with increased gastric cancer risk: dermatomyositis (RR, 3.69; 95% CI, 1.74 to 7.79), pernicious anemia (RR, 2.84; 95% CI, 2.30 to 3.50), Addison disease (RR, 2.11; 95% CI, 1.26 to 3.53), dermatitis herpetiformis (RR, 1.74; 95% CI, 1.02 to 2.97; n=3), IgG4-related disease (RR, 1.69; 95% CI, 1.00 to 2.87), primary biliary cirrhosis (RR, 1.64; 95% CI, 1.13 to 2.37), diabetes mellitus type 1 (RR, 1.41; 95% CI, 1.20 to 1.67), systemic lupus erythematosus (RR, 1.37; 95% CI, 1.01 to 1.84), and Graves disease (RR, 1.27; 95% CI, 1.06 to 1.52). CONCLUSION: Our analysis documents the wide range of autoimmune diseases associated with gastric cancer. These associations may reflect unreported links between these conditions and autoimmune gastritis. Further studies are warranted to investigate potential causal mechanisms.
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spelling pubmed-66392292019-07-26 Autoimmune Diseases and Gastric Cancer Risk: A Systematic Review and Meta-Analysis Song, Minkyo Latorre, Gonzalo Ivanovic-Zuvic, Danisa Camargo, M. Constanza Rabkin, Charles S. Cancer Res Treat Review Article PURPOSE: Autoimmunity is an alternative etiology of gastric inflammation, the initiating event in the gastric carcinogenic cascade. This mechanism may be an increasingly important cause of gastric cancer with the waning prevalence of its primary etiologic factor, chronic Helicobacter pylori infection. MATERIALS AND METHODS: PubMed and EMBASE were searched up to September 2018. Autoimmunity and 96 specific manifestations were considered for associations with gastric cancer risk. Random effects analysis was used to calculate pooled relative risk estimates (RR) and 95% confidence intervals (CI). RESULTS: We found a total of 52 observational studies representing 30 different autoimmune diseases. Overall, the presence of an autoimmune condition was associated with a gastric cancer pooled RR of 1.37 (95% CI, 1.24 to 1.52). Among the 24 autoimmune conditions with two or more independent reports, nine were significantly associated with increased gastric cancer risk: dermatomyositis (RR, 3.69; 95% CI, 1.74 to 7.79), pernicious anemia (RR, 2.84; 95% CI, 2.30 to 3.50), Addison disease (RR, 2.11; 95% CI, 1.26 to 3.53), dermatitis herpetiformis (RR, 1.74; 95% CI, 1.02 to 2.97; n=3), IgG4-related disease (RR, 1.69; 95% CI, 1.00 to 2.87), primary biliary cirrhosis (RR, 1.64; 95% CI, 1.13 to 2.37), diabetes mellitus type 1 (RR, 1.41; 95% CI, 1.20 to 1.67), systemic lupus erythematosus (RR, 1.37; 95% CI, 1.01 to 1.84), and Graves disease (RR, 1.27; 95% CI, 1.06 to 1.52). CONCLUSION: Our analysis documents the wide range of autoimmune diseases associated with gastric cancer. These associations may reflect unreported links between these conditions and autoimmune gastritis. Further studies are warranted to investigate potential causal mechanisms. Korean Cancer Association 2019-07 2019-05-03 /pmc/articles/PMC6639229/ /pubmed/31048663 http://dx.doi.org/10.4143/crt.2019.151 Text en Copyright © 2019 by the Korean Cancer Association This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Song, Minkyo
Latorre, Gonzalo
Ivanovic-Zuvic, Danisa
Camargo, M. Constanza
Rabkin, Charles S.
Autoimmune Diseases and Gastric Cancer Risk: A Systematic Review and Meta-Analysis
title Autoimmune Diseases and Gastric Cancer Risk: A Systematic Review and Meta-Analysis
title_full Autoimmune Diseases and Gastric Cancer Risk: A Systematic Review and Meta-Analysis
title_fullStr Autoimmune Diseases and Gastric Cancer Risk: A Systematic Review and Meta-Analysis
title_full_unstemmed Autoimmune Diseases and Gastric Cancer Risk: A Systematic Review and Meta-Analysis
title_short Autoimmune Diseases and Gastric Cancer Risk: A Systematic Review and Meta-Analysis
title_sort autoimmune diseases and gastric cancer risk: a systematic review and meta-analysis
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6639229/
https://www.ncbi.nlm.nih.gov/pubmed/31048663
http://dx.doi.org/10.4143/crt.2019.151
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