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Early-Life Family Structure and Microbially Induced Cancer Risk

BACKGROUND: Cancer may follow exposure to an environmental agent after many decades. The bacterium Helicobacter pylori, known to be acquired early in life, increases risk for gastric adenocarcinoma, but other factors are also important. In this study, we considered whether early-life family structur...

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Autores principales: Blaser, Martin J, Nomura, Abraham, Lee, James, Stemmerman, Grant N, Perez-Perez, Guillermo I
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1769414/
https://www.ncbi.nlm.nih.gov/pubmed/17227131
http://dx.doi.org/10.1371/journal.pmed.0040007
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author Blaser, Martin J
Nomura, Abraham
Lee, James
Stemmerman, Grant N
Perez-Perez, Guillermo I
author_facet Blaser, Martin J
Nomura, Abraham
Lee, James
Stemmerman, Grant N
Perez-Perez, Guillermo I
author_sort Blaser, Martin J
collection PubMed
description BACKGROUND: Cancer may follow exposure to an environmental agent after many decades. The bacterium Helicobacter pylori, known to be acquired early in life, increases risk for gastric adenocarcinoma, but other factors are also important. In this study, we considered whether early-life family structure affects the risk of later developing gastric cancer among H. pylori (+) men. METHODS AND FINDINGS: We examined a long-term cohort of Japanese-American men followed for 28 y, and performed a nested case-control study among those carrying H. pylori or the subset carrying the most virulent cagA(+) H. pylori strains to address whether family structure predicted cancer development. We found that among the men who were H. pylori(+) and/or cagA (+) (it is possible to be cagA(+) and H. pylori (−) if the H. pylori test is falsely negative), belonging to a large sibship or higher birth order was associated with a significantly increased risk of developing gastric adenocarcinoma late in life. For those with cagA(+) strains, the risk of developing gastric cancer was more than twice as high (odds ratio 2.2; 95% confidence interval 1.2–4.0) among those in a sibship of seven or more individuals than in a sibship of between one and three persons. CONCLUSIONS: These results provide evidence that early-life social environment plays a significant role in risk of microbially induced malignancies expressing five to eight decades later, and these findings lead to new models to explain these interactions.
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spelling pubmed-17694142007-02-09 Early-Life Family Structure and Microbially Induced Cancer Risk Blaser, Martin J Nomura, Abraham Lee, James Stemmerman, Grant N Perez-Perez, Guillermo I PLoS Med Research Article BACKGROUND: Cancer may follow exposure to an environmental agent after many decades. The bacterium Helicobacter pylori, known to be acquired early in life, increases risk for gastric adenocarcinoma, but other factors are also important. In this study, we considered whether early-life family structure affects the risk of later developing gastric cancer among H. pylori (+) men. METHODS AND FINDINGS: We examined a long-term cohort of Japanese-American men followed for 28 y, and performed a nested case-control study among those carrying H. pylori or the subset carrying the most virulent cagA(+) H. pylori strains to address whether family structure predicted cancer development. We found that among the men who were H. pylori(+) and/or cagA (+) (it is possible to be cagA(+) and H. pylori (−) if the H. pylori test is falsely negative), belonging to a large sibship or higher birth order was associated with a significantly increased risk of developing gastric adenocarcinoma late in life. For those with cagA(+) strains, the risk of developing gastric cancer was more than twice as high (odds ratio 2.2; 95% confidence interval 1.2–4.0) among those in a sibship of seven or more individuals than in a sibship of between one and three persons. CONCLUSIONS: These results provide evidence that early-life social environment plays a significant role in risk of microbially induced malignancies expressing five to eight decades later, and these findings lead to new models to explain these interactions. Public Library of Science 2007-01 2007-01-16 /pmc/articles/PMC1769414/ /pubmed/17227131 http://dx.doi.org/10.1371/journal.pmed.0040007 Text en © 2007 Blaser 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
Blaser, Martin J
Nomura, Abraham
Lee, James
Stemmerman, Grant N
Perez-Perez, Guillermo I
Early-Life Family Structure and Microbially Induced Cancer Risk
title Early-Life Family Structure and Microbially Induced Cancer Risk
title_full Early-Life Family Structure and Microbially Induced Cancer Risk
title_fullStr Early-Life Family Structure and Microbially Induced Cancer Risk
title_full_unstemmed Early-Life Family Structure and Microbially Induced Cancer Risk
title_short Early-Life Family Structure and Microbially Induced Cancer Risk
title_sort early-life family structure and microbially induced cancer risk
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1769414/
https://www.ncbi.nlm.nih.gov/pubmed/17227131
http://dx.doi.org/10.1371/journal.pmed.0040007
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