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Familial Clustering of Gastric Cancer: A Retrospective Study Based on the Number of First-Degree Relatives

This comprehensive cross-sectional study aimed to identify factors contributing to familial aggregation of gastric cancer (GC). A total of 1058 GC patients and 1268 controls were analyzed separately according to the presence or absence of a first-degree relative of GC (GC-relative). Logistic regress...

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Autores principales: Choi, Yoon Jin, Kim, Nayoung, Jang, Woncheol, Seo, Bochang, Oh, Sooyeon, Shin, Cheol Min, Lee, Dong Ho, Jung, Hyun Chae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4902404/
https://www.ncbi.nlm.nih.gov/pubmed/27196462
http://dx.doi.org/10.1097/MD.0000000000003606
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author Choi, Yoon Jin
Kim, Nayoung
Jang, Woncheol
Seo, Bochang
Oh, Sooyeon
Shin, Cheol Min
Lee, Dong Ho
Jung, Hyun Chae
author_facet Choi, Yoon Jin
Kim, Nayoung
Jang, Woncheol
Seo, Bochang
Oh, Sooyeon
Shin, Cheol Min
Lee, Dong Ho
Jung, Hyun Chae
author_sort Choi, Yoon Jin
collection PubMed
description This comprehensive cross-sectional study aimed to identify factors contributing to familial aggregation of gastric cancer (GC). A total of 1058 GC patients and 1268 controls were analyzed separately according to the presence or absence of a first-degree relative of GC (GC-relative). Logistic regression analysis adjusted for age, gender, residence during childhood, smoking, alcohol intake, monthly income, spicy food ingestion, Helicobacter pylori status and host cytokine polymorphisms was performed. Cytotoxin-associated gene A (cagA) positivity was a distinctive risk factor for GC in the family history (FH)-positive group (odds ratio [OR], 2.39; 95% confidence interval [CI], 1.42–4.00), while current/ex-smoker, moderate to strong spicy food ingestion, and non-B blood types were more closely associated with GC in the FH-negative group. Among the FH-positive group, alcohol consumption showed a synergistic carcinogenic effect in the at least 2 GC-relatives group compared to the 1 GC-relative group (1.71 vs. 9.58, P for interaction = 0.026), and this was dose-dependent. In the subjects with ≥2 GC-relatives, TGFB1-509T/T was a risk factor for GC (OR 23.74; 95% CI 1.37–410.91), as were rural residency in childhood, alcohol consumption, spicy food ingestion, and cagA positivity. These results suggest that subjects with FH may be a heterogeneous group in terms of gastric cancer susceptibility. Especially, subjects with ≥2 GC-relatives should undergo risk stratification including TGFB1-509T/T and alcohol consumption.
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spelling pubmed-49024042016-06-23 Familial Clustering of Gastric Cancer: A Retrospective Study Based on the Number of First-Degree Relatives Choi, Yoon Jin Kim, Nayoung Jang, Woncheol Seo, Bochang Oh, Sooyeon Shin, Cheol Min Lee, Dong Ho Jung, Hyun Chae Medicine (Baltimore) 4500 This comprehensive cross-sectional study aimed to identify factors contributing to familial aggregation of gastric cancer (GC). A total of 1058 GC patients and 1268 controls were analyzed separately according to the presence or absence of a first-degree relative of GC (GC-relative). Logistic regression analysis adjusted for age, gender, residence during childhood, smoking, alcohol intake, monthly income, spicy food ingestion, Helicobacter pylori status and host cytokine polymorphisms was performed. Cytotoxin-associated gene A (cagA) positivity was a distinctive risk factor for GC in the family history (FH)-positive group (odds ratio [OR], 2.39; 95% confidence interval [CI], 1.42–4.00), while current/ex-smoker, moderate to strong spicy food ingestion, and non-B blood types were more closely associated with GC in the FH-negative group. Among the FH-positive group, alcohol consumption showed a synergistic carcinogenic effect in the at least 2 GC-relatives group compared to the 1 GC-relative group (1.71 vs. 9.58, P for interaction = 0.026), and this was dose-dependent. In the subjects with ≥2 GC-relatives, TGFB1-509T/T was a risk factor for GC (OR 23.74; 95% CI 1.37–410.91), as were rural residency in childhood, alcohol consumption, spicy food ingestion, and cagA positivity. These results suggest that subjects with FH may be a heterogeneous group in terms of gastric cancer susceptibility. Especially, subjects with ≥2 GC-relatives should undergo risk stratification including TGFB1-509T/T and alcohol consumption. Wolters Kluwer Health 2016-05-20 /pmc/articles/PMC4902404/ /pubmed/27196462 http://dx.doi.org/10.1097/MD.0000000000003606 Text en Copyright © 2016 Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. http://creativecommons.org/licenses/by-nc-sa/4.0
spellingShingle 4500
Choi, Yoon Jin
Kim, Nayoung
Jang, Woncheol
Seo, Bochang
Oh, Sooyeon
Shin, Cheol Min
Lee, Dong Ho
Jung, Hyun Chae
Familial Clustering of Gastric Cancer: A Retrospective Study Based on the Number of First-Degree Relatives
title Familial Clustering of Gastric Cancer: A Retrospective Study Based on the Number of First-Degree Relatives
title_full Familial Clustering of Gastric Cancer: A Retrospective Study Based on the Number of First-Degree Relatives
title_fullStr Familial Clustering of Gastric Cancer: A Retrospective Study Based on the Number of First-Degree Relatives
title_full_unstemmed Familial Clustering of Gastric Cancer: A Retrospective Study Based on the Number of First-Degree Relatives
title_short Familial Clustering of Gastric Cancer: A Retrospective Study Based on the Number of First-Degree Relatives
title_sort familial clustering of gastric cancer: a retrospective study based on the number of first-degree relatives
topic 4500
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4902404/
https://www.ncbi.nlm.nih.gov/pubmed/27196462
http://dx.doi.org/10.1097/MD.0000000000003606
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