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

Medicine (Baltimore)

From the Department of Internal Medicine (YJC, NK, CMS and DHL), Seoul National University Bundang Hospital, Seongnam; Department of Internal Medicine and Liver Research Institute (NK, SO, DHL and HCJ), Seoul National University College of Medicine; and Department of Statistics (WJ, BS), College of Science, Seoul National University, Seoul, South Korea.

Published: May 2016

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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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4902404PMC
http://dx.doi.org/10.1097/MD.0000000000003606DOI Listing

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