Choi Yoon Jin, Kim Nayoung, Jang Woncheol, Seo Bochang, Oh Sooyeon, Shin Cheol Min, Lee Dong Ho, Jung Hyun Chae
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.
Medicine (Baltimore). 2016 May;95(20):e3606. doi: 10.1097/MD.0000000000003606.
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.
这项全面的横断面研究旨在确定导致胃癌(GC)家族聚集的因素。根据是否有GC一级亲属(GC亲属),对1058例GC患者和1268例对照进行了分别分析。进行了逻辑回归分析,对年龄、性别、童年居住地、吸烟、饮酒、月收入、辛辣食物摄入、幽门螺杆菌状态和宿主细胞因子多态性进行了校正。细胞毒素相关基因A(cagA)阳性是家族史(FH)阳性组GC的一个独特危险因素(比值比[OR],2.39;95%置信区间[CI],1.42 - 4.00),而目前/曾经吸烟者、中度至重度辛辣食物摄入和非B血型与FH阴性组的GC关联更为密切。在FH阳性组中,与有1名GC亲属的组相比,在至少有2名GC亲属的组中饮酒显示出协同致癌作用(1.71对9.58,交互作用P = 0.026),且呈剂量依赖性。在有≥2名GC亲属的受试者中,TGFB1 - 509T/T是GC的一个危险因素(OR 23.74;95% CI 1.37 - 410.91),童年农村居住、饮酒、辛辣食物摄入和cagA阳性也是危险因素。这些结果表明,有FH的受试者在胃癌易感性方面可能是一个异质性群体。特别是,有≥2名GC亲属的受试者应进行包括TGFB1 - 509T/T和饮酒在内的风险分层。