Infections and Immunoepidemiology Branch, Division of Cancer Epidemiology and Genetics, Department of Health and Human Services, National Cancer Institute, National Institutes of Health, 9609 Medical Center Drive, Bethesda, MD, 20892-9776, USA.
Department of Public Health Solutions, National Institute for Health and Welfare, Helsinki, Finland.
Gastric Cancer. 2018 Sep;21(5):729-737. doi: 10.1007/s10120-018-0807-0. Epub 2018 Feb 17.
Family history may inform risks of gastric cancer and preneoplastic lesions.
We examined associations with history of cancer in first-degree relatives for 307 incident gastric cancer cases among 20,720 male smokers in a prospective study in Finland. Cox regression was used to calculate gastric cancer hazard ratios (HR) and 95% confidence intervals (95% CI). Logistic regression was used to estimate odds ratios (OR) and 95% CIs for low serum pepsinogen, a marker of gastric atrophy.
Gastric cancer risk was associated with gastric cancer history in first-degree relatives overall (HR 1.56, 95% CI 1.15-2.12), in fathers (HR 1.67, 95% CI 1.09-2.55) and in siblings (HR 2.05, 95% CI 1.25-3.38). Associations were significant for noncardia (HR 1.83, 95% CI 1.30-2.57) but not cardia (HR 0.93, 95% CI 0.46-1.87) cancers, and marginal for both intestinal-(HR 1.53, 95% CI 0.92-2.55) and diffuse-type (HR 1.47, 95% CI 0.72-3.03) histologies. Family history of other cancer types was not associated with gastric cancer risk. Family history of gastric cancer was associated with low pepsinogen (OR 1.29, 95% CI 1.11-1.50).
Family history of gastric cancer is strongly associated with specific subtypes of gastric cancer as well as with gastric atrophy, a risk factor for developing this malignancy.
家族史可能提示胃癌和癌前病变的风险。
我们在芬兰的一项前瞻性研究中,对 20720 名男性吸烟者中的 307 例新发胃癌病例进行了一级亲属癌症史的相关性研究。采用 Cox 回归计算胃癌风险比(HR)和 95%置信区间(95%CI)。采用 logistic 回归估计低血清胃蛋白酶原(胃萎缩的标志物)的比值比(OR)和 95%CI。
总体而言,胃癌风险与一级亲属的胃癌史(HR 1.56,95%CI 1.15-2.12)、父亲(HR 1.67,95%CI 1.09-2.55)和兄弟姐妹(HR 2.05,95%CI 1.25-3.38)相关。非贲门(HR 1.83,95%CI 1.30-2.57)但贲门(HR 0.93,95%CI 0.46-1.87)癌、肠型(HR 1.53,95%CI 0.92-2.55)和弥漫型(HR 1.47,95%CI 0.72-3.03)组织学亚型的相关性具有统计学意义。其他癌症类型的家族史与胃癌风险无关。胃癌家族史与低胃蛋白酶原(OR 1.29,95%CI 1.11-1.50)相关。
胃癌家族史与特定的胃癌亚型以及胃癌发生的危险因素胃萎缩密切相关。