Imsland Albert Kjartansson, Eldon Bjarki Jónsson, Arinbjarnarson Sturla, Egilsson Valgarğur, Tulinius Hrafn, Tryggvadóttir Laufey, Arngrímsson Reynir, Magnússon Jónas
Iceland Genomics Corporation, Reykjavik.
J Am Coll Surg. 2002 Aug;195(2):181-6; discussion 186-7. doi: 10.1016/s1072-7515(02)01215-2.
Association between gastric cancer and environmental factors (diet and infections) has been established, and genetic changes are well described in adenocarcinomas of the stomach. Less is known about clinical features of hereditary gastric cancer and whether the disease is associated with family clustering.
Family trees of patients diagnosed with gastric cancer in Iceland between 1955 and 1999 were identified in the Genealogical Database of the University of Iceland. All probands with age of onset younger than 60 years were used in the study. Families of all probands (n = 455 men and 161 women) were traced to third degree. Through linkage of the genealogic data obtained by the Icelandic Cancer Registry (between 1955 and 1999), all reported cancers were identified in those families. The expected number of cases was calculated using age-specific population rates in Iceland.
A relative risk (RR) of 2.2 (95% confidence interval [CI] = 1.6-3.0) and 1.3 (95% CI = 1.0-1.7) for the gastric cancer risk was observed among 2,846 first- and 8,658 second-degree relatives of male probands. For female probands the corresponding relative risks were 1.6 (95% CI = 1.1-2.6, n = 7,396) and 1.4 (95% CI = 0.9-2.0, n = 2,764). The increased risk was more pronounced for relatives of men and women diagnosed with gastric cancer before the age of 50 years. A minor difference in relative risk was found between relatives of probands who were diagnosed with intestinal type or diffuse type gastric cancer. Fifty-eight families with two or more relatives with cancer were identified. In 32 families 2 relatives with gastric cancer were identified and in 26 families 3 or more relatives had gastric cancer.
Relatives of gastric cancer patients have two- to three-fold increased risk of developing gastric cancer. The risk is elevated for both genders.
胃癌与环境因素(饮食和感染)之间的关联已得到证实,胃癌腺癌中的基因变化也有详细描述。关于遗传性胃癌的临床特征以及该疾病是否与家族聚集性相关,人们了解得较少。
在冰岛大学的家谱数据库中识别出1955年至1999年间在冰岛被诊断为胃癌的患者的家族树。研究中使用了所有发病年龄小于60岁的先证者。所有先证者(455名男性和161名女性)的家族追溯到第三代。通过冰岛癌症登记处(1955年至1999年)获得的家谱数据的关联,在这些家族中识别出所有报告的癌症。使用冰岛的年龄特异性人口发病率计算预期病例数。
在男性先证者的2846名一级亲属和8658名二级亲属中,观察到患胃癌风险的相对风险(RR)分别为2.2(95%置信区间[CI]=1.6 - 3.0)和1.3(95% CI = 1.0 - 1.7)。对于女性先证者,相应的相对风险分别为1.6(95% CI = 1.1 - 2.6,n = 7396)和1.4(95% CI = 0.9 - 2.0,n = 2764)。对于被诊断为胃癌且发病年龄在50岁之前的男性和女性的亲属,风险增加更为明显。在被诊断为肠型或弥漫型胃癌的先证者的亲属之间,相对风险存在微小差异。识别出58个有两名或更多亲属患癌症的家族。在32个家族中识别出两名患胃癌的亲属,在26个家族中三名或更多亲属患胃癌。
胃癌患者的亲属患胃癌的风险增加两到三倍。男女风险均升高。