Newcomb P A, Taylor J O, Trentham-Dietz A
Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
Int J Epidemiol. 1999 Aug;28(4):603-8. doi: 10.1093/ije/28.4.603.
Family history of colorectal cancer has been consistently associated with an increased personal risk of this disease. Since evidence suggests that hormones are related to colon cancer risk in women, the effect of family history on large bowel incidence may be modified according to endogenous and exogenous hormone levels.
We analysed data from a population-based case-control study of female colorectal cancer to evaluate family history and cancer risk. Cases (n = 702) were female residents of Wisconsin with a new diagnosis of colorectal cancer, identified through a statewide tumour registry. Controls (n = 2274) were randomly selected from lists of licensed drivers and from rosters of Medicare beneficiaries. All relative risks (RR) were adjusted for age, body mass index, smoking and alcohol history, education, and use of hormone replacement therapy.
Compared with women who reported no history of cancer in a first degree relative, women with a family history had an RR of 2.07 (95% confidence interval [CI]: 1.60-2.68). Regardless of which parent was affected, risks were increased about twofold, while sibling history was associated with about a 50% increase in risk. Risk was greater if more than one family member was affected (RR 3.65, 95% CI: 1.81-7.37). The association between family history and risk was stronger for colon cancer than for rectal cancer. There were no indications that exogenous hormonal factors, notably hormone replacement use, modified these risks. There was a suggestion that high parity attenuated the risks associated with family history (P = 0.07).
These results confirm that family history of colorectal cancer is associated with a doubling of risk for large bowel cancer in women; some histories were associated with greater risk. This relation was not substantially different among subgroups of women with varying exogenous and endogenous hormone exposures.
结直肠癌家族史一直与个人患此病的风险增加相关。由于有证据表明激素与女性结肠癌风险有关,家族史对大肠发病率的影响可能会根据内源性和外源性激素水平而改变。
我们分析了一项基于人群的女性结直肠癌病例对照研究的数据,以评估家族史与癌症风险。病例(n = 702)为威斯康星州新诊断为结直肠癌的女性居民,通过全州肿瘤登记处确定。对照(n = 2274)从持牌司机名单和医疗保险受益人名单中随机选取。所有相对风险(RR)均根据年龄、体重指数、吸烟和饮酒史、教育程度以及激素替代疗法的使用情况进行了调整。
与报告一级亲属无癌症病史的女性相比,有家族史的女性RR为2.07(95%置信区间[CI]:1.60 - 2.68)。无论哪位父母患病,风险都会增加约两倍,而兄弟姐妹有病史则与风险增加约50%相关。如果不止一名家庭成员患病,风险会更高(RR 3.65,95% CI:1.81 - 7.37)。家族史与结肠癌风险的关联比直肠癌更强。没有迹象表明外源性激素因素,特别是激素替代疗法的使用,会改变这些风险。有迹象表明高生育次数会降低与家族史相关的风险(P = 0.07)。
这些结果证实,结直肠癌家族史与女性患大肠癌的风险加倍有关;某些家族史与更高的风险相关。在不同外源性和内源性激素暴露的女性亚组中,这种关系没有实质性差异。