Murff Harvey J, Peterson Neeraja B, Fowke Jay H, Hargreaves Margaret, Signorello Lisa B, Dittus Robert S, Zheng Wei, Blot William J
Vanderbilt Epidemiology Center, Nashville, TN 37203-1738, USA.
Arch Intern Med. 2008 Mar 24;168(6):625-31. doi: 10.1001/archinte.168.6.625.
Family history is a risk factor for colon cancer, and guidelines recommend initiating screening at age 40 years in individuals with affected relatives. Racial differences in colon cancer mortality could be related to variations in screening of increased-risk individuals.
Baseline data from 41 830 participants in the Southern Community Cohort Study were analyzed to determine the proportion of colonoscopy procedures in individuals with strong family histories of colon cancer, and whether differences existed based on race.
In participants with multiple affected first-degree relatives (FDRs) or relatives diagnosed before age 50 years, 27.3% (95% confidence interval [CI], 23.5%-31.1%) of African Americans reported having a colonoscopy within the past 5 years compared with 43.1% (95% CI, 37.0%-49.2%) of white participants (P<.001). African Americans in this group had an odds ratio of 0.51 (95% CI, 0.38-0.68) of having undergone recommended screening procedures compared with white participants after adjusting for age, sex, educational status, annual income, insurance status, total number of affected and unaffected FDRs, and time since last medical visit. African Americans with multiple affected FDRs or relatives diagnosed before age 50 years and who had ever undergone endoscopy were less likely to report a personal history of colon polyps (odds ratio, 0.29; 95% CI, 0.20-0.42) when compared with whites with similar family histories.
African Americans who have FDRs with colon cancer are less likely to undergo colonoscopy screening compared with whites who have affected relatives. Increased efforts need to be directed at identifying and managing underserved populations at increased risk for colon cancer based on their family histories.
家族史是结肠癌的一个风险因素,指南建议有患病亲属的个体在40岁时开始进行筛查。结肠癌死亡率的种族差异可能与高危个体筛查的差异有关。
分析了南方社区队列研究中41830名参与者的基线数据,以确定有结肠癌家族史的个体中结肠镜检查的比例,以及是否存在基于种族的差异。
在有多个患病一级亲属(FDR)或在50岁之前被诊断出患病亲属的参与者中,27.3%(95%置信区间[CI],23.5%-31.1%)的非裔美国人报告在过去5年内进行过结肠镜检查,而白人参与者的这一比例为43.1%(95%CI,37.0%-49.2%)(P<0.001)。在调整了年龄、性别、教育程度、年收入、保险状况、患病和未患病FDR的总数以及上次就诊后的时间后,该组非裔美国人接受推荐筛查程序的比值比为0.51(95%CI,0.38-0.68),与白人参与者相比。有多个患病FDR或在50岁之前被诊断出患病亲属且曾接受过内镜检查的非裔美国人,与有相似家族史的白人相比,报告有结肠息肉个人史的可能性较小(比值比,0.29;95%CI,0.20-0.42)。
与有患病亲属的白人相比,有患结肠癌FDR的非裔美国人接受结肠镜检查筛查的可能性较小。需要加大力度,根据家族史识别和管理结肠癌高危的服务不足人群。