Flander Louisa, Speirs-Bridge Andrew, Rutstein Alison, Niven Heather, Win Aung Ko, Ait Ouakrim Driss, Hopper John L, Macrae Finlay, Keogh Louise, Gaff Clara, Jenkins Mark
Centre for Molecular, Environmental, Genetic & Analytic Epidemiology, The University of Melbourne, Melbourne, VIC, 3010, Australia,
J Genet Couns. 2014 Feb;23(1):79-88. doi: 10.1007/s10897-013-9614-2. Epub 2013 Jun 9.
People carrying germline mutations in mismatch repair genes are at high risk of colorectal cancer (CRC), yet about half of people from mutation-carrying families decline genetic counselling and/or testing to identify mutation status. We studied the association of quantitative measures of risk perception, risk prediction and self-reported screening colonoscopy in this elusive yet high-risk group. The sample of 26 participants (mean age 43.1 years, 14 women) in the Australasian Colorectal Cancer Family Registry were relatives of mutation carriers; had not been diagnosed with any cancer at the time of recruitment and had declined an invitation to attend genetic counselling and/or testing. A structured elicitation protocol captured perceived CRC risk over the next 10 years. Self-reported colonoscopy screening was elicited during a 45-minute semi-structured interview. Predicted 10-year CRC risk based on age, gender, known mutation status and family history was calculated using "MMRpro." Mean perceived 10-year risk of CRC was 31 % [95 % CI 21, 40], compared with mean predicted risk of 4 % [2, 7] (p < 0.001); this was independent of age and sex (p = 0.9). Among those reporting any medical advice and any screening colonoscopy (n = 18), those with higher risk perception had less frequent colonoscopy (Pearson's r = 0.49 [0.02, 0.79]). People who decline genetic testing for CRC susceptibility mutations perceive themselves to be at substantially higher risk than they really are. Those with high perceived risk do not undertake screening colonoscopy more often than those who perceive themselves to be at average risk.
携带错配修复基因种系突变的人患结直肠癌(CRC)的风险很高,但来自携带突变家庭的人中约有一半拒绝接受遗传咨询和/或检测以确定突变状态。我们研究了在这个难以捉摸但高危群体中,风险感知、风险预测的定量测量与自我报告的结肠镜筛查之间的关联。澳大利亚结直肠癌家族登记处的26名参与者(平均年龄43.1岁,14名女性)样本是突变携带者的亲属;在招募时未被诊断出患有任何癌症,并且拒绝了参加遗传咨询和/或检测的邀请。一个结构化的诱导方案记录了未来10年感知到的结直肠癌风险。在45分钟的半结构化访谈中引出自我报告的结肠镜筛查情况。使用“MMRpro”根据年龄、性别、已知突变状态和家族史计算预测的10年结直肠癌风险。感知到的10年结直肠癌平均风险为31%[95%CI 21,40],相比之下,平均预测风险为4%[2,7](p<0.001);这与年龄和性别无关(p = 0.9)。在报告接受过任何医疗建议和进行过任何结肠镜筛查的人中(n = 18),风险感知较高的人结肠镜检查频率较低(Pearson相关系数r = 0.49[0.02,0.79])。拒绝进行结直肠癌易感性突变基因检测的人认为自己的风险比实际风险高得多。风险感知高的人并不比认为自己风险平均的人更常进行结肠镜筛查。