Department of Clinical Medicine, Center for Molecular Prediction of Inflammatory Bowel Disease (PREDICT), Aalborg University, Copenhagen, Denmark.
Department of Epidemiology Research, Statens Serum Institut, Copenhagen, Denmark.
Int J Cancer. 2022 Oct 15;151(8):1261-1269. doi: 10.1002/ijc.34148. Epub 2022 Jun 22.
Risk of colorectal cancer (CRC) increases in relatives of patients with CRC. The extent to which this is attributable to genetic predisposition or shared environment is unclear. We explored this question using nationwide cohorts from Denmark, Finland and Sweden. From 1977 to 2013, we identified 359 879 individuals with a CRC diagnosis and 2 258 870 of their relatives who we followed for CRC incidence. We calculated standardized incidence ratios (SIR) and 95% confidence intervals (CI) for CRC in individuals with an affected relative. We used nationwide household and pedigree data along with national SIR estimates to calculate risk ratios (RR) for the contribution of shared household environment, childhood environment and genetic relationship to CRC risk in those with an affected relative. SIR of CRC was increased for individuals with an affected relative, across all countries and ages. For those with an affected parent, the SIR was 1.65 (95% CI: 1.61-1.69), 1.98 (95% CI: 1.87-2.09), for those with an affected sibling and 2.14 (95% CI: 1.84-2.49) for those with an affected halfsibling. In those <65 years old, shared childhood (RR: 1.41, 95% CI: 1.26-1.57) and household (RR: 2.08, 95% CI: 1.25-3.46) environments were significantly greater contributors to familial risk of CRC than genetics (RR: 0.88, 95% CI: 0.53-1.46). This large-scale Nordic population-based study of excess risk of CRC among relatives of those with CRC addresses the difficult disentangling of shared environment from genetic predisposition in the heritability of CRC. We found shared environment to be the most important contributor to CRC risk.
结直肠癌(CRC)患者的亲属 CRC 风险增加。但这种风险多大程度上归因于遗传易感性或共同环境尚不清楚。我们使用来自丹麦、芬兰和瑞典的全国性队列对此问题进行了探讨。1977 年至 2013 年间,我们确定了 359879 例 CRC 确诊患者及其 2258870 名亲属,并对他们进行 CRC 发病率随访。我们计算了有受影响亲属的个体 CRC 的标准化发病比(SIR)和 95%置信区间(CI)。我们使用全国性家庭和谱系数据以及全国 SIR 估计值来计算有受影响亲属的个体中共享家庭环境、儿童时期环境和遗传关系对 CRC 风险的贡献的风险比(RR)。在所有国家和年龄段,有受影响亲属的个体 CRC 的 SIR 均增加。对于有受影响的父母的个体,SIR 为 1.65(95%CI:1.61-1.69)、1.98(95%CI:1.87-2.09),对于有受影响的兄弟姐妹的个体为 2.14(95%CI:1.84-2.49),对于有受影响的同父异母或同母异父兄弟姐妹的个体为 2.14(95%CI:1.84-2.49)。对于<65 岁的个体,共享的儿童时期(RR:1.41,95%CI:1.26-1.57)和家庭(RR:2.08,95%CI:1.25-3.46)环境对 CRC 家族风险的贡献明显大于遗传(RR:0.88,95%CI:0.53-1.46)。这项针对 CRC 患者亲属 CRC 风险增加的大型北欧基于人群的研究解决了在 CRC 的遗传性中从遗传易感性中区分共享环境的难题。我们发现共享环境是 CRC 风险的最重要贡献因素。