Kim Hyun Jung, Kim Kyoung-Hoon, Lee Sung Won, Swan Heather, Kazmi Sayada Zartasha, Kim Young Shin, Kim Kyeong Uoon, Kim Minjung, Cha Jaewoo, Kang Taeuk, Hann Hoo Jae, Ahn Hyeong Sik
Department of Preventive Medicine, College of Medicine, Korea University, Seoul 02841, Korea.
Evidence-Based Research Division, Health Insurance Review and Assessment Service, Gangwon-do (Bangok-dong) 26465, Korea.
World J Oncol. 2023 Oct;14(5):382-391. doi: 10.14740/wjon1639. Epub 2023 Sep 20.
Although genetic factors are known to play a role in the pathogenesis of bladder cancer, population-level familial risk estimates are scarce. We aimed to quantify the familial risk of bladder cancer and analyze interactions between family history and smoking or alcohol consumption.
Using the National Health Insurance database, we constructed a cohort of 5,524,403 study subjects with first-degree relatives (FDRs) and their lifestyle risk factors from 2002 to 2019. Familial risk was calculated using hazard ratios (HRs) with 95% confidence intervals (CIs) that compare the risk of individuals with and without affected FDRs. Interactions between family history and smoking or alcohol intake were assessed on an additive scale using the relative excess risk due to interaction (RERI).
Offspring with an affected parent had a 2.09-fold (95% CI: 1.41 - 3.08) increased risk of disease compared to those with unaffected parents. Familial risks of those with affected father and mother were 2.26 (95% CI: 1.51 - 3.39) and 1.10 (95% CI: 0.27 - 4.41), respectively. When adjusted for lifestyle factors, HR reduced slightly to 2.04 (95% CI: 1.38 - 3.01), suggesting that a genetic predisposition is the main driver in the familial aggregation. Smokers with a positive family history had a markedly increased risk of disease (HR: 3.60, 95% CI: 2.27 - 5.71), which exceeded the sum of their individual risks, with statistically significant interaction (RERI: 0.72, 95% CI: 0.31 - 1.13). For alcohol consumption, drinkers with a positive family history also had an increased risk of disease, although the interaction was not statistically significant (RERI: 0.05, 95% CI: -3.39 - 3.48).
Smokers and alcohol consumers with a positive family history of bladder cancer should be considered a high-risk group and be advised to undergo genetic counseling.
虽然已知遗传因素在膀胱癌的发病机制中起作用,但人群层面的家族风险估计却很稀少。我们旨在量化膀胱癌的家族风险,并分析家族史与吸烟或饮酒之间的相互作用。
利用国民健康保险数据库,我们构建了一个由5524403名研究对象组成的队列,这些对象在2002年至2019年期间有一级亲属(FDRs)及其生活方式风险因素。使用风险比(HRs)及95%置信区间(CIs)计算家族风险,该风险比用于比较有和没有受影响的FDRs的个体的患病风险。使用因相互作用导致的相对超额风险(RERI),在相加尺度上评估家族史与吸烟或饮酒之间的相互作用。
与父母未患病的后代相比,父母患病的后代患膀胱癌的风险增加了2.09倍(95%CI:1.41 - 3.08)。父亲和母亲患病的后代的家族风险分别为2.26(95%CI:1.51 - 3.39)和1.10(95%CI:0.27 - 4.41)。在对生活方式因素进行调整后,HR略有下降至2.04(95%CI:1.38 - 3.01),这表明遗传易感性是家族聚集的主要驱动因素。有家族史的吸烟者患膀胱癌的风险显著增加(HR:3.60,95%CI:2.27 - 5.71),这超过了他们个体风险的总和,且存在统计学上显著的相互作用(RERI:0.72,95%CI:0.31 - 1.13)。对于饮酒,有家族史的饮酒者患膀胱癌的风险也增加了,尽管这种相互作用没有统计学意义(RERI:0.05,95%CI:-3.39 - 3.48)。
有膀胱癌家族史的吸烟者和饮酒者应被视为高危人群,并建议他们接受遗传咨询。