Familial Risk and Interaction With Smoking and Alcohol Consumption in Bladder Cancer: A Population-Based Cohort Study

被引:0
|
作者
Kim, Hyun Jung [1 ]
Kim, Kyoung-Hoon [2 ]
Lee, Sung Won [3 ]
Swan, Heather [1 ]
Kazmi, Sayada Zartasha [4 ]
Kim, Young Shin [1 ]
Kim, Kyeong Uoon [5 ]
Kim, Minjung [6 ]
Cha, Jaewoo [6 ]
Kang, Taeuk [7 ]
Hann, Hoo Jae [8 ]
Ahn, Hyeong Sik [1 ,9 ]
机构
[1] Korea Univ, Coll Med, Dept Prevent Med, Seoul 02841, South Korea
[2] Hlth Insurance Review & Assessment Serv, Evidence Based Res Div, Wonju 26465, Gangwon Do, South Korea
[3] Sungkyunkwan Univ, Samsung Biomed Res Inst, Samsung Med Ctr, Sch Med,Dept Urol, Seoul 06351, South Korea
[4] Seoul Natl Univ, Dept Prevent Med, Coll Med, Seoul 03080, South Korea
[5] Seojeong Univ, Dept Nursing, Yangju, Gyeonggi Do, South Korea
[6] Korea Univ, Grad Sch, Dept Publ Hlth, Seoul, South Korea
[7] Sungshin Womens Univ, Hlth & Wellness Coll, Seoul, South Korea
[8] Ewha Womans Univ, Med Res Inst, Coll Med, Seoul, South Korea
[9] Korea Univ, Coll Med, Dept Prevent Med, Seoul 02841, South Korea
关键词
Bladder cancer; Familial risk; Additive interaction; Smoking; Alcohol consumption;
D O I
10.14740/wjon1639
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: 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.Methods: Using the National Health Insurance database, we con-structed 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).Results: 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). Conclusion: 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.
引用
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页码:382 / 391
页数:10
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