饮酒不会改变绝经后妇女乳腺癌多基因风险评分的遗传风险:社区动脉粥样硬化风险研究

Minghui Zhang, Meng Ru, Jingning Zhang, Ziqiao Wang, Jiayun Lu, Kenneth R Butler, Nilanjan Chatterjee, David J Couper, Anna E Prizment, Mehrnoosh M Soori, Kala Visvanathan, Cynthia A Zahnow, Corinne E Joshu, Elizabeth A Platz
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引用次数: 0

摘要

高遗传风险和饮酒量≥1杯/天与乳腺癌风险增加有关。然而,人们对酒精和遗传之间对乳腺癌风险的相互作用还知之甚少,包括在不富含每日饮酒者的人群中。我们对社区动脉粥样硬化风险研究中的 5651 名白人和黑人绝经后妇女进行了前瞻性研究。酒精摄入量通过食物频率问卷进行评估。计算了 313-SNPs 多基因风险评分(PRS)。乳腺癌病例主要通过截至 2015 年的癌症登记链接确定。采用多变量 Cox 回归估算 PRS 和当前乙醇摄入量与乳腺癌的相关性及其交互作用的危险比 (HR) 和 95% 置信区间 (CI)。50.6%的人目前饮酒,其中50.8%的人每周饮酒7次。在白人妇女(HR1-SD:1.48,95%CI:1.34-1.65)和黑人妇女(HR1-SD:1.15,95%CI:0.96-1.38)中,较高的PRS与较高的乳腺癌风险相关。目前的乙醇摄入量与乳腺癌风险之间未发现正相关(白人,HR13g/周:1.00,95%CI:0.98-1.03;黑人,HR:0.83,95%CI:0.69-1.00)。在白人和黑人女性中,PRS 似乎与饮酒者和不饮酒者的风险呈正相关。在白人和黑人女性中,没有证据表明PRS与乙醇摄入量之间存在相互作用。使用在非洲裔女性中开发的 89-SNP PRS 时,黑人女性的模式与之相似。总之,在一项针对白人和黑人绝经后妇女的前瞻性分析中,我们的研究结果表明,饮酒不会改变基于 PRS 的乳腺癌遗传风险。
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Alcohol Consumption Does not Modify the Polygenic Risk Score-Based Genetic Risk of Breast Cancer in Postmenopausal Women: Atherosclerosis Risk in Communities Study.

High genetic risk and alcohol consumption ≥1 drink/day are associated with increased breast cancer risk. However, the interaction between alcohol and genetics on breast cancer risk is poorly understood, including in populations not enriched with daily drinkers. We prospectively studied 5,651 White and Black postmenopausal women in the Atherosclerosis Risk in Communities study. Alcohol intake was assessed by a food frequency questionnaire. The 313-SNP polygenic risk score (PRS) was calculated. Breast cancer cases were ascertained primarily by cancer registry linkage through 2015. Multivariable Cox regression was used to estimate HRs and 95% confidence intervals (CI) for the association of PRS and current ethanol intake with breast cancer, and their interaction. Of these individuals, 50.6% were current drinkers, and of them, 50.8% drank <1 drink/week and 12.8% drank >7 drinks/week. A higher PRS was associated with a higher breast cancer risk among White (HR1-SD, 1.48; 95% CI, 1.34-1.65) and Black (HR1-SD, 1.15; 95% CI, 0.96-1.38) women. Positive associations were not observed between current ethanol intake and breast cancer risk (White: HR13 g/week, 1.00; 95% CI, 0.98-1.03; Black: HR, 0.83; 95% CI, 0.69-1.00). Among both White and Black women, PRS generally seemed to be positively associated with risk in drinkers and nondrinkers. There was no evidence of a PRS-ethanol intake interaction among White or Black women. Patterns in Black women were similar when using an 89-SNP PRS developed among African ancestry women. In conclusion, in a prospective analysis of White and Black postmenopausal women in a study population not enriched with daily drinkers, our findings suggest that alcohol drinking does not modify the PRS-based genetic risk of breast cancer. Prevention Relevance: Although our findings suggest that alcohol drinking does not modify the PRS-based genetic risk of breast cancer among White and Black women with lower alcohol intake, nevertheless, women should consider limiting alcohol consumption as a general cancer prevention strategy, as indicated in dietary guidelines.

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