侵袭性前列腺癌的风险与连续几代美国拉丁裔男性

Fei Chen, Adelynn Paik, Xin Sheng, Iona Cheng, Salma Shariff-Marco, Lynne R Wilkens, Loïc Le Marchand, David V Conti, Christopher A Haiman, Veronica Wendy Setiawan
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引用次数: 0

摘要

背景:美国出生的拉丁裔男性前列腺癌(PCa)的发病率高于外国出生的拉丁裔男性。目前尚不清楚这些增加是否完全是由于美国PCa检出率的增加,PCa危险因素的变化,或两者的结合。方法在多种族队列(MEC)中,我们评估了19597名拉丁裔男性的代际地位与PCa风险之间的关系,调整了人口统计学和生活方式因素、个人和社区社会经济地位(SES)以及PSA筛查史。在具有遗传数据的生物库队列中,敏感性分析包括对多基因风险评分(PRS)和遗传祖先的额外调整。结果该分析包括10,241第一代,4,610第二代和4,746第三代拉丁裔男性,其中2,366人在平均19.2年的随访期间被诊断为PCa。在调整协变量后,我们观察到代际状态与整体、局部或低级别PCa风险之间没有关联。每一代的增加与高级别、晚期或侵袭性PCa的风险增加13%至15%显著相关。这些与侵袭性前列腺癌的关联在生物库队列中仍然显著,并对PRS和遗传血统进行了额外的调整。结论:在美国,拉美裔男性患侵袭性前列腺癌的风险增加与世代相关,而观察到的增加不能用遗传易感性、血统、PSA筛查、生活方式和SES因素的差异来解释。需要进一步调查以确定导致这种风险增加的其他因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Risk of aggressive prostate cancer with successive generations in the U.S. among Latino men
Background US-born Latino men have a higher incidence of prostate cancer (PCa) than foreign-born Latino men. It was not clear whether these increases were exclusively due to increased detection of PCa in the US, changes in risk factors of PCa, or a combination of both. Methods In the Multiethnic Cohort (MEC) we evaluated the association between generational status and risk of PCa in 19,597 Latino men, adjusting for demographic and lifestyle factors, individual- and neighborhood-level socioeconomic status (SES), as well as history of PSA screening. Additional adjustments on polygenic risk score (PRS) and genetic ancestry were included in the sensitivity analysis in the biorepository cohort with genetic data. Results This analysis included 10,241 1st-generation, 4,610 2nd-generation, and 4,746 3rd-generation Latino men, among whom 2,366 PCa were diagnosed during an average of 19.2 years of follow-up. After adjusting for covariates, we observed no association between generational status and risk of overall, localized, or low-grade PCa. A per generation increase was significantly associated with a 13% to 15% elevated risk of high-grade, advanced, or aggressive PCa. These associations with aggressive forms of PCa remained significant in the biorepository cohort with additional adjustment on PRS and genetic ancestry. Conclusions Successive generations in the US were associated with an increased risk of aggressive forms of PCa among Latino men and the observed increases cannot be explained by differences in genetic susceptibility, ancestry, PSA screening, lifestyle, and SES factors. Further investigations are needed to identify additional factors that contribute to this increased risk.
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