Cardiovascular health, polygenic risk score, and cancer risk: a prospective cohort study

被引:0
|
作者
Peng, Yu [1 ]
Wang, Peng [1 ]
Du, Han [1 ]
Liu, Fubin [1 ]
Wang, Xixuan [1 ]
Si, Changyu [1 ]
Gong, Jianxiao [1 ]
Zhou, Huijun [1 ]
Chen, Kexin [1 ]
Song, Fangfang [1 ]
机构
[1] Tianjin Med Univ, Tianjin Med Univ Canc Inst & Hosp, Natl Clin Res Ctr Canc, Minist Educ,Key Lab Prevent & Control Major Dis Po, Tianjin, Peoples R China
来源
AMERICAN JOURNAL OF CLINICAL NUTRITION | 2024年 / 120卷 / 04期
基金
国家重点研发计划;
关键词
cardiovascular health; Life; Essential; 8; genetic predisposition; cancer; UK Biobank; LIFES ESSENTIAL 8; AMERICAN HEART ASSOCIATIONS; PROSTATE-CANCER; DISEASE; METAANALYSIS; MORTALITY;
D O I
10.1016/j.ajcnut.2024.07.033
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Background: Cancer and cardiovascular disease share common lifestyle risk factors. However, it remains unclear whether cardiovascular health (CVH) evaluated by Life's ' s Essential 8 can predict cancer risk, and attenuate the influence fl uence of genetic susceptibility on cancer. Objectives: We aimed to evaluate independent and joint associations of CVH and polygenic risk score (PRS) with risks of overall and site-specific fi c cancers. Methods: We undertook a population-based cohort study based on the UK Biobank. The CVH score was constructed by physical activity, body mass index, nicotine exposure, sleep, diet, blood pressure, lipid profile, fi le, and blood glucose. PRSs were assessed individually for 18 cancer types by their independent single-nucleotide polymorphisms previously identified fi ed in genome-wide association studies. Multivariable Cox proportional-hazards models were applied to explore the independent and joint associations of CVH and PRS with cancer incidence risk. The results were displayed as hazard ratio (HR) and 95% confidence fi dence interval (CI). Results: Compared with low CVH, high CVH was associated with decreased risks of overall cancer and the majority of common cancers, including digestive system [HRs (95% CI): 0.33 (0.23, 0.45)-0.66 - 0.66 (0.58, 0.75)], lung (HR: 0.25; 95% CI: 0.21, 0.31), renal (HR: 0.42; 95% CI: 0.32, 0.56), bladder (HR: 0.55; 95% CI: 0.44, 0.69), breast (HR: 0.83; 95% CI: 0.74, 0.92), and endometrial cancers (HR: 0.39; 95% CI: 0.30, 0.51). For overall cancer in males, there was an interaction between CVH and PRS. Notably, individuals with high CVH across all levels of PRS had lower risks of overall cancer for females and 8 site-specific fi c cancers than those with low CVH and high PRS [HRs (95% CIs): 0.18 (0.12, 0.25)-0.79 - 0.79 (0.71, 0.87)]. Conclusions: High CVH was related to decreased risks of overall cancer and multiple cancers regardless of genetic predispositions. Our fi ndings underscored the value of improving CVH for cancer prevention in the general population.
引用
收藏
页码:785 / 793
页数:9
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