Zhang Yin, Lindström Sara, Kraft Peter, Liu Yuxi
Department of Nutrition, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Department of Epidemiology, University of Washington, Seattle, WA, USA.
J Natl Cancer Inst. 2025 Jan 1;117(1):40-48. doi: 10.1093/jnci/djae208.
Early-onset cancer (diagnosed under age 50) generally manifests as an aggressive disease phenotype. The association between healthy lifestyle and early-onset cancer and whether it varies by common genetic variants remains unclear.
We analyzed a prospective cohort of 66 308 participants who were under age 50 and free of cancer at baseline in the UK Biobank. Using Cox regression, we estimated hazard ratios (HRs) and 95% confidence intervals (CIs) for early-onset total and breast cancer based on sex-specific composite total cancer polygenic risk scores (PRSs), a breast cancer-specific PRS, and sex-specific health-associated lifestyle scores (HLSs).
In multivariable-adjusted analyses with 2-year latency, higher genetic risk (highest vs lowest tertile of PRS) was associated with significantly increased risks of early-onset total cancer in females (HR, 95% CI = 1.83, 1.49 to 2.26) and males (2.03, 1.51 to 2.73) as well as early-onset breast cancer in females (3.06, 2.20 to 4.26). An unfavorable lifestyle (highest vs lowest category of HLS) was associated with higher risk of total cancer and breast cancer in females across genetic risk categories; the association with total cancer and breast cancer was stronger in the highest genetic risk category than the lowest: HRs (95% CIs) were 1.55 (1.12 to 2.14) and 1.69 (1.11 to 2.57) in the highest genetic risk category and 1.03 (0.64 to 1.67) and 0.81 (0.36 to 1.85) in the lowest.
Genetic and lifestyle factors were independently associated with early-onset total and breast cancer risk. Individuals with a high genetic risk may benefit more from adopting a healthy lifestyle in preventing early-onset cancer.
早发性癌症(50岁之前确诊)通常表现为侵袭性疾病表型。健康生活方式与早发性癌症之间的关联以及这种关联是否因常见基因变异而有所不同仍不清楚。
我们分析了英国生物银行中66308名50岁以下且基线时无癌症的参与者的前瞻性队列。使用Cox回归,我们基于性别特异性综合总癌症多基因风险评分(PRS)、乳腺癌特异性PRS以及性别特异性健康相关生活方式评分(HLS),估计早发性总癌症和乳腺癌的风险比(HR)及95%置信区间(CI)。
在有2年潜伏期的多变量调整分析中,较高的遗传风险(PRS最高三分位数与最低三分位数相比)与女性(HR,95%CI = 1.83,1.49至2.26)和男性(2.03,1.51至2.73)早发性总癌症以及女性早发性乳腺癌(3.06,2.20至4.26)的风险显著增加相关。不良生活方式(HLS最高类别与最低类别相比)与各遗传风险类别中女性的总癌症和乳腺癌风险较高相关;在最高遗传风险类别中与总癌症和乳腺癌的关联比最低类别更强:最高遗传风险类别中的HR(95%CI)分别为1.55(1.12至2.14)和1.69(1.11至2.57),最低类别中分别为1.03(0.64至1.67)和0.81(0.36至1.85)。
遗传和生活方式因素与早发性总癌症和乳腺癌风险独立相关。遗传风险高的个体在预防早发性癌症方面可能从采用健康生活方式中获益更多。