Genetic Risk, Health-Associated Lifestyle, and Risk of Early-onset Total Cancer and Breast Cancer.

IF 9.9 1区 医学 Q1 ONCOLOGY
Yin Zhang, Sara Lindström, Peter Kraft, Yuxi Liu
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引用次数: 0

Abstract

Background: 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.

Methods: 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).

Results: 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, 1.49-2.26) and males (2.03, 1.51-2.73) as well as early-onset breast cancer in females (3.06, 2.20-4.26). 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, 2.14) and 1.69 (1.11, 2.57) in the highest genetic risk category and 1.03 (0.64, 1.67) and 0.81 (0.36, 1.85) in the lowest.

Conclusions: 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.

遗传风险、与健康相关的生活方式以及早发全癌和乳腺癌的风险。
背景:早发癌症(50 岁以下确诊)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系,以及这种关系是否因常见基因变异而有所不同,目前仍不清楚:我们对英国生物库中 66,308 名年龄在 50 岁以下且基线时未患癌症的参与者进行了前瞻性队列分析。我们根据性别特异性总癌症多基因风险综合评分(PRS)、乳腺癌特异性多基因风险评分和性别特异性健康相关生活方式评分(HLS),使用 Cox 回归估算了早发总癌症和乳腺癌的危险比(HRs)和 95% 置信区间(CIs):在对 2 年潜伏期进行的多变量调整分析中,女性(HR,95% CI:1.83,1.49-2.26)和男性(2.03,1.51-2.73)患早发总癌以及女性(3.06,2.20-4.26)患早发乳腺癌的风险与较高的遗传风险(PRS 最高与最低三等分)显著相关。在不同的遗传风险类别中,不利的生活方式(HLS最高类别与最低类别)与女性罹患总癌症和乳腺癌的风险较高相关;遗传风险最高类别与总癌症和乳腺癌的相关性比最低类别更强:最高遗传风险类别的 HRs(95% CIs)分别为 1.55(1.12,2.14)和 1.69(1.11,2.57),最低遗传风险类别的 HRs(95% CIs)分别为 1.03(0.64,1.67)和 0.81(0.36,1.85):遗传和生活方式因素与早发性总乳腺癌和乳腺癌风险独立相关。结论:遗传和生活方式因素与早发总乳腺癌和乳腺癌的风险独立相关。遗传风险高的人可能更受益于采用健康的生活方式来预防早发癌症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
17.00
自引率
2.90%
发文量
203
审稿时长
4-8 weeks
期刊介绍: The Journal of the National Cancer Institute is a reputable publication that undergoes a peer-review process. It is available in both print (ISSN: 0027-8874) and online (ISSN: 1460-2105) formats, with 12 issues released annually. The journal's primary aim is to disseminate innovative and important discoveries in the field of cancer research, with specific emphasis on clinical, epidemiologic, behavioral, and health outcomes studies. Authors are encouraged to submit reviews, minireviews, and commentaries. The journal ensures that submitted manuscripts undergo a rigorous and expedited review to publish scientifically and medically significant findings in a timely manner.
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