Associations of combined lifestyle and metabolic risks with cancer incidence in the UK biobank study.

IF 3.4 2区 医学 Q2 ONCOLOGY
Feng Lin, Wen Hu, Chenfenglin Yang, Binglin Cheng, Hongfan Chen, Jiaxin Li, Hanrui Zhu, Haixiang Zhang, Xiang Yuan, Xianyue Ren, Xiaohong Hong, Xinran Tang
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引用次数: 0

Abstract

Background: Although metabolic syndrome (MetS) is associated with an increased risk of various cancers, the combined impact of MetS and healthy lifestyle factors (HLF) on cancer risk is unclear. This study aimed to investigate the independent and combined effects of MetS and HLF on the risk of 16 site-specific cancers in a large community-based cohort.

Methods: A total of 289,557 participants in the UK Biobank were analyzed. MetS was defined using a combination of metabolic factors, while HLF scores were evaluated based on lifestyle behaviors, such as smoking, alcohol consumption, physical activity, and diet. Cox proportional hazard models were used to investigate the relationship between MetS or HLF and cancer risk, adjusting for age, sex, ethnicity, education level, family history of cancer, and the Townsend Deprivation Index (TDI).

Results: During a median follow-up of 11.69 years, 11,190 individuals developed cancer. MetS was associated with an increased risk of 9 cancers in men and 7 cancers in women. Compared with participants with unfavorable lifestyles, regardless of metabolic status, HLF was significantly associated with decreased risk of overall cancer (without MetS: HR: 0.812; 95% CI: 0.745-0.886 for intermediate lifestyle and HR: 0.757; 95% CI: 0.669-0.855 for favorable lifestyle; with MetS: HR: 0.702; 95% CI: 0.572-0.862 for favorable lifestyle) and oesophagus, stomach, liver, lung, bronchus, trachea cancers in men and of lung, bronchus, trachea cancers in women. Our analysis demonstrated that the protective association between HLF and reduced cancer risk was confined to subgroups without MetS. Specifically, this association was observed for cancers of the lip, oral cavity, pharynx, colon, rectum, pancreas, kidney, bladder, and lymphoid leukemia in men, and for overall cancer in women(HR: 0.917; 95% CI: 0.862-0.975 for intermediate lifestyle and HR: 0.875; 95% CI: 0.817-0.938 for favorable lifestyle).

Conclusion: MetS elevates risks for multiple cancers, while adopting a healthy lifestyle reduces risks of oesophagus, stomach, and lung, bronchus, trachea cancers in men and lung, bronchus, trachea cancer in women, regardless of metabolic status. However, MetS counteracts lifestyle-mediated protection against specific cancers-including lip, oral cavity, pharynx, colon, rectum, pancreas, kidney, and bladder cancers in men, as well as pancreas and breast cancers in women. These findings underscore the necessity to develop metabolic status-stratified management strategies and implement proactive prevention of MetS.

英国生物银行研究中生活方式和代谢风险与癌症发病率的关系
背景:虽然代谢综合征(MetS)与各种癌症的风险增加有关,但MetS和健康生活方式因素(HLF)对癌症风险的综合影响尚不清楚。本研究旨在调查MetS和HLF对大型社区队列中16种部位特异性癌症风险的独立和联合影响。方法:对英国生物银行289,557名参与者进行分析。MetS是通过代谢因素的组合来定义的,而HLF评分是根据生活方式行为来评估的,如吸烟、饮酒、体育活动和饮食。在调整年龄、性别、种族、教育水平、癌症家族史和汤森剥夺指数(TDI)等因素后,采用Cox比例风险模型调查met或HLF与癌症风险之间的关系。结果:在中位随访11.69年期间,11,190人患上了癌症。MetS与男性患9种癌症和女性患7种癌症的风险增加有关。与生活方式不良的参与者相比,无论代谢状态如何,HLF与总体癌症风险降低显著相关(无MetS: HR: 0.812;中等生活方式的95% CI: 0.745-0.886, HR: 0.757;良好生活方式的95% CI: 0.669-0.855;met: HR: 0.702;95% CI: 0.572-0.862(良好的生活方式)男性的食道,胃,肝,肺,支气管,气管癌女性的肺,支气管,气管癌。我们的分析表明,HLF与降低癌症风险之间的保护性关联仅限于没有MetS的亚组。具体来说,男性的唇癌、口腔癌、咽喉癌、结肠癌、直肠癌、胰腺癌、肾癌、膀胱癌和淋巴性白血病以及女性的总体癌症都存在这种关联(HR: 0.917;中等生活方式组95% CI: 0.862-0.975, HR: 0.875;良好生活方式的95% CI: 0.817-0.938)。结论:无论代谢状态如何,met可增加多种癌症的风险,而健康的生活方式可降低男性食道、胃、肺、支气管、气管癌和女性肺、支气管、气管癌的风险。然而,met抵消了生活方式对特定癌症的保护作用,包括男性的唇部、口腔、咽部、结肠、直肠、胰腺、肾脏和膀胱癌,以及女性的胰腺和乳腺癌。这些发现强调了制定代谢状态分层管理策略和实施主动预防MetS的必要性。
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
BMC Cancer
BMC Cancer 医学-肿瘤学
CiteScore
6.00
自引率
2.60%
发文量
1204
审稿时长
6.8 months
期刊介绍: BMC Cancer is an open access, peer-reviewed journal that considers articles on all aspects of cancer research, including the pathophysiology, prevention, diagnosis and treatment of cancers. The journal welcomes submissions concerning molecular and cellular biology, genetics, epidemiology, and clinical trials.
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