Gut microbiome mediates the associations between lifestyle factors and risk of colorectal high-risk adenoma: results from a population-based cohort study.

IF 4.6 2区 生物学 Q1 MICROBIOLOGY
mSystems Pub Date : 2025-09-22 DOI:10.1128/msystems.00933-25
Kai Song, Jiahui Luo, Yuhan Zhang, Dong Wu, Hongda Chen, Min Dai
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引用次数: 0

Abstract

Lifestyle factors exert influence on the risk of colorectal cancer (CRC) and its precursors. However, the interaction between gut microbiota and lifestyle factors concerning colorectal high-risk adenomas (HRAs), as well as the specific microbial taxa implicated, remains underexplored. Here, we aimed to investigate the impact of common lifestyle factors on HRAs and to explore the potential mediating roles of gut microbiota in these effects. A total of 3,827 participants were enrolled from our multicenter CRC screening cohort. Lifestyle factors over the 12 months preceding enrollment were assessed via questionnaires. Fecal samples were collected upon enrollment and analyzed using 16S rRNA sequencing. Multivariate analyses were used to identify lifestyle-related risk factors for HRA, followed by the application of the multivariate association with linear models (MaAsLin2) to explore associations between microbiota and lifestyle risk factors, with causal mediation analysis employed to evaluate the gut microbiota's mediating effect between lifestyle factors and HRA risk. A total of 272 patients with HRA and 1,253 controls were included. Independent risk factors for HRA were identified as high body mass index, number of pack-years smoked >30, alcohol consumption >4 units/week. These lifestyle factors were significantly associated with the relative abundance of various microbial genera. Notably, genus Fusobacterium and Tyzzerella 4 were found to partially mediate the increased risk of HRA due to alcohol and cigarette consumption, respectively. These findings provide new insights for microbiota-targeted interventions or lifestyle-based prevention strategies to reduce the risk of CRC, offering a novel and actionable approach to early prevention.IMPORTANCELifestyle choices, such as diet, smoking, and alcohol consumption, are known to influence colorectal cancer risk, but the role of gut bacteria in mediating this process remains underestimated. To address this gap, our study aimed to explore the connections between lifestyle factors, gut microbes, and colorectal precancerous growths, referred to as high-risk adenomas (HRAs). We observed a dual association whereby obesity, heavy smoking, and excessive alcohol consumption were linked to both an increased risk of HRAs and distinct changes in gut bacteria. Importantly, smoking and alcohol consumption are associated with increased cancer risk, in part, through certain bacteria such as genus Fusobacterium and Tyzzerella 4. These findings reveal how gut microbes may act as a hidden bridge between lifestyle and disease development. Our discovery of these microbial mediators reveals novel opportunities for HRA prevention through lifestyle modifications or probiotic interventions targeting this carcinogenic pathway prior to malignant transformation.CLINICAL TRIALSThis study is registered with the Chinese Clinical Trial Registry as ChiCTR1800015506.

肠道微生物组介导生活方式因素与结直肠高危腺瘤风险之间的关联:一项基于人群的队列研究结果
生活方式因素对结直肠癌(CRC)及其前体的风险有影响。然而,肠道微生物群与结直肠高危腺瘤(HRAs)相关的生活方式因素之间的相互作用,以及所涉及的特定微生物分类群,仍未得到充分探讨。在这里,我们的目的是研究常见生活方式因素对HRAs的影响,并探讨肠道微生物群在这些影响中的潜在介导作用。我们的多中心CRC筛查队列共纳入3827名参与者。通过问卷调查评估入组前12个月的生活方式因素。入组时收集粪便样本,采用16S rRNA测序进行分析。采用多因素分析确定生活方式相关的HRA危险因素,应用多因素关联线性模型(MaAsLin2)探讨微生物群与生活方式危险因素之间的关系,采用因果中介分析评估肠道微生物群在生活方式因素与HRA风险之间的中介作用。共纳入272例HRA患者和1253例对照。HRA的独立危险因素被确定为高身体质量指数、吸烟包年数100 - 30、饮酒量100 - 4单位/周。这些生活方式因素与各种微生物属的相对丰度显著相关。值得注意的是,梭杆菌属和Tyzzerella 4分别在一定程度上介导了酒精和香烟消费导致的HRA风险增加。这些发现为针对微生物群的干预或基于生活方式的预防策略提供了新的见解,以降低结直肠癌的风险,为早期预防提供了一种新颖可行的方法。生活方式的选择,如饮食、吸烟和饮酒,已知会影响结直肠癌的风险,但肠道细菌在介导这一过程中的作用仍被低估。为了解决这一差距,我们的研究旨在探索生活方式因素、肠道微生物和结直肠癌前生长(即高风险腺瘤)之间的联系。我们观察到一种双重关联,即肥胖、大量吸烟和过度饮酒与HRAs风险增加和肠道细菌的明显变化有关。重要的是,吸烟和饮酒与癌症风险增加有关,这在一定程度上是通过某些细菌,如梭杆菌属和Tyzzerella。这些发现揭示了肠道微生物如何在生活方式和疾病发展之间发挥隐藏的桥梁作用。我们的这些微生物介质的发现揭示了通过改变生活方式或在恶性转化之前针对这一致癌途径进行益生菌干预来预防HRA的新机会。临床试验本研究已在中国临床试验注册中心注册,注册号为ChiCTR1800015506。
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
mSystems
mSystems Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
10.50
自引率
3.10%
发文量
308
审稿时长
13 weeks
期刊介绍: mSystems™ will publish preeminent work that stems from applying technologies for high-throughput analyses to achieve insights into the metabolic and regulatory systems at the scale of both the single cell and microbial communities. The scope of mSystems™ encompasses all important biological and biochemical findings drawn from analyses of large data sets, as well as new computational approaches for deriving these insights. mSystems™ will welcome submissions from researchers who focus on the microbiome, genomics, metagenomics, transcriptomics, metabolomics, proteomics, glycomics, bioinformatics, and computational microbiology. mSystems™ will provide streamlined decisions, while carrying on ASM''s tradition of rigorous peer review.
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