A case–control study of the association between the gut microbiota and colorectal cancer: exploring the roles of diet, stress, and race

IF 4.3 3区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY Gut Pathogens Pub Date : 2024-03-11 DOI:10.1186/s13099-024-00608-w
Tiffany L. Carson, Doratha A. Byrd, Kristen S. Smith, Daniel Carter, Maria Gomez, Michael Abaskaron, Rebecca B. Little, Sh’Nese Townsend Holmes, William J. van Der Pol, Elliot J. Lefkowitz, Casey D. Morrow, Andrew D. Fruge
{"title":"A case–control study of the association between the gut microbiota and colorectal cancer: exploring the roles of diet, stress, and race","authors":"Tiffany L. Carson, Doratha A. Byrd, Kristen S. Smith, Daniel Carter, Maria Gomez, Michael Abaskaron, Rebecca B. Little, Sh’Nese Townsend Holmes, William J. van Der Pol, Elliot J. Lefkowitz, Casey D. Morrow, Andrew D. Fruge","doi":"10.1186/s13099-024-00608-w","DOIUrl":null,"url":null,"abstract":"The gut microbiota is associated with risk for colorectal cancer (CRC), a chronic disease for which racial disparities persist with Black Americans having a higher risk of CRC incidence and mortality compared to other groups. Given documented racial differences, the gut microbiota may offer some insight into previously unexplained racial disparities in CRC incidence and mortality. A case–control analysis comparing 11 women newly diagnosed with CRC with 22 cancer-free women matched on age, BMI, and race in a 1:2 ratio was conducted. Information about participants’ diet and perceived stress levels were obtained via 24-h Dietary Recall and Perceived Stress Scale-10 survey, respectively. Participants provided stool samples from which microbial genomic DNA was extracted to reveal the abundance of 26 genera chosen a priori based on their previously observed relevance to CRC, anxiety symptoms, and diet. Significantly lower alpha diversity was observed among cancer-free Black women compared to all other race-cancer status combinations. No group differences were observed when comparing beta diversity. Non-Hispanic White CRC cases tended to have higher relative abundance of Fusobacteria, Gemellaceae, and Peptostreptococcus compared to all other race-cancer combination groups. Perceived stress was inversely associated with alpha diversity and was associated with additional genera. Our findings suggest that microbiome-CRC associations may differ by racial group. Additional large, racially diverse population-based studies are needed to determine if previously identified associations between characteristics of the gut microbiome and CRC are generalizable to Black women and other racial, ethnic, and gender groups.","PeriodicalId":12833,"journal":{"name":"Gut Pathogens","volume":"156 1","pages":""},"PeriodicalIF":4.3000,"publicationDate":"2024-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Gut Pathogens","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1186/s13099-024-00608-w","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"GASTROENTEROLOGY & HEPATOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

The gut microbiota is associated with risk for colorectal cancer (CRC), a chronic disease for which racial disparities persist with Black Americans having a higher risk of CRC incidence and mortality compared to other groups. Given documented racial differences, the gut microbiota may offer some insight into previously unexplained racial disparities in CRC incidence and mortality. A case–control analysis comparing 11 women newly diagnosed with CRC with 22 cancer-free women matched on age, BMI, and race in a 1:2 ratio was conducted. Information about participants’ diet and perceived stress levels were obtained via 24-h Dietary Recall and Perceived Stress Scale-10 survey, respectively. Participants provided stool samples from which microbial genomic DNA was extracted to reveal the abundance of 26 genera chosen a priori based on their previously observed relevance to CRC, anxiety symptoms, and diet. Significantly lower alpha diversity was observed among cancer-free Black women compared to all other race-cancer status combinations. No group differences were observed when comparing beta diversity. Non-Hispanic White CRC cases tended to have higher relative abundance of Fusobacteria, Gemellaceae, and Peptostreptococcus compared to all other race-cancer combination groups. Perceived stress was inversely associated with alpha diversity and was associated with additional genera. Our findings suggest that microbiome-CRC associations may differ by racial group. Additional large, racially diverse population-based studies are needed to determine if previously identified associations between characteristics of the gut microbiome and CRC are generalizable to Black women and other racial, ethnic, and gender groups.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
肠道微生物群与结肠直肠癌关系的病例对照研究:探讨饮食、压力和种族的作用
肠道微生物群与结肠直肠癌(CRC)的发病风险有关,这种慢性疾病一直存在种族差异,与其他群体相比,美国黑人的 CRC 发病率和死亡率风险更高。鉴于有文献记载的种族差异,肠道微生物群可能会为以前无法解释的 CRC 发病率和死亡率的种族差异提供一些启示。我们进行了一项病例对照分析,将 11 名新诊断出患有 CRC 的女性与 22 名无癌症的女性按 1:2 的比例进行了年龄、体重指数和种族匹配。参与者的饮食信息和感知压力水平分别通过 24 小时饮食回忆和感知压力量表-10 调查获得。参与者提供粪便样本,从中提取微生物基因组 DNA,以揭示根据先前观察到的与 CRC、焦虑症状和饮食的相关性而预先选择的 26 个属的丰度。与所有其他种族-癌症状况组合相比,未患癌症的黑人妇女的α多样性明显较低。在比较贝塔多样性时,没有观察到任何群体差异。与所有其他种族-癌症状况组合相比,非西班牙裔白人 CRC 病例中的镰刀菌科、双子叶菌科和普氏链球菌的相对丰度较高。感知到的压力与阿尔法多样性成反比,并与其他菌属有关。我们的研究结果表明,微生物组与癌症的关系可能因种族群体而异。我们还需要进行更多基于种族的大型研究,以确定之前发现的肠道微生物组特征与 CRC 之间的关系是否适用于黑人妇女及其他种族、民族和性别群体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Gut Pathogens
Gut Pathogens GASTROENTEROLOGY & HEPATOLOGY-MICROBIOLOGY
CiteScore
7.70
自引率
2.40%
发文量
43
期刊介绍: Gut Pathogens is a fast publishing, inclusive and prominent international journal which recognizes the need for a publishing platform uniquely tailored to reflect the full breadth of research in the biology and medicine of pathogens, commensals and functional microbiota of the gut. The journal publishes basic, clinical and cutting-edge research on all aspects of the above mentioned organisms including probiotic bacteria and yeasts and their products. The scope also covers the related ecology, molecular genetics, physiology and epidemiology of these microbes. The journal actively invites timely reports on the novel aspects of genomics, metagenomics, microbiota profiling and systems biology. Gut Pathogens will also consider, at the discretion of the editors, descriptive studies identifying a new genome sequence of a gut microbe or a series of related microbes (such as those obtained from new hosts, niches, settings, outbreaks and epidemics) and those obtained from single or multiple hosts at one or different time points (chronological evolution).
期刊最新文献
Risk factors for peptic ulcer bleeding one year after the initial episode. Clonal and horizontal transmission of carbapenem-resistant Enterobacterales strains and genes via flies. Genomic characterisation of an extended-spectrum β-Lactamase-producing Klebsiella pneumoniae isolate assigned to a novel sequence type (6914). Occurrence and assemblage distribution of Giardia Duodenalis in symptomatic and asymptomatic patients in southeastern Iran (2019-2022). A triad of gut dysbiosis, dysregulated immunity, and 'leaky' gut characterize HCMV associated neonatal cholestasis.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1