L.R. Caley , A. Fuentes Balaguer , D. Bottomley , C. Young , L. Wilkinson , C. Sears , P. Quirke , D.G. Peckham
{"title":"WS04.05Faecal colorectal cancer-associated toxins in adults with cystic fibrosis: preliminary analysis","authors":"L.R. Caley , A. Fuentes Balaguer , D. Bottomley , C. Young , L. Wilkinson , C. Sears , P. Quirke , D.G. Peckham","doi":"10.1016/j.jcf.2025.03.514","DOIUrl":null,"url":null,"abstract":"<div><h3>Objectives</h3><div>Cystic fibrosis is associated with an increased risk of colorectal cancer (CRC) owing to a complex interplay between CFTR dysfunction, inflammation, gut dysbiosis and diet. Toxigenic bacteria in the gut of non-CF individuals have been implicated in CRC pathogenesis. We explored the presence of CRC-associated toxins in a cohort of adults with CF (awCF).</div></div><div><h3>Methods</h3><div>Baseline faecal samples from 80 awCF were tested for the presence of the following CRC associated bacteria and toxins: <em>Fusobacterium nucleatum</em>, FadA, NusG, <em>Escherichia coli</em>, polyketide synthase (<em>pks</em>), <em>Bacteroides fragilis</em> (BF) and Enterotoxigenic BF (ETBF) by employing Taqman qPCR in triplicate. In a subgroup, changes pre and post elexacaftor/tezacaftor/ivacaftor (ETI) were analysed (n=25).</div></div><div><h3>Results</h3><div>At baseline, median age was 34 years (IQR 28, 40), ppFEV<sub>1</sub> 53 (IQR 39, 74) with 34% participants being female. Percentage of FadA, NusG, <em>pks</em>, ETBF positive samples are displayed in Table 1.</div><div>In the pre and post ETI group, median time between samples and duration of ETI were 15 (IQR 14, 18) and 6 months (IQR 3,10) respectively. Changes in CRC-associated bacteria/toxins are presented in Table 1. Descriptively, there was no change in CRC-associated bacteria and toxins post ETI.</div></div><div><h3>Conclusion</h3><div>CRC-associated bacteria and toxins are present in CF stool samples and do not appear to change with short-term ETI therapy. Analysis in ongoing, including comparing levels to controls and CRC samples, to elucidate clinical implications of these findings.</div><div>Funded by the UK CF Trust (SRC 012)</div></div>","PeriodicalId":15452,"journal":{"name":"Journal of Cystic Fibrosis","volume":"24 ","pages":"Pages S8-S9"},"PeriodicalIF":5.4000,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Cystic Fibrosis","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1569199325006101","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"RESPIRATORY SYSTEM","Score":null,"Total":0}
引用次数: 0
Abstract
Objectives
Cystic fibrosis is associated with an increased risk of colorectal cancer (CRC) owing to a complex interplay between CFTR dysfunction, inflammation, gut dysbiosis and diet. Toxigenic bacteria in the gut of non-CF individuals have been implicated in CRC pathogenesis. We explored the presence of CRC-associated toxins in a cohort of adults with CF (awCF).
Methods
Baseline faecal samples from 80 awCF were tested for the presence of the following CRC associated bacteria and toxins: Fusobacterium nucleatum, FadA, NusG, Escherichia coli, polyketide synthase (pks), Bacteroides fragilis (BF) and Enterotoxigenic BF (ETBF) by employing Taqman qPCR in triplicate. In a subgroup, changes pre and post elexacaftor/tezacaftor/ivacaftor (ETI) were analysed (n=25).
Results
At baseline, median age was 34 years (IQR 28, 40), ppFEV1 53 (IQR 39, 74) with 34% participants being female. Percentage of FadA, NusG, pks, ETBF positive samples are displayed in Table 1.
In the pre and post ETI group, median time between samples and duration of ETI were 15 (IQR 14, 18) and 6 months (IQR 3,10) respectively. Changes in CRC-associated bacteria/toxins are presented in Table 1. Descriptively, there was no change in CRC-associated bacteria and toxins post ETI.
Conclusion
CRC-associated bacteria and toxins are present in CF stool samples and do not appear to change with short-term ETI therapy. Analysis in ongoing, including comparing levels to controls and CRC samples, to elucidate clinical implications of these findings.
期刊介绍:
The Journal of Cystic Fibrosis is the official journal of the European Cystic Fibrosis Society. The journal is devoted to promoting the research and treatment of cystic fibrosis. To this end the journal publishes original scientific articles, editorials, case reports, short communications and other information relevant to cystic fibrosis. The journal also publishes news and articles concerning the activities and policies of the ECFS as well as those of other societies related the ECFS.